EP1800312A2 - Surveillance dynamique de l'adhesion et de la diffusion cellulaire a l'aide du systeme rt-ces - Google Patents

Surveillance dynamique de l'adhesion et de la diffusion cellulaire a l'aide du systeme rt-ces

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Publication number
EP1800312A2
EP1800312A2 EP05812268A EP05812268A EP1800312A2 EP 1800312 A2 EP1800312 A2 EP 1800312A2 EP 05812268 A EP05812268 A EP 05812268A EP 05812268 A EP05812268 A EP 05812268A EP 1800312 A2 EP1800312 A2 EP 1800312A2
Authority
EP
European Patent Office
Prior art keywords
cell
impedance
cells
electrode
test
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP05812268A
Other languages
German (de)
English (en)
Other versions
EP1800312A4 (fr
Inventor
Yama A. Abassi
Josephine Atienza
Xiao Xu
Xiaobo Wang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Acea Biosciences Inc
Original Assignee
Yama A. Abassi
Josephine Atienza
Xiao Xu
Xiaobo Wang
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from PCT/US2004/037696 external-priority patent/WO2005047482A2/fr
Priority claimed from PCT/US2005/004481 external-priority patent/WO2005077104A2/fr
Priority claimed from US11/055,639 external-priority patent/US7560269B2/en
Priority claimed from PCT/US2005/027891 external-priority patent/WO2006015387A2/fr
Priority claimed from US11/198,831 external-priority patent/US8263375B2/en
Priority claimed from US11/197,994 external-priority patent/US7468255B2/en
Application filed by Yama A. Abassi, Josephine Atienza, Xiao Xu, Xiaobo Wang filed Critical Yama A. Abassi
Publication of EP1800312A2 publication Critical patent/EP1800312A2/fr
Publication of EP1800312A4 publication Critical patent/EP1800312A4/fr
Withdrawn legal-status Critical Current

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Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
    • G01N29/02—Analysing fluids
    • G01N29/036—Analysing fluids by measuring frequency or resonance of acoustic waves
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2291/00—Indexing codes associated with group G01N29/00
    • G01N2291/02—Indexing codes associated with the analysed material
    • G01N2291/025—Change of phase or condition
    • G01N2291/0256—Adsorption, desorption, surface mass change, e.g. on biosensors
    • G01N2291/0257—Adsorption, desorption, surface mass change, e.g. on biosensors with a layer containing at least one organic compound

Definitions

  • the present application relates to microelectronic devices and methods of use of to detect changes in impedance of a cell, and more specifically to microelectronic devices coated with biological molecules or organic compounds and methods of dynamically monitoring cell adhesion and cell monitoring.
  • ECM proteins extracellular matrix proteins
  • ECM proteins also play a prominent role during wound healing, and are involved in directing other cellular processes such as proliferation, survival, and differentiation. Failure of cells to interact with the appropriate biological surface or molecule can be detrimental to the faith of the cells and can contribute to cancer cell metastases.
  • the most widely used method is to apply the cells onto surfaces coated with appropriate ECM components, allow the cells to attach and adhere for a specified length of time and wash the unbound cells.
  • the attached cells are then fixed, labeled with fluorescent reagent such as rhodamine phalloidin and visualized using an epi-fluorescent microscope or an epi-fluorescent confocal microscope.
  • the cells can be labeled with a dye such as crystal violet and quantified by either counting the stained cells using a light microscope or solubilizing the stain and obtaining absorbance reading using a spectrophotometer.
  • Cells can also be pre-labeled with a fluorescent dye for live cells such as 6-carboxyfluorescein diacetate (CFDA) and then applied to appropriate ECM-coated surface. The unbound cells are washed off and the bound cells are quantified using a plate reader.
  • CFDA 6-carboxyfluorescein diacetate
  • An additional method for assessing the role of integrins and other adhesion proteins is to coat different surfaces with antibodies or peptides which are specific for the various receptors and then seed the cells which are expressing the appropriate integrin receptors. The interaction of integrin receptor on the cell surface with the antibody or peptide-coated surface will allow the cells to adhere and undergo specific morphological and biological changes which can then be assessed by using cell biological techniques discussed above.
  • each of the assays described are end-point assays which provide a "snapshot" of the adhesion process. All the assays involve pre-labeling or post-labeling of the cells and also involve fixation and permeabilization leading to destruction of the cell, hi this application we describe a label-free real-time assay using electronic cell sensor technology (RT-CES system) which addresses some of the major limitations of the current in vitro assays for assessing the interaction of bio-molecular coated surfaces with target cells. Furthermore, because the readout is non-invasive it precludes the need for fixation and lysis of the cells and allows for acquisition of information for biological events occurring after adhesion and spreading, such as proliferation and differentiation.
  • RT-CES system electronic cell sensor technology
  • the present invention includes a microlectronic cell sensor array including a non- conductive substrate, a plurality of electrode arrays positioned on the substrate, and a biological molecule or an organic compound, and optionally a control molecule or a control compound positioned on a portion of the substrate.
  • Each electrode array includes at least two electrodes and each electrode is separated from at least one adjacent electrode by an area of non-conductive material.
  • a method of coating a microelectronic cell sensor array with a biological molecule or organic compound is provided including providing a microelectronic cell sensor array and incubating a test solution on a first portion of the electrode array and optionally a control solution on a second portion of the electrode array.
  • the microelectronic cell sensor array may include a non-conductive substrate and a plurality of electrode arrays positioned on the substrate. Each electrode array may include at least two electrodes and each electrode may be separated from at least one adjacent electrode by an area of non-conductive material.
  • the test solution may include a biological molecule or organic compound and the control solution may include a vehicle control and optionally a control molecule or control compound. The incubation occurs under conditions suitable for attaching the biological molecule or organic compound to the electrode array or to the nonconductive substrate.
  • a method of monitoring cell adhesion or cell spreading including providing a microelectronic cell sensor array including a test portion and a control portion, coated at least in part with a biological molecule or organic compound and operably connected to an impedance analyzer.
  • a cell or cell population is introduced to the test portion and the control portion.
  • a series of impedance measurements of the test portion and the control portion are performed.
  • the change in impedance and optionally a cell index (CI) of the test portion and the change in impedance and optionally a cell index (CI) of the control portion is determined.
  • the change in impedance of the test portion is compared to the change in impedance of the control portion or alternatively the cell index (CI) of the test portion is compared to the cell index (CI) of the control portion. Cell adhesion or cell spreading occurs if the comparison demonstrates a.significant change in impedance.
  • a method of identifying a compound or biological molecule capable effecting cell adhesion or cell spreading including providing a microelectronic cell sensor array that is at least in part coated with a biological molecule or organic compound and is operably connected to an impedance analyzer, introducing a cell or cell population to a test portion and to a control portion of the microelectronic cell sensor array, performing a series of impedance measurements of the test portion and the control portion, determining the change in impedance and optionally a cell index (CI) of the test portion and the change in impedance and optionally a cell index (CI) of the control portion, comparing the change in impedance of the test portion to the change in impedance of the control portion or comparing the cell index (CI) of the test portion to the cell index (CI) of the control portion and determining cell adhesion or cell spreading is effected if the comparison demonstrates a significant change in impedance.
  • the substrate of the microelectronic cell sensor array is
  • a method of identifying an inhibitor of cell adhesion or cell spreading including providing a microlectronic cell sensor array operably connected to an impedance analyzer, the microelectronic cell sensor array including a non-conductive substrate, a plurality of electrode arrays positioned on the substrate, each electrode array including at least two electrodes, and each electrode is separated from at least one adjacent electrode by an area of non- conductive material and a biological molecule or organic compound positioned on the test portion of the substrate and on a control portion of the substrate.
  • the biological molecule or organic compound may be known to be capable of increasing cellular adhesion or cellular spreading.
  • the method also includes preincubating a cell or cell population with a biological molecule or compound suspected of being an effector or inhibitor of eel] spreading or cell adhesion defined as a test sample and preincubating a cell or cell population with a vehicle control defined as a control sample, introducing the test sample to the test portion and the control sample to the control portion, performing a series of impedance measurements of the test portion and the control portion, determining the change in impedance and optionally a cell index (CI) of the test portion and the change in impedance and optionally a cell index (CI) of the control portion, comparing the change in impedance of the test portion to the change in impedance of the control portion or comparing the cell index (CI) of the test portion to the cell index (CI) of the control portion, and determining cell adhesion or cell spreading is reduced or inhibited if the comparison demonstrates the change in impedance or cell index is greater in the control portion than the test portion.
  • FIG. 1 depicts a graphical representation of attachment and spreading of NTH3T3 cells on ACEA E-plates coated with fibronectin (FN) and poly-L-Lysine (PLL) and monitored by the RT-CES system.
  • the wells of ACEA E-plates were coated with 10 ⁇ g/mL FN or with 50 ⁇ g/mL PLL for 1 hour at 37 0 C.
  • the wells were washed with PBS prior to the addition of media alone for background recording.
  • NIH3T3 cells were added at a density of 10,000 cells per well and the adhesion and spreading of the cells were monitored by the RT-CES system.
  • FIG. 2 depicts images demonstrating attachment and spreading of NIH3T3 cells on 16X chamber slides coated with FN and PLL.
  • 16X chamber slides were coated with PLL and FN as described in FIG. 1.
  • NIH3T3 cells were added to the wells and at the indicated time points the cells were fixed and stained with rhodamine-phalloidin to stain the actin cytoskeleton. The cells were visualized and imaged with an epifluorescence microscope.
  • FIG. 3 depicts a graphical representation of the effect of FN concentration being coated onto the ACEA E-plate on NTH3T3 cell attachment and spreading.
  • ACEA E-plates were coated with increasing amounts of FN in the range of 0 ⁇ g/mL to 20 ⁇ g/mL.
  • 5000 NTH3T3 cells were added to the wells and the attachment and spreading of the cells were monitored by the RT-CES system.
  • the inset shows the average cell index of attachment at 3 hours in response to increasing amounts of FN.
  • FIG. 4 depicts a graphical representation of inhibition of cell attachment and spreading using the RGD containing peptides.
  • ACEA 16X E-plates were coated with FN as described in FIG. 1.
  • NTH3T3 cells were preincubated for 30 minutes with the indicated final concentration of the peptide GRGDS and also with the indicated concentration of the control peptide (GRADSP). The cells were added to E-plates coated with FN and the attachment and spreading of NIH3T3 cells were monitored by the RT-CES system.
  • FIG. 5 depicts a graphical representation of attachment and spreading of Jurkat T cells on ACEA E-plates coated with anti-CD-3 antibody.
  • E-plates were coated with lO ⁇ g/mL of 0KT3 antibody (anti-CD-3) or a control antibody for 2 hours at room temperature.
  • the wells were washed with PBS and then the background impedance determined using the RT-CES. 500,000 Jurkat T cells were added per well and the attachment and spreading of the cells were monitored using the RT-CES system.
  • FIG. 6 depicts (A) Dynamic monitoring of cell attachment and spreading on PLL and FN-coated surfaces using the RT-CES system. (B) The RT-CES measurements correlate with the extent of cell attachment and spreading using conventional phalloidin staining of the actin cytoskeleton and immunofluorescence microscopy.
  • FIG 7 depicts (A) Quantitative and dynamic monitoring of cell attachment and spreading in response to increasing concentrations of FN using the RT-CES system. (B) Comparison of ACEA units of Cell Index versus manual counting of the cells for different FN concentrations at 3 hours.
  • FIG. 8 depicts (A) Dose-dependent inhibition of cell attachment and spreading in response to cyclic-RGD peptides, using the RT-CES system. (B) Comparison of cell attachment and spreading in response to a control peptide and cyclic-RGD peptides at three hours.
  • FIG. 9 depicts (A) Dynamic monitoring of the dose-dependent effect of Latriculin on NIH3T3 cell attachment and spreading on FN-coated wells, using the RT-CES system (B) Analysis of the dose-dependent effect of Latriculin on NTH3T3 cell attachment and spreading at two hours.
  • FIG. 10 depicts (A) Dynamic monitoring of the effect of the Src inhibitor, PP2 on BxPC3 cell attachment and spreading on FN, using the RT-CES system. (B) Comparison of the extent of cell attachment and spreading on FN in response to PP2 compared to DMSO control at two hours.
  • FIG. 11 depicts (A) Dynamic monitoring of cell attachment and spreading using the RT- CES system of BxPC3 cells transfected with an siRNA specific for c-Src or a control siRNA. (B) Comparison of the extent of cell attachment and spreading of BxPC3 cells transfected with c-Src siRNA or a control siRNA at two hours.
  • a " or “an” means “at least one” or “one or more. " As used herein, “membrane " is a sheet of material.
  • biocompatible membrane means a membrane that does not have deleterious effects on cells, including the viability, attachment, spreading, motility, growth, or cell division.
  • a “biomolecular coating " ' or a “'biological molecule coating” is a coating on a surface that comprises a molecule that is a naturally occurring biological molecule or biochemical, or a biochemical derived from or based on one or more naturally occurring biomolecules or biochemicals.
  • a biological molecule coating can include an extracellular matrix component (e.g., fibronectin, collagens), or a derivative thereof, or can comprise a biochemical such as polylysine or polyornithine, which are polymeric molecules based on the naturally occurring biochemicals lysine and ornithine.
  • a biochemical such as polylysine or polyornithine, which are polymeric molecules based on the naturally occurring biochemicals lysine and ornithine.
  • Polymeric molecules based on naturally occurring biochemicals such as amino acids can use isomers or enantiomers of the naturally-occuring biochemicals.
  • organic compound coating is a coating on a surface that includes an organic compound.
  • an organic compound may include a natural ligand or an agonist or an antagonist for a cell surface receptor.
  • extracellular matrix component is a molecule that occurs in the extracellular matrix of an animal. It can be a component of an extracellular matrix from any species and from any tissue type. Nonlimiting examples of extracellular matrix components include laminins, collagens fibronectins, other glycoproteins, peptides, glycosaminoglycans, proteoglycans, etc. Extracellular matrix components can also include growth factors.
  • Electrode is a structure having a high electrical conductivity, that is, an electrical conductivity much higher than the electrical conductivity of the surrounding materials.
  • an “electrode structure” refers to a single electrode, particularly one with a complex structure (as, for example, a spiral electrode structure), or a collection of at least two electrode elements that are electrically connected together. All the electrode elements within an “electrode structure "" are electrically connected.
  • electrode element refers to a single structural feature of an electrode structure, such as. for example, a fingerlike projection of an interdigitated electrode structure.
  • an “electrode array” or “electrode structure unit” is two or more electrode structures that are constructed to have dimensions and spacing such that they can, when connected to a signal source, operate as a unit to generate an electrical field in the region of spaces around the electrode structures.
  • Preferred electrode structure units of the present invention can measure impedance changes due to cell attachment to an electrode surface.
  • Non-limiting examples of electrode structure units are interdigitated electrode structure units and concentric electrode structure units.
  • Electrode bus is a portion of an electrode that connects individual electrode elements or substructures.
  • An electrode bus provides a common conduction path from individual electrode elements or individual electrode substructures to another electrical connection.
  • an electrode bus can contact each electrode element of an electrode structure and provide an electrical connection path to electrical traces that lead to a connection pad.
  • Electrode traces or “electrically conductive traces” or “electrical traces”, are electrically conductive paths that extend from electrodes or electrode elements or electrode structures toward one end or boundary of a device or apparatus for connecting the electrodes or electrode elements or electrode structures to an impedance analyzer.
  • the end or boundary of a device may correspond to the connection pads on the device or apparatus.
  • connection pad is an area on an apparatus or a device of the present invention which is electrically connected to at least one electrode or all electrode elements within at least one electrode structure on an apparatus or a device and which can be operatively connected to external electrical circuits (e.g., an impedance measurement circuit or a signal source).
  • external electrical circuits e.g., an impedance measurement circuit or a signal source.
  • the electrical connection between a connection pad and an impedance measurement circuit or a signal source can be direct or indirect, through any appropriate electrical conduction means such as leads or wires.
  • Such electrical conduction means may also go through electrode or electrical conduction paths located on other regions of the apparatus or device.
  • Interdigitated means having projections coming one direction that interlace -with projections coming from a different direction in the manner of the fingers of folded hands (with the caveat that interdigitated electrode elements preferably do not contact one another).
  • a "'high probability of contacting an electrode element” means that, if a cell is randomly positioned within the sensor area of a device or apparatus of the present invention, the probability of a cell (or particle) contacting on an electrode element, calculated from the average diameter of a cell used on or in a device or apparatus of the present invention, the sizes of the electrode elements, and the size of the gaps between electrode elements, is greater than about 50%, more preferably greater than about 60%, yet more preferably greater than about 70%, and even more preferably greater than about 80%, greater than about 90%, or greater than about 95%.
  • At least two electrodes fabricated on said substrate means that the at least two electrodes are fabricated or made or produced on the substrate.
  • the at least two electrodes can be on the same side of the substrate or on the different side of the substrate.
  • the substrate may have multiple layers, the at least two electrodes can be either on the same or on the different layers of the substrate.
  • At least two electrodes fabricated to a same side of said substrate means that the at least two electrodes are fabricated on the same side of the substrate.
  • At least two electrodes fabricated to a same plane of said substrate means that, if the nonconducting substrate has multiple layers, the at least two electrodes are fabricated to the same layer of the substrate.
  • said . . . electrodes (or electrode structures) have substantially the same surface area means that the surface areas of the electrodes referred to are not substantially different from each other, so that the impedance change due to cell attachment or growth on any one of the electrodes (or electrode structures) referred to will contribute to the overall detectable change in impedance to a same or similar degree as the impedance change due to cell attachment or growth on any other of the electrodes (or electrode structures) referred to.
  • an ⁇ ' one of the electrodes can contribute to overall change in impedance upon cell attachment or growth on the electrode.
  • the ratio of surface area between the largest electrode and the smallest electrode that have “substantially the same surface area " is less than 10.
  • the ratio of surface area between the largest electrode and the smallest electrode of an electrode array is less than 5, 4, 3 , 2, 1.5, 1.2 or 1 1.
  • the at least two electrodes of an electrode structure have nearly identical or identical surface area.
  • said device has a surface suitable for cell attachment or growth
  • the electrode and/or non-electrode area of the apparatus has appropriate physical, chemical or biological properties such that cells of interest can viably attach on the surface and new cells can continue to attach, while the cell culture grows, on the surface of the apparatus.
  • the device, or the surface thereof contain substances necessary for cell viability or growth. These necessary substances, e.g., nutrients or growth factors, can be supplied in a medium.
  • a suspension of viable, unimpaired, epithelial or endothelial cells is added to the "surface suitable for cell attachment" when at least 50% of the cells are adhering to the surface within twelve hours.
  • a surface that is suitable for cell attachment has surface properties so that at least 70% of the cells are adhering to the surface within twelve hours of plating (i.e., adding cells to the chamber or well that comprises the said device). Even more preferably, the surface properties of a surface that is suitable for cell attachment results in at least 90% of the cells adhering to the surface within twelve hours of plating. Most preferably, the surface properties of a surface that is suitable for cell attachment results in at least 90% of the cells adhering to the surface within eight, six, four, two hours of plating.
  • detecttable change in impedance between or among said electrodes means that the impedance between or among said electrodes (or electrode structures) would have a significant change that can be detected by an impedance anah'zer or impedance measurement circuit when molecule binding reaction occurs on the electrode surfaces.
  • the impedance change refers to the difference in impedance values when molecule binding reaction occurs on the electrode surface of the apparatus and when no molecular reaction occurs on the electrode surface.
  • the impedance change refers to the difference in impedance values when cells are attached to the electrode surface and when cells are not attached to the electrode surface, or when the number, type, activity, adhesiveness, or morphology of cells attached to the electrode- comprising surface of the apparatus changes.
  • the change in impedance is larger than 0.1% to be detectable.
  • the detectable change in impedance is larger than 1%, 2%, 5%, or 8%. More preferably, the detectable change in impedance is larger than 10%.
  • Impedance between or among electrodes is typically a function of the frequency of the applied electric field for measurement. "Detectable change in impedance between or among said electrodes" does not require the impedance change at all frequencies being detectable.
  • Detectable change in impedance between or among said electrodes only requires a detectable change in impedance at any single frequency (or multiple frequencies).
  • impedance has two components, resistance and reactance (reactance can be divided into two categories, capacitive reactance and inductive reactance).
  • Detectable change in impedance between or among said electrodes requires only that either one of resistance and reactance has a detectable change at any single frequency or multiple frequencies.
  • impedance is the electrical or electronic impedance.
  • the method for the measurement of such impedance is achieved by, (1) applying a voltage between or among said electrodes at a given frequency (or multiple frequencies, or having specific voltage waveform) and monitoring the electrical current through said electrodes at the frequency (or multiple frequencies, or having specific waveform), dividing the voltage amplitude value by the current amplitude value to derive the impedance value; (2) applying an electric current of a single frequency component (or multiple frequencies or having specific current wave form) through said electrodes and monitoring the voltage resulted between or among said electrodes at the frequency (or multiple frequencies, or having specific waveform), dividing the voltage amplitude value by the current amplitude value to derive the impedance value; (3) other methods that can measure or determine electric impedance.
  • said at least two electrodes have substantially different surface area
  • the surface areas of any electrodes are not similar to each other so that the impedance change due to cell attachment or growth on the larger electrode will not contribute to the overall detectable impedance to a same or similar degree as the impedance change due to cell attachment or growth on the smaller electrodes.
  • any impedance change due to cell attachment or growth on the larger electrode is significantly smaller than the impedance change due to cell attachment or growth on the smaller electrode.
  • the ratio of surface area between the largest electrode and the smallest electrode is more than 10.
  • the ratio of surface area between the largest electrode and the smallest electrode is more than 20, 30, 40, 50 or 100.
  • multiple pairs of electrodes or electrode structures spatially arranged according to wells of a multi-well microplate means that the multiple pairs of electrodes or electrode structures of a device or apparatus are spatially arranged to match the spatial configuration of wells of a multi-well microplate so that, when desirable, the device can be inserted into, joined with, or attached to a multiwell plate (for example, a bottomless multiwell plate) such that multiple wells of the multi-well microplate will comprise electrodes or electrode structures.
  • arranged in a row-column configuration means that, in terms of electric connection, the position of an electrode, an electrode array or a switching circuit is identified by both a row position number and a column position number.
  • each well contains substantially same number . . . of cells
  • the lowest number of cells in a well is at least 50% of the highest number of cells in a well.
  • the lowest number of cells in a well is at least 60%, 70%, 80%, 90%, 95% or 99% of the highest number of cells in a well. More preferably, each well contains an identical number of cells.
  • each well contains same type of mammalian cells : e.g., human cells, or different mammalian cells, e.g.. human cells as well as other non-human mammalian cells such as mice, goat or monkey cells, etc.
  • each well contains . . . serially different concentration of a test compound
  • each well contains a test compound with a serially diluted concentrations, e.g. , an one-tenth serially diluted concentrations of 1 M, 0.1 M, 0.01 M, etc.
  • dose-response curve means the dependent relationship of response of cells on the dose concentration of a test compound.
  • the response of cells can be measured by many different parameters. For example, a test compound is suspected to have cytotoxicity and cause cell death. Then the response of cells can be measured by percentage of non- viable (or viable) cells after the cells are treated by the test compound. Plotting this percentage of non-viable (or viable) cells as a function of the does concentration of the test compound constructs a dose response curve. In the present application, the percentage of non-viable (or viable) cells can be expressed in terms of measured impedance values, or in terms of cell index derived from impedance measurement, or in terms of cell change indexes.
  • cell index can be shown to have a linear correlation or positive correlation with the number of viable cells in a well from which cell index was derived from the impedance measurement.
  • dose-response curve the dose-response curve
  • cell index not only correlate with the number of viable cells in the wells but also relate to the cell morphology and cell attachment.
  • plotting cell index versus doss concentration provides information not only about number of cells but also about their physiological status (e.g. cell morphology and cell adhesion).
  • the electrodes have, along the length of the microchannel. a length that is substantially less than the largest single-dimension of a particle to be analyzed " means that the electrodes have, along the length of the microchannel, a length that is at least less than 90% of the largest single-dimension of a particle to be analyzed.
  • the electrodes have, along the length of the microchannel, a length that is at least less than 80%, 70%, 60%, 50%, 40%, 30%, 20%, 10%, 5% of the largest single- dimension of a particle to be analyzed.
  • an aperture having a pore size that equals to or is slightly larger than size of said particle means that aperture has a pore size that at least equals to the particle size but less than 300% of the particle size.
  • both pore size and particle size are measured in terms of single dimension value.
  • microelectrode strip or electrode strip means that a non ⁇ conducting substrate strip on which electrodes or electrode structure units are fabricated or incorporated.
  • the non-limiting examples of the non-conducting substrate strips include polymer membrane, glass, plastic sheets, ceramics, insulator-on-semiconductor, fiber glass (like those for manufacturing printed-circuits-board).
  • Electrode structure units having different geometries can be fabricated or made on the substrate strip by any suitable microfabrication, micromachining, or other methods.
  • Non-limiting examples of electrode geometries include interdigitated electrodes, circle-on-line electrodes, diamond- on-line electrodes, castellated electrodes, or sinusoidal electrodes.
  • Characteristic dimensions of these electrode geometries may vary from as small as less than 5 micron, or less than 10 micron, to as large as over 200 micron, over 500 micron, over 1 mm.
  • the characteristic dimensions of the electrode geometries refer to the smallest width of the electrode elements, or smallest gaps between the adjacent electrode elements, or size of a repeating feature on the electrode geometries.
  • the microelectrode strip can be of any geometry for the present invention.
  • One exemplar ⁇ 7 geometry for the microelectrode strips is rectangular shape - having the width of the strip between less than 50 micron to over 10 mm. and having the length of the strip between less than 60 micron to over 15 mm.
  • An exemplar ⁇ ' geometry of the microelectrode strips may have a geometry having a width of 200 micron and a length of 20 mm.
  • a single microelectrode strip may have two electrodes serving as a measurement unit, or multiple such two-electrodes serving as multiple measurement units, or a single electrode structure unit as a measurement unit, or multiple electrode structure units serving as multiple electrode structure units.
  • these electrode structure units are positioned along the length direction of the strip.
  • the electrode structure units may be of squared-shape, or rectangular-shape, or circle shapes. Each of electrode structure units may occupy size from less than 50 micron by 50 micron, to larger than 2 mm x 2mm.
  • sample refers to anything which may contain a moiety to be isolated, manipulated, measured, quantified, detected or analyzed using apparatuses, microplates or methods in the present application.
  • the sample may be a biological sample, such as a biological fluid or a biological tissue.
  • biological fluids include suspension of cells in a medium such as cell culture medium, urine, blood, plasma, serum, saliva, semen, stool, sputum, cerebral spinal fluid, tears, mucus, amniotic fluid or the like.
  • Biological tissues are aggregates of cells, usually of a particular kind together with their intercellular substance that form one of the structural materials of a human, animal, plant, bacterial, fungal or viral structure, including connective, epithelium, muscle and nerve tissues.
  • biological tissues also include organs, tumors, lymph nodes, arteries and individual cell(s).
  • the biological samples may further include cell suspensions, solutions containing biological molecules (e.g. proteins, enzymes, nucleic acids, carbohydrates, chemical molecules binding to biological molecules) .
  • biological molecules e.g. proteins, enzymes, nucleic acids, carbohydrates, chemical molecules binding to biological molecules
  • a “liquid (fluid) sample” refers to a sample that naturally exists as a liquid or fluid, e.g., a biological fluid.
  • a “liquid sample” also refers to a sample that naturally exists in a non-liquid status, e.g.. solid or gas. but is prepared as a liquid, fluid. solution or suspension containing the solid or gas sample material.
  • a liquid sample can encompass a liquid, fluid, solution or suspension containing a biological tissue.
  • a “compound " or "test compound” is any compound whose activity or direct or indirect effect or effects on cells is investigated in any assay.
  • a test compound can be any compound, including, but not limited to, a small molecule, a large molecule, a molecular complex, an organic molecule, an inorganic molecule, a biomolecule or biological molecule such as but not limited to a lipid, a steroid, a carbohydrate, a fatty acid, an amino acid, a peptide, a protein, a nucleic acid, or any combination thereof.
  • a test compound can be a synthetic compound, a naturally occurring compound, a derivative of a naturally-occurring compound, etc. The structure of a test compound can be known or unknown.
  • a compound is capable of, or is suspected of, effecting cell adhesion or cell spreading.
  • a compound is capable of, or is suspected of, stimulating or inhibiting cell adhesion or cell spreading.
  • a compound is capable of, or is suspected of, interacting with cells (for example, binding to cell surface receptor, or inhibiting certain intracellular signal transduction pathway, or activating cells).
  • a "known compound” is a compound for which at least one activity is known.
  • a known compound preferably is a compound for which one or more direct or indirect effects on cells is known.
  • the structure of a known compound is known, but this need not be the case.
  • the mechanism of action of a known compound on cells is known, for example, the effect or effects of a known compound on cells can be, as nonlimiting examples, effects on cell viability, cell adhesion, apoptosis, cell differentiation, cell proliferation, cell morphology, cell cycle, IgE-mediated cell activation or stimulation, receptor-ligand binding, cell number, cell quality, cell cycling, cell adhesion, cell spreading, etc.
  • impedance value is the impedance measured for electrodes in a well with or without cell present. Impedance is generally a function of the frequency, i.e., impedance values depend on frequencies at which the measurement was conducted. For the present application, impedance value refers to impedance measured at either single frequency or multiple frequencies. Furthermore, impedance has two components, one resistance component and one reactance component. Impedance value in the present application refers to resistance component, or reactance component, or both resistance and reactance component. Thus, when “impedance value " was measured or monitored, we are referring to that, resistance, or reactance, or both resistance and reactance were measured or monitored. In many embodiments of the methods of the present application, impedance values also refer to parameter values that are derived from raw, measured impedance data. For example, cell index, or normalized cell index, or delta cell index could be used to represent impedance values.
  • a "Cell Index” or “CI” is a parameter that can derived from measured impedance values and that can be used to reflect the change in impedance values. There are a number of methods to derive or calculate Cell Index.
  • a “Normalized Cell Index” at a given time point is calculated by dividing the Cell Index at the time point by the Cell Index at a reference time point. Thus, the Normalized Cell Index is 1 at the reference time point.
  • a “delta cell index” at a given time point is calculated by subtracting the cell index at a standard time point from the cell index at the given time point. Thus, the delta cell index is the absolute change in the cell index from an initial time (the standard time point) to the measurement time.
  • a "Cell Change Index” or "CCI” is a parameter derived from Cell Index and "CCI" at a time point is equal to the 1 st order derive of the Cell Index with respect to time, divided by the Cell Index at the time point. In other words, CCI is calculated as
  • target cell refers to any cell that is to be monitored for adhesion or spreading.
  • Non-limiting examples of target cells include eukaryotic or prokaryotic cells of interest.
  • Eukaryotic cells of particular interest may be human cells, a human cell population or a human cell line.
  • Immune cells may be utilized such as B-lymphocytes, T-lymphocytes Natural Killer (NK) cells. Cytotoxic T- Lymphocytes (CTLs), neutrophils, easonophils : macrophages. Natural Killer T (NKT) cells. PBMCs and the like.
  • primary cell or “primary cells” refers to any non-immortalized cell that has been derived from various tissues and organs of a patient or an animal.
  • the present invention includes devices for measuring cell-substrate impedance that comprise a nonconducting substrate; two or more electrode arrays fabricated on the substrate, where each of the two or more electrode arrays comprises two electrode structures; and at least two connection pads, each of which is located on an edge of the substrate.
  • Each electrode array of the device may have approximately uniform electrode resistance across the entire array.
  • the substrate of the device has a surface suitable for attaching a biological molecule or organic compound (such as covalently or noncovelently bonding).
  • the substrate may also be suitable for a attaching a cell where cell attachment or spreading on the substrate can result in a detectable change in impedance between or among the electrode structures within each electrode array.
  • An electrode array is two or more electrode structures that are constructed to have dimensions and spacing such that they can, when connected to a signal source, operate as a unit to generate an electrical field in the region of spaces around the electrode structures.
  • An electrode structure refers to a single electrode, particularly one with a complex structure. (For example, an electrode structure can comprise two or more electrode elements that are electrically connected together.)
  • an electrode array comprises two electrode structures, each of which comprises multiple electrode elements, or substructures.
  • the electrode structures of each of the two or more electrode arrays of a device have substantially the same surface area, hi preferred embodiments of a device of the present invention, each of the two or more electrode arrays of a device comprise two electrode structures, and each electrode structure comprises multiple electrode elements.
  • Each of the two electrode structures of an electrode array is connected to a separate connection pad that is located at the edge of the substrate.
  • the first of the two electrode structures is connected to one of the two or more connection pads
  • the second of the two electrode structures is connected to another of the two or more connection pads.
  • each array of a device is individually addressed, meaning that the electrical traces and connection pads of the arrays are configured such that an array can be connected to an impedance analyzer in such a way that a measuring voltage can be applied across a single array at a given time by using switches (such as electronic switches).
  • Each electrode array of the device has an approximately uniform electrode resistance distribution across the entire array.
  • uniform resistance distribution across the array is meant that when a measurement voltage is applied across the electrode structures of the array, the electrode resistance at any given location of the array is approximately equal to the electrode resistance at any other location on the array.
  • the electrode resistance at a first location on an array of the device and the electrode resistance at a second location on the same array does not differ by more than 30%. More preferably, the electrode resistance at a first location on an array of the device and the electrode resistance at a second location on the same array does not differ by more than 15%. Even more preferably, the electrode resistance at a first location on an array of the device and a second location on the same array does not differ by more than 5%. More preferably yet, the electrode resistance at a first location on an array of the device and a second location on the same array does not differ by more than 2%.
  • the electrode elements For a device of the present invention, preferred arrangements for the electrode elements, gaps between the electrodes and electrode buses in a given electrode array are used to allow all cells, no matter where they land and attach to the electrode surfaces, to contribute similarly to the total impedance change measured for the electrode array.
  • the field strength is related to the potential difference between the nearest point on a first electrode structure of the array and the nearest point on a second electrode structure of the array. It is therefore desirable to have similar electric potential drops across the electrode elements and across the electrode buses of a given array.
  • the electrode resistance at a location of interest is equal to the sum of the electrode resistance between the nearest point on a first electrode structure (that is the point on the first electrode structure nearest the location of interest) and a first connection pad connected to the first electrode structure and the electrode resistance between the nearest point on a second electrode structure (that is the point on the first electrode structure nearest the location of interest) and a second connection pad connected to the second electrode structure.
  • Devices of the present invention are designed such that the arrays of the device have an approximately uniform distribution across the whole array. This can be achieved, for example, by having electrode structures and electrode buses of particular spacing and dimensions (lengths, widths, thicknesses and geometrical shapes) such that the resistance at any single location on the array is approximately equal to the resistance at any single other location on the array.
  • the electrode elements (or electrode structures) of a given array will have even spacing and be of similar thicknesses and widths
  • the electrode buses of a given array will be of similar thicknesses and widths
  • the electrode traces leading from a given array to a connection pad will be of closely similar thicknesses and widths.
  • an array is designed such that the lengths and geometrical shapes of electrode elements or structures, the lengths and geometrical shapes of electrode traces, and the lengths and geometrical shapes of buses allow for approximately uniform electrode resistance distribution across the array.
  • electrode structures comprise multiple electrode elements, and each electrode element connects directly to an electrode bus. Electrode elements of a first electrode structure connect to a first electrode bus, and electrode elements of a second electrode structure connect to a second electrode bus. In these embodiments, each of the two electrode buses connects to a separate connection pad via an electrical trace. Although the resistances of the traces contribute to the resistance at a location on the array, for any two locations on the array the trace connections from the first bus to a first connection pad and from the second bus to a second connection pad are identical. Thus, in these
  • trace resistances do not need to be taken into account in designing the geometry of the array to provide for uniform resistances across the array.
  • a device for monitoring cell- substrate impedance has two or more electrode arrays that share a connection pad.
  • one of the electrode structures of at least one of the electrode arrays of the device is connected to a connection pad that also connects to an electrode structure of at least one other of the electrode arrays of the device.
  • each of the two or more arrays has a first electrode structure connected to a connection pad that connects with an electrode structure of at least one other electrode array, and each of the two or more arrays has a second electrode structure that connects to a connection pad that does not connect with any other electrode structures or arrays of the device.
  • each of the electrode structures of an array is connected to an electrode bus that is connected to one of the two or more connection pads of the device via an electrically conductive trace.
  • each of the two electrode structures is connected to a single bus, such that each array connects to two buses, one for each electrode structures. In this arrangement, each of the two buses connects to a separate connection pad of the substrate.
  • the electrically conductive traces that connect a bus with a connection can be fabricated of any electrically conductive material.
  • the traces can be localized to the surface of the substrate, and can be optionally covered with an insulating layer. Alternatively the traces can be disposed in a second plane of the substrate. Description of arrangements and design of electrically conductive traces on impedance measurement devices can be found in parent U.S. Patent Application 10/705,447, herein incorporated by reference for all disclosure on fabrication and design of electrically conductive trace on substrates.
  • Appropriate electronic connection means such as metal clips engaged onto the connection pads on the substrate and connected printed-circuit-boards can be used for leading the electronic connections from the connection pads on the devices to external
  • ID electronic circuitry e.g. an impedance analyzer. Description of the design of cell- substrate impedance devices and their manufacture can be found in U.S. Patent Application No. 10/705.447. herein incorporated by reference for all description and disclosure of the design, features, and manufacture of impedance device comprising electrode arrays.
  • the nonconducting substrate is planar, and is flat or approximately flat.
  • Exemplary substrates can comprise many materials, including, but not limited to, silicon dioxide on silicon, silicon-on-insulator (SOI) wafer, glass (e.g., quartz glass, lead glass or borosilicate glass), sapphire, ceramics, polymer, fiber glass, plastics, e.g., polyimide (e.g. Kapton, polyimide film supplied by DuPont), polystyrene, polycarbonate, polyvinyl chloride, polyester, polypropylene and urea resin.
  • the substrate and the surface of the substrate are not going to interfere with molecular binding reactions that will occur at the substrate surface.
  • any surface of the nonconducting substrate that can be exposed to cells during the use of a device of the present invention is preferably biocompatible.
  • Substrate materials that are not biocompatible can be made biocompatible by coating with another material, such as polymer or biomolecular coating.
  • All or a portion of the surface of a substrate can be chemically treated, including but not limited to, modifying the surface such as by addition of functional groups, or addition of charged or hydrophobic groups.
  • a portion of the surface of the substrate is modified to display a biological molecule or organic compound of interest.
  • biological molecules or organic compounds that may be desired include those that are involved or may be involved in cell adhesion or cell spreading.
  • the present invention includes a variety of biological molecules and organic compounds including a DNA molecule, an RNA molecule, a protein, a polypeptide and oligopeptide and the like.
  • Molecules of particular interest may include an antibody, a ligand, a peptide, a receptor, one or more proteins or compounds present in the extracellular matrix (ECM), a molecule or compound capable of binding an mtegrin. a cell surface receptor and the like.
  • ECM extracellular matrix
  • a peptide such as an arginine-glycine-aspartic acid (RGD) motif or some form thereof is the biological molecule.
  • the present invention also includes organic compounds that are agonists or antagonists for a cell surface receptor involved in cell adhesion, including integrins, growth factor receptors. E-cadherins. N-cadherins. PECAMS and ICAMS.
  • the modification may ultimately result in a coated surface or a surface that is coated at least in part with a biological molecule or organic compound.
  • the coated portion may represent a first portion, a second portion and the like.
  • the region may also be referred to as a test portion or a control portion depending on the assay.
  • an inner surface of the wells may be coated at least in part with a biological molecule or organic compound.
  • the biological molecule or organic compound may interact with the substrate in any suitable fashion that would result in display of a biological molecule or organic compound.
  • the biological molecule or organic compound may be covalently bound, ionically bound, bound by Van der Waals forces and the like to the substrate or electrode.
  • the biological molecule or organic compound may be attached directly to the substrate or electrode or may be attached via an intermediate structure.
  • a biological molecule or compound may be bound by incubating the molecule or compound in a suitable medium such as phosphate buffered saline (PBS), borate buffered saline (BBS) and the like.
  • PBS phosphate buffered saline
  • BSS borate buffered saline
  • an intermediate such as poly-L-lysine may be applied to the substrate then attached to the biological molecule or organic compound.
  • electrode arrays for devices of the present invention include arrays comprising two electrode structures, such as, for example, spiral electrode arrays and interdigitated arrays.
  • electrode arrays are fabricated on a substrate, in which the arrays comprises two electrode structures, each of which comprises multiple circle-on-line electrode elements, in which the electrode elements of one structure alternate with the electrode elements of the opposite electrode structure.
  • the electrode elements (or electrode structures) of an array of the present device of the present-invention are of approximately equal widths.
  • the electrode elements (or electrode structures) of an array of the present device of the present invention are greater than 30 microns in width, more preferably from about 50 to about 300 microns in width, and more preferably yet about 90 microns in width.
  • the electrode elements (or electrode structures) of an array of the present device of the present invention are approximately evenly spaced.
  • the gap between electrode elements (or electrode structures) of an array of the present device of the present invention is less than 50 microns in width, more preferably from about 5 to about 30 microns in width, and more preferably yet about 20 microns in width.
  • a device of the present invention can include one or more fluid-impermeable receptacles which serve as fluid containers. Such receptacles may be reversibly or irreversibly attached to or formed within the substrate or portions thereof (such as, for example, wells formed as in a microtiter plate).
  • the device of the present invention includes microelectrode strips reversibly or irreversibly attached to plastic housings that have openings that correspond to electrode structure units located on the microelectrode strips.
  • Suitable fluid container materials comprise plastics, glass, or plastic coated materials such as ceramics, glass, metal, etc. Descriptions and disclosure of devices that comprise fluid containers can be found in parent U.S. Patent Application No. 10/705,447, herein incorporated by reference for all disclosure of fluid containers and fluid container structures that can engage a substrate comprising electrodes for impedance measurements, including their dimensions, design, composition, and methods of manufacture.
  • each electrode array on the substrate of a device of the present invention is associated with a fluid-impermeable container or receptacle, such as, for example, a well.
  • the device of the present invention is assembled to a bottomless, multiwell plastic plate or strip with a fluid tight seal.
  • the device is assembled such that a single array of the substrate is at the bottom of a receptacle or well.
  • each array of a device is associated with a well of a multiwell plate, hi some preferred embodiments, a multiwell device for cell-substrate impedance measurement has "non-array" wells that are attached to the substrate but not associated with arrays. Such wells can optionally be used for performing non-impedance based assays, or for viewing cells microscopically.
  • a device of the present invention preferably has between 2 and 1,536 wells, more preferably between 4 and 384 wells, and even more preferably, between 16 and 96 wells, all or less than all or which are associated with electrode arrays.
  • commercial tissue culture plates can be adapted to fit a device of the present invention. Bottomless plates may also be custom-made to preferred dimensions.
  • well diameters are from about 1 millimeter to about 20 millimeters, more preferably from about 2 millimeters to about 8 millimeters at the bottom of the well (the end disposed on the substrate).
  • the wells can have a uniform diameter or can taper toward the bottom so that the diameter of the container at the end in contact with the substrate is smaller than the diameter of the opposing end.
  • the present invention also includes methods of using a device of the present invention that comprises fluid containers situated over electrode arrays to measure cell- substrate impedance.
  • Such methods include: providing a device of the present invention optionally including wells or fluid chambers situated over electrode arrays, coating at least in part the substrate or optionally the wells with a biological molecule or organic compound, attaching an impedance analyzer to a device of the present invention, adding cells to one or more fluid containers of the device, and measuring impedance over one or more arrays of the device.
  • Methods of performing cell assays using impedance measurement devices can be found in parent U.S. Patent Application No. 10/987,732 and U.S. Patent Application 10/705,447, both herein incorporated by reference for all disclosure of methods of using impedance measurement devices, as well as in Sections D and E of the present application.
  • the present invention is directed to a cell-substrate impedance measurement system
  • a cell-substrate impedance measurement system comprising a) at least one multiple-well cell-substrate impedance measuring device, in which at least two of the multiple wells comprise an electrode array at the bottom of the well and include a biological molecule or organic compound coating; b) an impedance analyzer electronically connected to the multiple-well cell-substrate impedance measuring device; c) a device station capable of engaging the one or more multiple- well devices and comprising electronic circuitry capable of selecting and connecting electrode arrays within any of the multiple wells to the impedance analyzer; and d) a software program connected to the device station and impedance analyzer to control the device station and perform data acquisition and data analysis from the impedance analyzer.
  • the impedance analyzer engages connection pads of one or more multi-well devices to measure impedance.
  • the impedance analyzer is capable of measuring impedance between 0.1 ohm and 10 5 ohm in frequency range of IHz to 1 MHz.
  • the impedance analyzer is preferably capable of measuring both resistance and reactance (capacitive reactance and inductive reactance) components of the impedance.
  • the impedance analyzer is capable of measuring impedance between 0.1 ohm and 10 3 ohm in frequency range of 100 Hz to 100 kHz.
  • a cell-substrate measurement system can be used to efficiently and simultaneously perform multiple assays by using circuitry of the device station to digitally switch from recording from measuring impedance over an array in one well to measuring impedance over an array in another well.
  • the system under software control is capable of completing an impedance measurement for an individual well at a single frequency within less than ten seconds.
  • the averaged time used by the system to complete an impedance measurement for an individual well at a single frequency is less than one second.
  • a multiple-well cell-substrate impedance measuring de ⁇ 'ice in a system of the present invention can be any multiple-well cell-substrate impedance measuring device in which at least two of the multiple wells comprise an electrode array at the bottom of the well, and in which at least two of the multiple wells comprise an electrode array are individually addressed.
  • the multi-well device takes the form of a specialized microtiler plate which has microelectronic sensor arrays integrated into the bottom of the wells and a biological molecule or organic compound covalently or noncovelently bound thereto.
  • a device used in a system of the present invention when connected to an impedance analyzer, can measure differences in impedance values that relate to cell behavior.
  • a cell-substrate impedance measuring device used in a system of the present invention can measure differences in impedance values when cells are attached to the electrode array and when cells are not attached to the electrode array, or can detect differences in impedance values when the number, type, activity, adhesiveness, or morphology of cells attached to the electrode-comprising surface of the apparatus changes.
  • the present invention can detect adhesion of cells as well as cell spreading.
  • Preferred devices that can be part of a cell-substrate impedance monitoring system can be those described in U.S. Patent Application No. 10/705,447, and in U.S. Patent Application No. 10/987,732, both herein incorporated by reference for disclosure of cell-substrate impedance monitoring devices that comprise electrode arrays, including disclosure of their design, composition, and manufacture.
  • Preferred devices that can be part of a cell-substrate impedance monitoring system can also be those described in the present application.
  • a multi-well device of a system of the present invention comprises between 4 and 1,536 wells, some or all of which can comprise electrode arrays.
  • a device station can comprise one or more platforms or one or more slots for positioning one or more multiwell devices.
  • the one or more platforms or one or more slots can comprise sockets, pins or other devices for electrically connecting the device to the device station.
  • the device station preferably can be positioned in a tissue culture incubator during cell impedance measurement assays. It can be electrically connected to an impedance analyzer and computer that are preferably located outside the tissue culture incubator.
  • the device station comprises electronic circuitry that can connect to an impedance monitoring device and an impedance analyzer and electronic switches that can switch on and off connections to each of the two or more electrode arrays of the rnultiwell devices used in the system.
  • the switches of the device station are controlled by a software program.
  • the software program directs the device station to connect arrays of the device to an impedance analyzer and monitor impedance from one or more of the electrode arrays.
  • the impedance analyzer can monitor impedance at one frequency or at more than one frequency.
  • impedance monitoring is performed at more than one time point for a given assay, and preferably, impedance is monitored at at least three time points.
  • the device station can connect individual arrays of a device to an impedance analyzer to monitor one, some, or all of the arrays of a device for a measurement time point.
  • the switches of the device station allow the selected individual arrays to be monitored in rapid succession for each desired monitoring time point.
  • Each monitoring time point is in fact a narrow time frame (for example from less than one second to minutes) of measurement in the assay during which impedance monitoring is performed.
  • the device station software is programmable to direct impedance monitoring of any of the wells of the device that comprise arrays at chosen time intervals.
  • the software of the impedance monitoring system can also store and display data. Data can be displayed on a screen, as printed data, or both. Preferably the software can allow entry and display of experimental parameters, such as descriptive information including cells types, compound concentrations, time intervals monitored, etc. Preferably, the software can also analyze impedance data. In preferred embodiments, the software can calculate a cell index (CI) for one or more time points for one or more wells of the multiwell device. In some preferred embodiments, the software can calculate a cell change index (CCI) from impedance measurements of one or more wells of the multiwell device. The software can preferably generate plots of impedance data and impedance values, such as but not limited to CI or CCI, with respect to time.
  • CI cell index
  • CCI cell change index
  • the software may perform other analysis as well, such as calculate cell number from CI, generate dose-response curves based on impedance data, calculate IC values based on impedance values, and calculate kinetic parameters of cell growth or behavior based on impedance values and impedance value curves.
  • the software of the impedance monitoring system can also store and display analyses of the data, such as calculated impedance values and kinetic parameters derived therefrom. Data can be displayed on a screen, as printed data, or both.
  • cell index in the present application is the same as "cell number index” in PCT Application No. PCT/US03/22557,entitled “IMPEDANCE BASED DEVICES AND METHODS FOR USE IN ASSAYS", filed on July 18, 2003 and in United States patent application No.
  • the present invention provides several methods of calculating cell index numbers for cells attached to two or more essentially identical arraj's of a cell-substrate impedance device, where the cells are monitored for impedance changes.
  • the methods calculate cell index number with better accuracy than previous methods of calculating cell index for cells on two or more arrays of a cell-
  • methods of calculating a cell index rely on novel methods for calculating the resistances of electrical traces leading to two or more essentially identical arrays.
  • the present invention therefore also includes methods of calculating resistances of electrical traces leading to two or more essentially identical arrays on a substrate.
  • two essentially identical electrode arrays will have electrode structures of the same dimensions (length, width, thickness), where the electrode structures have the same number of electrode elements, and the arrangement of electrode structures and electrode elements in each array are the same.
  • arrangement is meant the distance between structures or elements (gap width), their physical position with respect to one another, and their geometry (angles, degree of curvature, circle-on-line or castellated geometries, etc.), including the same features of any electrode buses that may be connected to electrode structures or electrode elements.
  • Electrodes of essentially identical arrays also comprise the same materials. For the purposes of calculating trace resistances and cell index number, a substrate can have any number of essentially identical arrays.
  • the following discussion provides novel methods of calculating cell index of cells adhered to arrays of a cell-substrate impedance monitoring device and novel methods for the calculation of the resistances of the electrical connection traces leading to two or more electrode arrays of a cell-substrate impedance monitoring device.
  • Impedance (Z) has two components, namely the resistance Rs and reactance Xs.
  • the impedance Z is expressed as follows,
  • serial resistance and serial reactance are equivalent.
  • Those who are skilled in electrical and electronic engineering can readily derive one form of expression from the parameter values in the other expression.
  • serial resistance and serial reactance are simply called resistance and reactance.
  • monitoring cell-substrate impedance for detection or measurement of change in impedance can be done by measuring impedance in any suitable range of frequencies.
  • the impedance can be measured in a frequency range from about 1 Hz to about 100 MHz.
  • the impedance can be.measured in a frequency range from about 100 Hz to about 2 MHz.
  • the impedance is typically a function of the frequency, i.e., the impedance values change as frequency changes.
  • Monitoring cell-substrate impedance can be done either in a single frequency or multiple frequencies. If the impedance measurement is performed at multiple frequencies, then a frequency-dependent impedance spectrum is obtained - i.e., there is an impedance value at each measured frequency.
  • the impedance has two components - a resistance component and a reactance component. A change in either resistance component or reactance component or both components can constitute a change in impedance.
  • the method for the measurement of electrical (or electronic) impedance is achieved by , (1) applying a voltage between or among said electrodes at a given frequency (or multiple frequencies, or having specific voltage waveform) and monitoring the electrical current through said electrodes at the frequency (or multiple frequencies, or having specific waveform), dividing the voltage amplitude value by the current amplitude value to derive the impedance value; (2) applying an electric current of a single frequency component (or multiple frequencies or having specific current wave form) through said electrodes and monitoring the voltage resulted between or among said electrodes at the frequency (or multiple frequencies, or having specific waveform), dividing the voltage amplitude value by the current amplitude value to derive the impedance value; (3) other methods that can measure or determine electric impedance.
  • the “division” is done for the values of current amplitude and voltage amplitude at same frequencies.
  • the current amplitude and voltage amplitude are expressed in the form of complex numbers, which take into account of how big the current and the voltage are and what the phase difference between the sinusoidal waves of the current and the voltage is.
  • the impedance value is also expressed in a complex form, having both resistance and reactance component, as shown in equations above.
  • the measured cell-substrate impedance can be used to calculate a parameter termed Cell Index or Cell Number Index.
  • Various methods for calculating such a cell number index can be used based on the changes in resistance or reactance when cells are attached to the electrode structures with respect to the cases no cells are attached to the electrode structures.
  • the impedance (resistance and reactance) of the electrode structures with no cell attached but with same cell culture medium over the electrode structures is sometimes referred as baseline impedance.
  • the baseline impedance ma) 7 be obtained by one or more of the following ways: (1) the impedance measured for the electrode structures with a cell-free culture medium introduced into the well containing the electrode structures, wherein the culture medium is the same as that used for the impedance measurements for the condition where the cell attachment or spreading is monitored; (2) the impedance measured shortly (e.g. 10 minutes) after the cell-containing medium was applied to the wells comprising the electrode structures on the well bottom (during the short period after cell-containing medium addition, cells do not have enough time to attach to the electrode surfaces.
  • the length of this short-period may depend on cell type and/or surface treatment or modification on the electrode surfaces); (3) the impedance measured for the electrode structures when all the cells in the well were killed by certain treatment (e.g. high- temperature treatment) and/or reagents (e.g. detergent) (for this method to be used, the treatment and/or reagents should not affect the dielectric property of the medium wl ⁇ ch is over the electrodes).
  • certain treatment e.g. high- temperature treatment
  • reagents e.g. detergent
  • the cell index or cell number index can be calculated by:
  • Cell Index is derived as
  • N is the number of the frequency points at which the impedance is measured. For example, if the frequencies used for the measurements are at 10 kHz. 25 kHz and 50 kHz. 50 kHz. is the resistance (cell-substrate resistance) of the electrode arrays or electrode structures when the cells are present on the electrodes at the frequency/ and is the baseline resistance of the electrode array or structures at the frequency/.
  • the cell index obtained for a given well reflects: 1) how many cells are attached to the electrode surfaces in this well, 2) how well cells are attached to the electrode surfaces in the well.
  • a higher value of "cell number index” indicates that, for same type of the cells and cells under similar physiological conditions, more cells are attached to the electrode surfaces.
  • Cell Index is a quantitative measure of cell number present in a well.
  • a higher value of "cell index” may also indicate that, for same type of the cells and same number of the cells, cells are attached better (for example, cells spread out more, or cell adhesion to the electrode surfaces is stronger) on the electrode surfaces.
  • the cell number index can be calculated by: (Bl) at each measured frequency, calculating the reactance ratio b ⁇ dividing the reactance of the electrode arrays when cells are present on and/or attached to the electrodes by the baseline reactance,
  • a zero or near-zero "cell number index” indicates that no cells or very small number of cells are present on or attached to the electrode surfaces.
  • a higher value of "cell number index'" indicates that, for same type of the cells and cells under similar physiological conditions, more cells are attached to the electrode surfaces.
  • the cell index can be calculated by: (Cl) at each measured frequency, subtracting the baseline resistance from the resistance of the electrode arrays when cells are present or attached to the electrodes to determine the change in the resistance with the cells present relative to the baseline resistance;
  • cell-number index is derived based on the maximum change in the resistance across the measured frequency range with the cells present relative to the baseline resistance. This cell index would have a dimension of ohm.
  • the cell index can be calculated by:
  • cell-number index is derived based on the maximum change in the magnitude of the impedance across the measured frequency range with the cells present relative to the baseline impedance. This cell index would have a dimension of ohm.
  • the index can be calculated by: (El) at each measured frequency, calculating the resistance ratio by dividing the resistance of electrode arrays when cells are present or attached to the electrodes by the baseline resistance,
  • cell-number index is derived based on multiple-frequency points, instead of single peak-frequency like above examples. Again, a zero or near-zero “cell number index” indicates that on cells are present on the electrodes. A higher value of “cell number index” indicates that, for same type of the cells and cells under similar physiological conditions, more cells are attached to the electrodes.
  • the cell index can be calculated by: (Fl) at each measured frequency, subtracting the baseline resistance from the resistance of the electrode arrays when cells are attached to the electrodes to determine the change in the resistance with the cells present relative to the baseline impedance; (here the change in the resistance is given by
  • M(J 1 ) R ⁇ 1 (J 1 ) - R ⁇ M for the frequency /, , R ⁇ 11 and ⁇ ,_ Wme are the serial resistances with the cells present on the electrode array and the baseline serial resistances, respectively); (F3) analyzing the frequenc) dependency of the change of the resistance to derive certain parameters that can quantify such dependency.
  • such parameters can be calculated a .
  • such parameter can be calculated as .
  • the parameter(s) are used as cell index or cell number index.
  • "'cell-number index” is derived based on the analysis of the frequency spectrum of the change in the resistance. Depending how the parameters are calculated, the cell index may have a dimension of ohm.
  • the cell index can be calculated by: (Gl) at each measured frequency, calculating the magnitude of the impedance
  • R,-cei ⁇ ⁇ d x ,-cau be ⁇ g & e serial resistance and reactance with the cells present on the electrode arrays, respectively, is the magnitude of the impedance of the electrode array with cells present on the electrode arrays, )
  • cell-number index' is derived based on the analysis of the frequency spectrum of the change in the magnitude of the impedance. Depending how the parameters are calculated, the cell index may have a dimension of ohm.
  • deriving "cell index” or “cell number index” and using such index to monitor cell conditions may have advantages. There are several advantages of using "cell number index” to monitor cell growth and/or attachment and/or viability conditions.
  • cell number index can also be used to compare different surface conditions. For the same electrode geometry and same number of cells, a surface treatment given a larger cell number index indicates a better attachment for the cells to the electrode surface and/or better surface for cell attachment.
  • the impedance of the electrode array (with or without cells present on the electrodes) is given by
  • Z mitC h is the impedance of electronic switch at its on stage
  • Ztrac e is the impedance of the electrical connection traces (or electrical conductive traces) on the substrate between the connection pads and the electrode buses
  • Z tota i is the total impedance measured at the impedance analyzer.
  • a method is invented in the present application to determine the impedance of electrical conductive (electrical connection) traces (mainly trace resistance, trace reactance is very small for the thin conductive firm trace) based on the relationships among two or more essentially identical arrays on a cell-substrate impedance monitoring device.
  • the four electrode arrays A. B C and D as indicated in Figure 1. are used to illustrate this method.
  • the electrical reactance (serial reactance) of the electronic switches and the electrical reactance (serial reactance) of the electrical connection traces are small as compared with_the corresponding electrical resistances (serial resistances).
  • the impedance determined from the impedance analyzer does contain both resistance (serial resistance. ) and reactance (serial reactance).
  • the measured total resistance , the resistance ) of electrical conductive (connection) trace, the switch resistance ) and the resistance of the electrode array satisfy the following equations:
  • N is the number of the segments of the trace- A and L A ., is the thickness, width and length of the i-th segment of the traces for the electrode array A, and p is the resistivity of the thin film.
  • the equation here applies to the film comprising a single type of metal.
  • the equation can be readily modified to be applicable to the film comprising two or more metal types (e.g. gold film over chromium adhesion layer).
  • the relationship among the trace resistances is simply determined by the pre-determined geometrical shapes (e.g. the length, width of the segments). For example, it would be straightforward to calculate the ratio a A _ D between the resistance of the electrically conductive traces for the electrode array A to the resistance of the electrically conductive traces for the electrode array D as below, where the film thickness is assumed to be the same everywhere on these traces and the resistivity is also the same everywhere on these traces,
  • Electrode-arrays A through D have essentially identical electrode structures, the electrode array resistances > should be of same, or very similar value for such a condition when all the electrode arrays are exposed to the same biological or chemical solutions or suspensions, i.e.: K- ⁇ my - D - If we assume the averaged electrode array resistance is , then these approximate relationship exists K-orr ⁇ >, ThUS, equations (1 OA - 1 OD) C an be changed to the following:
  • one aspect of the present invention is directed to a method of calculation of the resistances of the electrical connection traces s from the measured, total resistances fo ⁇ two or more essentially identical electrode arrays, comprising the following steps:
  • Another aspect of the present invention is directed to a method of calculating the resistance of the electrode arrays from the measured, total electrode resistances for two ro more essentially identical electrode arrays (such as, for example arrays A-D in Figure 1) if the same or similar solutions or suspensions are added to be in contact with the electrode assays, comprising the following steps:
  • the solutions or suspensions (for example, cell suspension) applied to each electrode array may have different compositions.
  • cell suspensions of different cell numbers may be used so that the suspensions applied to each electrode array are quite different.
  • the determination of the resistance of the electrode arrays with the cells present would require the determination of the resistance of the electrical connection traces by performing a "reference run” or "calibration run” in which the electrode arrays are exposed to a same, reference solution. From the "reference run", the resistances of the electrical connection traces can be determined.
  • the electrode arrays are exposed to the solutions or cell suspensions of interest and the resistances for the electrode arrays under such conditions are measured with an impedance analyzer or impedance measuring circuit.
  • the resistance of the electrode arrays with such cell suspensions present can be determined (or continuously determined) from the measured resistance by subtracting the sum of the resistance of the electronic switches and the resistance of the electrical connection traces for corresponding electrode arrays from the measured resistances.
  • another aspect of the present invention is directed to a method of calculating the resistance of the electrode arrays from the total electrical resistances measured at an impedance analyzer for essentially identical electrode arrays (such as electrode arrays A-D in Figure 1 used as an example) if different solutions or suspensions of interest are applied to the electrode assays, comprising the following steps: (1 ) exposing the electrode arrays to the solutions having same or similar solutions or suspensions (reference solutions):
  • the geometrical relationships between the electrode arrays are used to determine the factor a A _ D , a B _ D and a c _ D ;
  • step (1), (2) and (3) the steps of exposing the electrode arrays to reference solutions for the determination of the resistances of electrically conductive traces may be performed before or after the steps of applying the solutions or suspensions of interest to the electrode arra3's and measuring the total electrical resistance (step (4)).
  • step (4) may be performed first After that the solutions or suspensions of the interest may be removed from the electrode array.
  • the reference solutions can then be added to the electrode arrays (step (I)).
  • step (2) and step (3) can be then performed to determine the resistances of electrical connection traces.
  • Step (5) can be done.
  • step (1) and (2) can be performed ahead of step (4).
  • Another aspect of the present invention is directed to a method of determining the resistance of the electrode arrays with the cells present for a cell-based assay based on the total electrical resistance measured at an impedance analyzer for essentially identical electrode arrays.
  • the electrode arrays are exposed to a same, reference solution (for example, a same cell culture medium that does not contain any cells) and electrical measurement is conducted to determine the resistance of electrical connection traces.
  • electrical resistances of the electrical connection traces determined, electrical resistances of the electrode arrays with cell suspensions added to electrode arrays can be calculated from the total electrical resistances measured at an impedance analyzer.
  • Such total electrical resistance would include the resistance of the electrode arrays with cells present, the resistance of electronic switches and the resistance of electrical connection traces.
  • the method comprises following steps
  • the geometrical relationships between the electrode arrays are used to determine the factor a A _ D , a B _ D and a c _ D ;
  • step (1), (2) and (3) the steps of exposing the electrode arrays to reference solution for the determination of the electrical resistance of electrically conductive traces may be performed before or after the steps of applying the solutions of interest or cell suspensions of interest to the electrode arrays and measuring the total electrical resistance (step (4)).
  • step (4) may be performed first, followed by steps (1) and (2).
  • the cell suspensions of the interest may be removed from the electrode array.
  • reference solutions can be added to the electrode arrays.
  • step (5) is performed to determine the electrical resistance of electrode arrays with the cell suspensions of interest present.
  • the determination of the resistances of the electrical conductive traces for the electrode arrays that essentially identical electrode arrays may be, or may not be, part of the monitoring of cell- substrate impedance for cell-based assays. It depends on how the impedance data (measured at a single frequency or multiple frequencies, measured at multiple time points) of the electrode arrays is analyzed.
  • the resistances of the electrically conductive traces are needed, in order to remove the effect of the resistance of the electrically conductive traces on the analysis of the relative change of the resistance or impedance.
  • the Cell Index calculation method (F) described above there is no need to determine the resistances of the electrically conductive traces since the effect of the resistance of the electrically conductive traces is canceled out in the calculations.
  • the monitoring of the cell-substrate impedance may be or may not be based on the change with respect to the baseline impedance (or resistance).
  • a cell- based assay is performed to assess the effect of a test compound on the cells.
  • One method in performing such an assay is by monitoring of the cell-substrate impedance and determining the change in the cell-substrate impedance before and after the addition of the test compound to the cells.
  • the monitoring of cell-substrate impedance can be performed at a single frequency point or multiple frequency points, at a single time point or multiple time points after drug addition.
  • the impedance is first measured at a single frequency or multiple frequencies for the electrode arrays with the cells present just before addition of test compound.
  • the test compound is then added to the cells.
  • the impedance is then measured again at the same single frequency or multiple frequencies for the electrode arrays -with the cells after the addition of test compound.
  • Such post-compound addition measurement may be performed for many time points continuously in a regular or irregular time intervals.
  • the change in the cell-substrate impedances can be determined or quantified by subtracting the impedance(s) (resistance and/or reactance) measured before addition of the test compound from the impedance(s) (resistance and/or reactance) measured after addition of the test compound.
  • a single parameter or multiple parameters may be further derived for each time point after compound addition based on the calculated change in the cell-substrate impedances.
  • Such parameters are used to quantify the cell changes after compound addition.
  • Such approaches can be used further to analyze the responses of the cells to a test compound at multiple concentrations to derive dose-dependent response curves.
  • a "Normalized Cell Index" at a given time point is calculated by dividing the Cell Index at the time point by the Cell Index at a reference time point. Thus, the Normalized Cell Index is 1 at the reference time point.
  • Normalized cell index is cell index normalized against cell index at a particular time point. In most cases in the present applications, normalized cell index is derived as normalized relative to the time point immediately before a compound addition or treatment. Thus, normalized cell index at such time point (immediately before compound addition) is always unit one for all wells.
  • One possible benefit for using such normalized cell index is to remove the effect from difference in cell number in different wells. A well having more cells may produce a larger impedance response following compound treatment. Using normalized cell index, it helps to remove such variations caused by different cell numbers.
  • a "delta cell index" at a given time point is calculated by subtracting the cell index at a standard time point from the cell index at the given time point.
  • the delta cell index is the absolute change in the cell index from an initial time (the standard time point) to the measurement time.
  • the lime-dependent cellular response may be analyzed by d ⁇ ri ⁇ 'ing parameters that directly reflect the changes in cell status.
  • time dependent celluler response may be analyzed by calculating the slope of change in the measured impedance responses (that is equivalent to the first order derivative of the impedance response with respect to time, impedance response here can be measured impedance data or derived values such as cell index, normalized cell index or delta cell index).
  • the time-dependent cellular responses (including cytotoxicresposnes) responses may be analyzed for their higher order derivatives with respect to time. Such high order derivatives may provide additional information as for how cells responding to different compounds and as for the mechanisms of compound action.
  • Cell Change Index a parameter that can effectively link time dependent cell index I with cell status
  • CCI is the normalized rate of change in cell index.
  • CCI values can be used to quantify the cell status change.
  • the cell index determined by a cell-substrate impedance monitoring system described herein is expected to be a proportionate measure of the cell number in the well since the cell morphology and average extent of cell adhesion to the electrode surfaces among the whole cell population do not exhibit significant changes over time.
  • the cell index (CI) increase with time following an exponential function, such that
  • CJQ CI(O) * 2TM (6)
  • DT the cell doubling time.
  • CCI(t) is a constant si vino
  • CCI is about 0.7/DT
  • cell index increases in the same rate as that expected for an exponential growth of the cells.
  • CCI » 0.7/DT cell index increases faster than that expected for an exponential growth (or log growth) of the cells. This indicates that cells may grow faster than regular exponential growth, or cells may exhibit some morphology change (e.g. cell spreading out or adhering better to the electrode surfaces), leading to large impedance signal, or both of above effects, or there may be other cell behaviors occurring particular to the assay or culture conditions.
  • CCI CCI is more than zero but somewhat smaller than 0.7/DT
  • cell index increases in the rate slowed than that expected for an exponential growth. This indicates that cell growth rate may be slowed down relative to exponential growth, or cell growth may be somewhat inhibited by chemical compounds added to the culture media or by other cell culture parameters, or that certain populations of cells are dying off and detaching from the electrode surfaces, or there may be other cell behaviors occurring particular to the assay or culture conditions.
  • CCI is about zero, then cell index shows a near constant value. This may indicate that the cell growth is nearly-completely inhibited. For example, all the cells are arrested at certain points of cell cycle and are not progressing further. Or, this may indicate that the number of cells dying off in the culture is nearly as the number of newly-divided cells. .Alternatively this may indicate that cells reach stationary phase of cell culture. Alternatively this
  • ⁇ D may indicate that number of cells are above the detection upper limit of the cell-substrate impedance monitoring system. There is also the possibility of other cell behaviors occurring particular to the assay or culture conditions.
  • the present invention provide cell-based assays that can be performed in real time to assess cell proliferation, cell growth, cell death, cell morphology, cell membrane properties (for example, size, morphology, or composition of the cell membrane) cell adhesion, cell spreading and/or cell motility.
  • the assays can be cytotoxicity assays, proliferation assays, apoptosis assays, cell adhesion assays, cell activation or stimulation assays, anti-cancer compound efficacy assays, receptor-ligand binding or signal transduction analysis, assays of cytoskeletal changes, assays of cell structural changes (including but not limited to, changes in cell membrane size, morphology, or composition), cell quantification, cell quality control, time-dependent cytotoxicity profiling, assays of cell differentiation or de-differentiation, detection or quantitation of neutralizing antibodies, specific T-cell mediated cytotoxic effect assays, assays of cell adhesivity or spreading, assays of cell-cell interactions, analysis of microbial, viral, or environmental toxins, etc.
  • the assays are real-time assays in the sense that cell behavior or cell status being assayed can be assessed continuously at regular or irregular intervals.
  • Cell behaviors, cell responses, or cell status can be assayed and the results recorded or displayed within seconds to minutes of their occurrence.
  • the cell response during an assay can be monitored essential! ⁇ ' continuously over a selected time period. For example, a culture can be monitored every five to fifteen minutes for several hours to several days after addition of a reagent.
  • the interval between impedance monitoring, whether impedance monitoring is performed at regular or irregular intervals, and the duration of the impedance monitoring assay can be determined by the experimenter.
  • the cell-based impedance assays of the present invention avoid inadvertently biased or misleading evaluation of cell responses due to the time point or time points chosen for sampling or assaying the cells.
  • the assays do not require sampling of cell cultures or addition of reagents and thus eliminate the inconvenience, delay in obtaining results, and error introduced by many assays.
  • Patent Application No. 10/987,732 United States patent application numberl 0/705,615,entitled “Impedance based apparatuses and methods for analyzing cells and particles", filed on November 10, 2003, all incorporated herein by reference for their disclosure of cell-substrate impedance devices, systems, and methods of use. Additional details of cell-substrate impedance monitoring technology is further disclosed in the present invention.
  • cell-substrate impedance monitoring devices are used that have microelectrode arrays with appropriate geometries fabricated onto the bottom surfaces of wells such as microtiter plate wells, or have a similar design of having multiple fluid containers (such as wells) having electrodes fabricated on their bottom surfaces facing into the fluid containers.
  • Cells are introduced into the fluid containers of the devices, and make contact with and attach to the electrode surfaces. The presence, absence or change of properties of cells affects the electronic and ionic passage on the electrode sensor surfaces. Measuring the impedance between or among electrodes provides important information about biological status of cells present on the sensors.
  • analogue electronic readout signals can be measured automatically and in real time, and can be converted to digital signals for processing and for analysis.
  • cell-substrate impedance assays are performed using a system of the present invention that comprises a device of the present invention, an impedance monitor, a device station that comprises electronic circuitry and engages the device and the impedance analyzer, and a software program that controls the device station and records and analyzes impedance data.
  • a cell index can optionally be automatically derived and provided based on measured electrode impedance values.
  • the cell index obtained for a given well reflects: 1) how many cells are attached to the electrode surfaces in this well, and 2) how well (tightly or extensively) cells are attached to the electrode surfaces in this well.
  • the more the cells of same type in similar physiological conditions attach the electrode surfaces the larger the cell index.
  • the better the cells attach to the electrode surfaces e.g., the cells spread-out more to have larger contact areas, or the cells attach tighter to electrode surfaces, the larger the cell index.
  • a method for performing cell-based assays comprising: a) providing a cell-substrate impedance monitoring device of the present invention that comprises two or more electrode arrays, each of which is associated with a fluid container of the device and coated at least in part with a biological molecule or organic compound; b) attaching the device to an impedance monitor; c) introducing cells into one or more fluid containers of the device; and d) monitoring cell- substrate impedance of at least one of the fluid containers that comprises an electrode array and cells.
  • impedance is monitored from the at least one fluid container to obtain impedance measurements at at least three time points.
  • a method for performing cell-based assays in an impedance-monitoring system comprising: a) providing a cell- substrate impedance monitoring system of the present invention that comprises a device having two or more electrode arrays, each of which is associated with a well of the device and coated at least in part with a biological molecule or organic compound; b) introducing cells into one or more wells of the device; and c) monitoring cell-substrate impedance of at least one of the wells that comprises an electrode array and cells.
  • impedance is monitored from the one or more wells of the device to obtain impedance measurements at at least three time points.
  • impedance measurements or impedance values derived from impedance measurements from at least three time points are plotted versus time to generate one or more impedance curves for the one or more wells.
  • the method can be used to assay cell status, where cell status includes, but is not limited to, cell attachment or adhesion status (e.g. the degree of cell spread, the attachment area of a cell, the degree of tightness of cell attachment, cell morphology) on the substrate including on the electrodes, cell growth or proliferation status; number of viable cells and/or dead cells in the well; cytoskeleton change and re-organization and number of cells going through apoptosis and/or necrosis.
  • cell attachment or adhesion status e.g. the degree of cell spread, the attachment area of a cell, the degree of tightness of cell attachment, cell morphology
  • the cell-based assays that be performed with above methods include, but are not limited to, cell adhesion, cell apoptosis, cell differentiation, cell proliferation, cell survival, cytotoxicity, cell morphology detection, cell quantification, cell quality control, time-dependent cytotoxicity profiling, IgE-mediated cell activation or stimulation, receptor-ligand binding, viral and bacterial toxin mediated cell pathologic changes and cell death, detection and quantification of neutralizing antibodies, specific T-cell mediated cytotoxic effect, and cell-based assays for screening and measuring ligand-receptor binding.
  • cells are added to at least two fluid containers of a device, each of which comprises an electrode array, a biological molecule coating or organic compound coating, and impedance is monitored from at least two wells that comprise cells and an electrode array.
  • the cells used in the assay can be primary cells isolated from any species or cells of cell lines. Primary cells can be from blood or tissue. The cells can be engineered cells into which nucleic acids or proteins have been introduced. Ln some embodiments, different cell types are added to different wells and the behavior of the cell types is compared.
  • An impedance monitoring assay can be from minutes to days or even weeks in duration. Preferably, impedance is monitored at three or more time points, although this is not a requirement of the present invention. Impedance can be monitored at regular or irregular time intervals, or a combination of irregular and regular time intervals. In one embodiment of a cell-based impedance assay, the cell-substrate impedance is monitored at regular time intervals. In some embodiments of the present invention, impedance is monitored at irregular intervals and then at regular intervals during a particular time window of the assay. Impedance can be monitored at one frequency or at more than one frequency. For example, in some preferred embodiments, impedance is monitored over a range of frequencies for each time point at which impedance is monitored. Preferably, impedance is monitored at at least one frequency between about 1 Hz and about 100 MHz, more preferably at at least one frequency between about 100 Hz and about 2 MHz.
  • the present invention provides a method for performing real-time cell-based assay investigating the effect of a compound on cells, comprising: a) providing an above described system; b) seeding the cells to the wells of multiple-well devices; c) adding a compound to the wells containing cells; d) monitoring cell-substrate impedance before and after adding the compound at a regular or irregular time interval; wherein the time dependent impedance change provides information about time dependent cell status before addition of the compound and about time dependent cell status under the interaction of the compound.
  • Information about cell status includes, not limited to, cell attachment or adhesion status (e.g.
  • Information about cell status may also include any compound-cell interaction leading to any change to one or more of above cell status indicators. For example, if the compound binds to a receptor on the cell surface and such binding leads to a change in cell morphology, then the binding of compound to the receptor can be assayed by the monitored cell-substrate impedance.
  • the cell-based assays that be performed with above methods include, but not limited to, cell adhesion, cell apoptosis, cell differentiation, cell proliferation, cell survival, cytotoxicity, cell morphology detection, cell quantification, cell quality control, time-dependent cytotoxicity profiling, IgE-mediated cell activation or stimulation, receptor-ligand binding, viral and bacterial toxin mediated cell pathologic changes and cell death, detection and quantification of neutralizing antibodies, specific T-cell mediated cytotoxic effect, cell-based assay for screening and measuring ligand-receptor binding.
  • the cell-substrate impedance is monitored at regular time intervals.
  • the impedance is measured at a regular 2 hour, 1 hour, 30 min or 15 min time interval before and after adding the compound.
  • a real-time assay means that one can perform the measurement on cell-substrate impedance with various time resolutions, for example, measurement taking place at a longer time interval such as every hour or every two hours, or at a shorter time interval every minute or a few minutes.
  • Real-time assay does not mean that the measurements are provided in a continuous, uninterrupted fashion. In another word, real-time assay does not mean that the measurements are performed at every single moment.
  • the present invention provides methods for performing cell proliferation assays.
  • an increase in monitored impedance is indicative of an increases cell number.
  • the impedance measurements or impedance values derived from impedance measurements can be plotted versus time to obtain growth curves for cells growing in a fluid container of a cell-substrate monitoring device of the present invention.
  • the present invention provides a method of generating at least one cell growth curve, comprising: providing a device of the present invention having two or more electrode arrays, each of which is associated with a fluid container of the device; attaching the device to an impedance analyzer; adding cells to one or more fluid containers of the device; monitoring impedance from the one or more fluid containers to obtain impedance measurements at three or more time points after adding the cells to the one or fluid containers; and plotting the impedance measurements or values for the three or more time points versus time to generate at least one growth curve for the cells in the one or more fluid containers.
  • the present invention also provides a method of generating at least one growth curve using a system of the present invention, where the system includes a multi-well cell-substrate impedance monitoring device, an impedance analyzer, a device station, and a software program.
  • the method includes; providing a multi-well cell-substrate impedance measuring system; adding cells to one or more wells of the system; monitoring impedance from the one or more wells to obtain impedance measurements at three or more time points after adding cells to the one or more wells; and plotting impedance measurements or impedance values fo ⁇ the three or more time points versus time to generate a growth curve for the cells in the one or more wells.
  • impedance is monitored at four or more time points, in which at least one of the four or more time points is measured from a fluid container prior to adding cells to the fluid container.
  • impedance is monitored at regular or irregular time intervals for an assay period of from minutes to days.
  • proliferation assays can be performed by monitoring impedance for a period of between several hours and several days.
  • a plot can optionally be generated by plotting averaged impedance measurements of values at assayed time points for replicate wells versus time. Preferably, a standard deviation for the averaged values is also calculated.
  • a growth curve can be generated by plotting impedance measurements versus time, or by plotting cell index values that are calculated from impedance measurements, such as normalized cell index values or delta cell index values versus time.
  • the impedance measurement or cell index axis (typically the y-axis) can optionally use a log scale.
  • An impedance value can be any indices of impedance derived from impedance measurement, including, as nonlimiting examples, a cell index, a normalized cell index or a delta cell index.
  • impedance value can also be a "raw " measured or monitored impedance value.
  • Cell index (including normalized and delta cell index) can be a useful value for plotting growth curves, as it relates impedance measurements to cell number.
  • a delta cell index for a given time point can be derived by subtracting the cell index at a baseline point, such as a time point after cell attachment and just before log phase growth, from the cell index measurement at the given time point.
  • determinations of impedance values and generating growth curves based on impedance measurements or values can be performed by software, and preferably by software that interfaces directly with the impedance analyzer.
  • impedance values can be measured or derived or calculated and growth curves generated by a software program that controls and receives data from the impedance analyzer.
  • a growth curve generated from impedance measurements or cell index values can optionally be used to calculate one or more kinetic parameters of cell growth or behavior.
  • a growth curve can be used to calculate the length of a lag phase, cell attachment time, cell attachment rate, or a cell doubling time.
  • Two or more cell types can be seeded to separate wells in a proliferation assay using the methods of the present invention to generate growth curves of the two or more cell types.
  • the growth curves or kinetic parameters derived from the growth curves of the cell types can be compared.
  • the invention includes a method of generating growth curves for at least two cell types, comprising: providing a device of the present invention having two or more electrode arrays, each of which is associated with a fluid container of the device; attaching the device to an impedance analyzer; adding cells of two or more cell types to two or more fluid containers of the device, in which at least one of the two or more fluid containers receives one cell type and at least one other of the two or more fluid containers receives a different cell type, to provide two or more fluid containers comprising two or more different cell types; monitoring impedance from the two or more fluid containers comprising different cell types at three or more time points after adding the two or more cell types to the two or more fluid containers; and plotting impedance measurements or impedance values for the three or more time points versus time to generate a growth curve for the two or more cell types.
  • the present invention also provides a method of generating at least one growth curve using a system of the present invention, where the system includes a multi-well cell-substrate impedance monitoring device, an impedance analyzer, a device station, and a software program.
  • the method includes; providing a multi-well cell-substrate impedance measuring system; adding cells of two or more cell types to two or more wells of the device, in which at least one of the two or more wells receives one cell type and at least one other of the two or more wells receives a different cell type, to provide two or more wells comprising two or more different cell types; monitoring impedance from the two or more wells comprising different cell types at three or more time points after adding the two or more cell types to the two or more wells; and plotting impedance measurements or impedance values for the three or more time points versus time to generate a growth curve for the two or more cell types.
  • impedance is preferably monitored using an impedance monitoring device or system at four or more time points, in which at least one of the four or more time points is measured from fluid containers prior to adding cells to the fluid containers.
  • impedance is monitored at regular or irregular time intervals for an assay period of from minutes to days, for example, for a period of between several hours and several days.
  • a plot can optionally be generated by plotting averaged impedance measurements of values at assayed time points for replicate wells versus time. Preferably, a standard deviation for the averaged values is also calculated.
  • Impedance or impedance values such as cell index, normalized cell index, or delta cell index can be plotted versus time.
  • the impedance measurement or cell index axis (typically the y-axis) can optionally use a log scale.
  • a growth curve generated from impedance measurements or cell index values can optionally be used to calculate one or more kinetic parameters of cell growth or behavior. For example, a growth curve can be used to calculate the duration of a lag phase, cell attachment time, cell attachment rate, or a cell doubling time.
  • the growth curves of the two or more different cell types, or kinetic parameters derived from the growth curves of the two or more different cell types are compared to determine differences among the cell types in proliferation patterns or rates, or in kinetic parameters that can be derived from growth curves.
  • the different cell types used can be any cell types, incl ⁇ ding primary cells isolated from blood or tissue of an animal or human, or cells from cell lines.
  • proliferation rates of two types of primary cancer cell can be compared, or of primary cancer cells of the same type but different grades.
  • primary cells of individuals of different genotypes can be compared.
  • proliferation rates of primary or cell line stem cells can be compared.
  • growth curves or parameters of control and genetically modified cells of a cell line can be compared.
  • growth curves or parameters of cells infected with virus and control cells can be compared.
  • the present invention also includes a method of quantifying cells, comprising: providing a device of the present invention having two or more electrode arrays, each of which is associated with a fluid container of the device; attaching the device to an impedance analyzer; adding cells to one or more fluid containers of the device; monitoring impedance from the one or more fluid containers to obtain impedance measurements at one or more time points after adding the cells to the one or more fluid containers; deriving a cell index for the one or more time points; and using the cell index to determine the number of cells in the one or more fluid containers at least one of the one or more time points.
  • the cell index is used to determine the number of cells using a formula that relates cell index to cell number, in which the formula is obtained by: providing a device for cell-substrate monitoring, attaching the device to an impedance monitor: adding cells to one or more fluid containers of the device: measuring impedance of the one or more fluid containers comprising cells: calculating a cell index from the impedance measurements; determining the number of cells of said at least one fluid container at the time of impedance monitoring by a means other than impedance monitoring; and deriving a formula that relates the number of cells of the one or more fluid containers at the two or more time points with the impedance measurements at the two or more time points.
  • the number of cells introduced to the wells are pre-known or predetermined before cells are added in to the wells. Under such conditions, one assumes that there will be no change in cell number or little change in cell number when the impedance measurement for obtaining the formula is performed.
  • the number of cells determined by a method other than impedance monitoring can be determined by, for example, cell plating, hemacytometer counting, flow cytometry, or Coulter counting.
  • the method can also be practiced using an impedance monitoring system of the present invention, where the system includes a multi-well cell-substrate impedance monitoring device, an impedance analyzer, a device station, and a software program.
  • the method includes; providing a multi-well cell-substrate impedance measuring system; adding cells one or more wells of the system; monitoring impedance from the one or more wells comprising cells at one or more time points after adding the cells to the one or more wells; deriving a cell index for the one or more time points; and using the cell index to determine the number of cells in said at least well at at least one of said one or more time points.
  • the cell index is used to determine the number of cells using a formula that relates cell index to cell number, in which the formula is obtained by: providing a system for cell-substrate monitoring, where the system comprises at least one multi-well cell- substrate impedance monitoring device, adding cells to one or more wells of a device of the system; measuring impedance of the one or more wells comprising cells at two or more time points; calculating a cell index from the impedance measurement at the two or" more time points; determining the number of cells of the one or more wells at the two or more time points by a means other than impedance monitoring: and deriving a formula that relates the number of cells of the one or more wells at the two or more time points with the impedance measurements at the two or more time points.
  • the number of cells introduced to the wells are pre-known or predetermined before cells are added in to the wells. Under such conditions, one assumes that there will be no change in cell number or little change in cell number when the impedance measurement for obtaining the formula is performed.
  • the number of cells determined by a method other than impedance monitoring can be determined by, for example, cell plating, hemacytometer counting, flow cytometry, or Coulter counting.
  • Formulas relating cell index (including normalized cell index and delta cell index, which can also be used) to cell number for a given cell type can be used to quantitate cells of that type in assays using a cell-substrate impedance monitoring device, such as a device described herein.
  • a cell-substrate impedance monitoring device such as a device described herein.
  • the derived formulas relating cell index to cell number can be used in subsequent assays. There is no need to obtain the formula each time when an assay is performed. However, it is worthwhile to point that the formula can only be valid as long as the cells are under same physiological conditions in the assays where the formula was derived and where the formula is used.
  • the formula will not hold.
  • the formula may not hold.
  • Another point worth mentioning here is that relates the fact the derived cell index or impedance also depends on cell attachment quality on the surface as well as cell morphology. If cell morphology or cell attachment changes during an assay, then one need to distinguish between the changes caused by change in cell number or in cell morphology or in cell attachment.
  • the present invention provides a method for performing a cell-based assay investigating the effect of one or more test compounds on cells, comprising: providing a device of the present invention having two or more electrode arrays, each of which is associated with a fluid container or well that is at least in part coated with a biological compound or organic molecule; attaching the device to an impedance analyzer; introducing cells into two or more fluid containers of the device that comprise an electrode array; adding at least one test compound to at least one of the one or more of the fluid containers comprising cells and an electrode array to provide at least one test compound well; providing at least one control well to which cells are added that does not receive test compound; and monitoring cell-substrate impedance of the one or more test compound fluid containers and the one or more control fluid containers at least three time points after adding the one or more test compounds, and analyzing impedance measurements from the one or more test compound fluid containers and the one or more control fluid containers at at least three time points after adding the one or more test compounds, in which changes in impedance can provide information
  • the present invention also provides a method for performing a cell-based assay investigating the effect of one or more test compounds on cells, where the system includes a multi-well cell-substrate impedance monitoring device, an impedance analyzer, a device station comprising electronic circuitry that engages the device and connects the two or more electrode arrays of the device to the impedance analyzer, and a software program that controls the device station and can record and analyze data from the impedance analyzer.
  • the method includes: providing a multi-well cell-substrate impedance measuring system; introducing cells into two or more wells of the device coated with a biological molecule or organic compound; adding at least one test compound to at least one of the one or more of the wells comprising cells to pro ⁇ 'ide at least one test compound well; providing at least one control well to which cells are added that does not receive test compound; monitoring cell-substrate impedance of the one or more test compound wells and the one or more control wells at at least three time points after adding the one or more test compounds; and analyzing impedance measurements from the one or more test compound wells and the one or more control wells at at least three time points after adding the one or more test compounds, in which changes in impedance can provide information about cell responses to the one or more test compounds.
  • a test compound can be any compound, including a small molecule, a large molecule, a molecular complex, an organic molecule, an inorganic molecule, a biomolecule such as but not limited to a lipid, a steroid, a carbohydrate, a fatty acid, an amino acid, a peptide, a protein, a nucleic acid, or any combination of these.
  • a test compound can be a synthetic compound, a naturally occurring compound, a derivative of a naturally-occurring compound, etc. The structure of a test compound can be known or unknown.
  • Information about cell responses to the one or more test compounds includes, but is not limited to, information about cell attachment or adhesion status (e.g. the degree of cell spread, the attachment area of a cell, the degree of tightness of cell attachment, cell morphology) on the substrate including on the electrodes, cell growth or proliferation status; number of viable cells and/or dead cells in the well; cytoskeleton change and re ⁇ organization and number of cells going through apoptosis and/or necrosis.
  • Information about cell status may also include any compound-cell interaction leading to any change to one or more of above cell status indicators. For example, if the compound binds to a receptor on the cell surface and such binding leads to a change in cell morphology, then the binding of compound to the receptor can be assayed by the monitored cell-substrate impedance.
  • the cells used in the assay can be primary cells isolated from any species or can be cells of cell lines.
  • the cells can be genetically engineered cells (For example, cells from a genetically modified organism, such as for example from a '"gene knockout"' organism, or cells that have been engineered to over-express an endogenous gene or a transgene. or cells whose normal gene expression has been manipulated by use of antisense molecules or silencing RNA.)
  • different cell types are added to different wells and the behavior of the different cell types in response to one or more compounds is compared.
  • the cell-based assays that be performed with above methods include, but are not limited to, cell adhesion, cell spreading apoptosis, cell differentiation, cell proliferation, cell survival, cytotoxicity, cell morphology detection, cell quantification, cell quality control, time-dependent cytotoxicity profiling, IgE-mediated cell activation or stimulation, receptor-ligand binding, viral, bacterial, or environmental toxin mediated cell pathologic changes or cell death, detection or quantification of neutralizing antibodies, specific T-cell mediated cytotoxic effect, and cell-based assay for screening or measuring ligand-receptor binding.
  • impedance is preferably monitored from at least one test compound well at at least one time point before adding said at least one test compound to said at least one test compound well.
  • impedance is monitored at four or more time points, at least one of which is prior to the addition of one or more test compounds.
  • impedance is monitored at regular or irregular time intervals for an assay period of from minutes to days, for example, for a period of between several hours and several days.
  • the cell-substrate impedance is monitored at at least one time point prior to addition of the test compound, and at regular time intervals thereafter.
  • impedance can be measured at one or more intervals before adding the compound and at a regular 2 hour, 1 hour, 30 min or 15 min time intervals after adding the compound.
  • impedance is measured at three or more time points spaced at regular intervals.
  • a real-time assay means allows one to perform the measurement on cell-substrate impedance with various time resolutions, for example, measurement taking place at a longer time interval such as every hour or every two hours, or at a shorter time interval every minute or a few minutes.
  • Impedance can be monitored at one frequency or at more than one frequency.
  • impedance is monitored over a range of frequencies for each time point at which impedance is monitored.
  • impedance is monitored at at least one frequency between about 1 Hz and about 100 MHz. More preferably at at least one frequency between about 100 Hz and about 2 IvIHz.
  • impedance measurements or values can be averaged for the assayed time points for replicate wells.
  • a standard deviation for the averaged values is also calculated.
  • analyzing impedance can comprise plotting cell impedance versus time to obtain at least one test compound impedance curve and at least one control impedance curve.
  • at least one test compound impedance curve and said at least one control impedance curve are compared to identify a time frame, if any, in which a test compound curve differs significantly from a control curve, indicating a time frame of an effect of a test compound on cells.
  • the test compound can be hypothesized to affect one or more of, for example, cell attachment or adhesion, cell growth or proliferation, cytoskeleton organization or function, or apoptosis or cell death.
  • data from impedance monitoring of a well that comprises cells and a test compound is compared with data from impedance monitoring of a well that comprises cells in the absence of a test compound, however, this is not a requirement of the present invention.
  • cell number index Methods of calculating a cell index (cell number index) are disclosed herein as well as in parent application U.S. Patent Application 10/705,447, U.S. Patent Application No. 10/987 ; 732.both herein incorporated by reference for disclosures relating to cell number index and its calculation.
  • the cell index calculated from impedance measurements of wells receiving compound can be compared with the cell index calculated from k ⁇ p ⁇ dance measurements of control wells to assess the effect of a compound on cells.
  • cell index calculated from impedance measurements of wells from one or more time points after the addition of a compound can be compared with the cell index calculated from impedance measurements of wells from one or more time points prior to the addition of a compound to assess the effect of a compound on cells.
  • the cell index can be used as an indicator of cytotoxicity.
  • Cell index values (including normalized cell index values and delta cell index values) from at least three time points from at least one test compound well and at least one control well can be plotted versus tune to obtain one or more test compound cell index curve and one or more control cell index curves.
  • the one or more test compound cell index curves and the one or more control cell index curves can be compared to identify a time frame, if any, in which a test compound curve differs significantly from a control curve, indicating a time frame of an effect of a test compound on cells.
  • the test compound can be hypothesized to affect one or more of, for example, cell attachment or adhesion, cell growth or proliferation, cytoskeleton organization or function, or apoptosis or cell death.
  • Cell index values at three or more assay time points for one or more test compound wells and one or more control wells can be used to derive cell change index (CCI) values or a second order derivatives of cell index at three or more assay time points.
  • CCI cell change index
  • the value of CCI at a give time point can be determined to be either approximately equal to 0.7, much greater than 0.7, greater than zero and less than 0.7, approximately equal to zero, less than zero, or much less than zero. These values can indicate cell behavior at an assay time point, as CCI approximately equal to 0.7 indicates log rate growth, a CCI much greater than 0.7 indicates faster than log rate growth, a CCI greater than zero and less than 0.7 indicates slower than log rate growth, a CCI approximately equal to zero indicates no growth (a constant cell index), a CCI less than zero indicates cells are detaching from the substrate, and a CCl much less than zero indicates cell are detaching rapidly from the substrate. For a given assay time point, differences in CCI value between control and compound treated w ells can indicate a time at which the compound has an effect on cells, as well as providing information on the type of effect the compound has.
  • the CCI can further be used to obtain information on the effect of a test compound by plotting CCI versus time for at least three assay time points to obtain a cell change index curve (CCI curve) for at least one control container or well and at at least one test compound container or well.
  • CCI curve cell change index curve
  • One or more test compound CCI curves can be compared with one or more control CCI curves to obtain information on cell status or behavior in response to said at least one test compound, wherein said cellular status or behavior is at least one of: cell attachment or adhesion status; cell growth or proliferation status; the number of viable cells or dead cells; cytoskeleton change or re-organization; or the number of cells going through apoptosis or necrosis.
  • the present invention also provides methods of comparing the effects of a compound on two or more cell types.
  • the method comprises: providing a device of the present invention having two or more electrode arrays, each of which is associated with a fluid container of the device; attaching the device to an impedance analyzer; introducing cells into two or more fluid containers of the device that comprise an electrode array, wherein at least one of the two or more fluid containers receives one cell type and at least one other of the two or more fluid containers receives a different cell type; adding a test compound to the one or more fluid containers receiving one cell type and adding the test compound to the one or more fluid containers receiving a different cell type to provide at least two test compound fluid containers that comprise cells of different types; providing at least two control fluid containers that do not receive test compound, in which at least one of the control fluid containers receives cells of the one type and at least one of the control fluid containers receives cells of the different type; monitoring cell-substrate impedance of the two or more test compound fluid
  • the present invention also provides a method for performing a cell-based assay investigating the effect of one or more test compounds on cells using a cell-substrate impedance monitoring system of the present invention, where the system includes a multi-well cell-substrate impedance monitoring device, an impedance analyzer, a device station comprising electronic circuitry that engages the device and connects the two or more electrode arrays of the device to the impedance analyzer, and a software program that controls the device station and can record and analyze data from the impedance analyzer.
  • the method includes: providing a multi-well cell-substrate impedance measuring system; introducing cells into two or more wells of the device that comprise an electrode array, wherein at least one of the two or more wells receives one cell type and at least one other of the two or more wells receives a different cell type; adding a test compound to the one or more wells receiving one cell type and adding the test compound to the one or more wells receiving a different cell type to provide at least two test compound wells that comprise cells of different types; providing at least two control wells that do not receive test compound, in which at least one of the wells receives cells of the one type and at least one of the control wells receives cells of the different type; monitoring cell-substrate impedance of the two or more test compound wells that comprise different cell types and the one or more control wells at at least three time points after adding the one or more test compounds; and analyzing impedance measurements from the two or more test compound wells comprising different cell types and from the one or more control wells at at least
  • impedance is preferably monitored from at least two test compound wells comprising different cell types at at least one time point before adding test compound to the at least one two compound wells.
  • impedance is monitored at four or more time points, af least one of which is prior to the addition of one or more test compounds.
  • impedance is monitored at regular or irregular time intervals for an assay period of from minutes to days, for example, for a period of between several hours and several days.
  • the cell-substrate impedance is monitored at at least one time point prior to addition of the test compound, and at regular time intervals thereafter.
  • impedance can be measured at one or more intervals before adding the compound and at a regular 2 hour, 1 hour, 30 min or 15 min time intervals after adding the compound.
  • impedance is measured at three or more time points spaced at regular intervals.
  • a real- time assay means allows one to perform the measurement on cell-substrate impedance with various time resolutions, for example, measurement taking place at a longer time interval such as every hour or every two hours, or at a shorter time interval every minute or a few minutes.
  • Impedance can be monitored at one frequency or at more than one frequency. For example, in some preferred embodiments, impedance is monitored over a range of frequencies for each time point at which impedance is monitored. Preferably, impedance is monitored at at least one frequency between about 1 Hz and about 100 MHz, more preferably at at least one frequency between about 100 Hz and- about 2 MHz.
  • a test compound can be any compound whose effect on cells can be investigated.
  • a test compound used in assays comparing cell responses can be a compound whose effect on one or more of the cell types to be assayed is known, or can be a compound whose effects on any of the cell types to be assayed are unknown.
  • cells are introduced into at least three wells of the device that each comprise an electrode array, and at least one well that comprises an electrode array and comprises cells does not receive a test compound.
  • a control well that does not receive a test compound can be monitored, and its impedance data can be compared with that of wells that receive a compound to determine the effect of the test compounds on cells.
  • the cell types used in the assay can be primary cells isolated from any species or can be cells of cell lines.
  • the different cell types are the same type of cell from different individuals, and thus have different genotypes.
  • One or more of the cell types can be genetically engineered (For example, cells from a genetically modified organism, such as for example from a "gene knockout " organism, or cells that have been engineered to overexpress an endogenous gene or a transgene, or cells whose normal gene expression has been manipulated by use of antisense molecules or silencing RNA.) In these cases, genetically modified cells can be compared with control cells.
  • the cells can be, for example, stem cells from different stages of differentiation or of different genotypes whose response to growth factors is being compared.
  • the cells can be cancer cells where the test compound is tested for its cytotoxic effects.
  • the cells can be primary cancer cells of the same type isolated from different individuals, for example, or different cancer cell lines, or cancer cells of the same type but of different grades.
  • three or more different cell types are added to different wells and the behavior of the three or more different cell types in response to one or more compounds is compared.
  • assays can be employed, where the effect of a test compound on the behavior of two or more cell types in the assay is under investigation.
  • assays include, as nonlimiting examples, cell adhesion assays, apoptosis assays, cell differentiation assays, cell proliferation assays, cell survival assays, cytotoxicity assays, cell morphology detection assays, cell quantification assays, cell quality control assays, time-dependent cytotoxicity profiling assays, IgE-mediated cell activation or stimulation assays, receptor-ligand binding assays, viral, bacterial, or environmental toxin mediated cell pathologic changes or cell death assays, detection or quantification of neutralizing antibodies, specific T-cell mediated cytotoxic effect assays, and cell-based assays for screening or measuring ligand-receptor binding.
  • the assays of the present invention is preferable to perform replicate test compound assays in which more than one fluid container of cells of the same type receives the same compound at the same concentration.
  • impedance measurements or values can optionally be averaged for the assayed time points for replicate wells.
  • a standard deviation for the averaged values is also calculated.
  • time-d ⁇ pendent responses of the first and second types of cells are compared to see how similar or different the responses from the two types of cells are.
  • impedance from a first cell type well is plotted versus time to give a first cell type impedance curve and impedance from a second cell type well is plotted versus time to give a second cell type impedance curve.
  • Cell index (including normalized cell index or delta cell index) from wells comprising cells of different types can also be calculated from impedance data and plotted versus time to give cell index curves.
  • the impedance curves or cell index curves from the different cell types can be compared to determine whether the time frame, magnitude, and duration of a cells response to a compound are similar or different.
  • impedance curves or cell index curves generated from control wells comprising each cell type in the absence of compound are compared with the test compound curves to assess the compound-specific effects on each cell type.
  • the effects of the compounds on one or more of the two or more cell types can be effects on cell attachment or adhesion, cell growth or proliferation; the number of viable cells or dead cells; cytoskeleton organization or function; or the number of cells going through apoptosis or necrosis in response to a test compound.
  • Assays can be designed to investigate the compound's effects on particular cellular processes or activities.
  • the effect of a compound on at least one of the cell types used in the assay may be known.
  • the mechanism of action of a compound on at least one of the cell types used in the assay may be known.
  • comparison of the compound response of one or more different cell types with the compound response of a cell type whose response to the compound is characterized can give information as to the similarity or difference in response of a different cell type to the compound.
  • the CI derived from impedance data from wells comprising different cell types and a test compound can be used to derive cell change index (CCI) values for assay time points.
  • CCI values of particular cell types at assay time points can be compared. Such comparisons can indicate whether different cell types are responding similarly to a compound.
  • CCI can also be plotted versus time, and CCI curves of cells of different types assayed with one or more test compounds can be compared to determine the similarities or differences in cellular responses of different cell types to a test compound.
  • the present invention also provides methods of comparing the effects of two or more different compounds on cells.
  • the method comprises: providing a device of the present invention having three or more electrode arrays, each of which is associated with a fluid container of the device; attaching the device to an impedance analyzer; introducing cells into three or more fluid containers of the device that comprise an electrode array; adding at least one test compound to at least one of the three or more fluid containers comprising cells and adding at least one different test compound to at least one other of the three or more fluid containers comprising cells to provide at least two different test compound fluid containers; providing as a control fluid container at least one of the three or more fluid containers, in which the control fluid container receives cells but does not receive compound; attaching an impedance analyzer to the device; monitoring cell-substrate impedance of the two or more different test compound fluid containers that comprise different compounds and the one or more control fluid containers at at least three time points after adding the one or more test compounds; and analyzing impedance measurements from the
  • the present invention provides a method for performing a cell- based assay investigating the effect of two or more test compounds on cells using a cell- substrate impedance monitoring system.
  • the method includes: a) providing a cell- substrate impedance monitoring system of the present invention; b) introducing cells into at least two wells of the device that each comprise an electrode array; c) adding to at least one well of the device comprising cells and an electrode array a first test compound: d) adding to at least one other well of the device comprising cells and an electrode array a second test compound; and e) monitoring cell-substrate impedance of at least one well comprising cells and a first compound and at least one well comprising cells and a second compound, in which changes in impedance can provide information about cell responses to the first and second compounds.
  • time-dependent responses of cells to the first compound and the second compound are compared to see how similar or different the responses from the two compounds are.
  • time-dependent cytotoxic responses are compared.
  • the cells and test compound that can be used in the assay can be any as described above for assays testing effects of test compounds.
  • the assays of the present invention is preferable to perform replicate test compound assays in which more than one fluid container of cells of the same type receives the same compound at the same concentration.
  • impedance measurements or values can optionally be averaged for the assayed time points for replicate wells.
  • a standard deviation for the averaged values is also calculated.
  • Impedance monitoring can be as described above for assays testing effects of test compounds.
  • impedance is monitored from the at least two different test compound wells and at least one control well at at least one time point before adding said at least one test compound to said at least one test compound well.
  • impedance is monitored at four or more time points, at least one of which is prior to the addition of one or more test compounds.
  • impedance is monitored at regular or irregular time intervals for an assay period of from minutes to days, for example, for a period of between several hours and several days.
  • the cell-substrate impedance is monitored at at least one time point prior to addition of the test compound, and at regular time intervals thereafter.
  • impedance can be measured at one or more intervals before adding the compound and at a regular 2 hour, 1 hour, 30 min or 15 min time intervals after adding the compound.
  • impedance is measured at three or more time points spaced at regular intervals.
  • a real-time assay means allows one to perform the measurement on cell-substrate impedance with various time resolutions, for example, measurement taking place at a longer time interval such as every hour or ever ⁇ ' two hours, or at a shorter rime interval every minute or a few minutes.
  • Impedance can be monitored at one frequency or at more than one frequency.
  • impedance is monitored over a range of frequencies for each time point at which impedance is monitored.
  • impedance is monitored at at least one frequency between about 1 Hz and about 100 MHz. More preferably at at least one frequency between about 100 Hz and about 2 MHz.
  • data from impedance monitoring of wells that comprise different test compounds are compared.
  • impedance at three or more assay time points can be plotted versus time.
  • impedance at the same three or more assay time points is also plotted versus time.
  • the impedance curves of different compound wells can be compared with the control impedance curve to determine whether the compounds have a similar or different effect on cells.
  • Cell index (including normalized cell index or delta cell index) from wells comprising cells of different types can also be calculated from impedance data and plotted versus time to give cell index curves.
  • the impedance curves or cell index curves from the different cell types can be compared to determine whether the time frame, magnitude, and duration the response of cells to different compounds are similar or different.
  • impedance curves or cell index curves generated from one or more control wells comprising cells in the absence of compound are compared with the test compound curves to assess the compound-specific effects of each compound.
  • the effects of the compounds on cells can be for example, effects on cell attachment or adhesion, cell growth or proliferation; the number of viable cells or dead cells; cytoskeleton organization or function; or the number of cells going through apoptosis or necrosis in response to a test compound.
  • Assays can be designed to investigate the compound's effects on particular cellular processes or activities.
  • the effect on cells of one or more of the compounds used in the assay may be known.
  • the mechanism of action of one or more compounds used in the assay may be known. In such cases, comparison of the responses of cells to other test compounds used in the assay with cellular responses to the one or more compounds whose effects are characterized can give information as to the similarity or difference in response of different compounds to a known compound.
  • Information about cell responses to the compound includes, but is not limited to, information about cell attachment or adhesion status (e.g. the degree of cell spread, the attachment area of a cell, the degree of tightness of cell attachment, cell morphology) on the substrate including on the electrodes, cell growth or proliferation status; number of viable cells and/or dead cells in the well; cytoskeleton change and re-organization and number of cells going through apoptosis and/or necrosis.
  • Information about cell status may also include any compound-cell interaction leading to any change to one or more of above cell status indicators.
  • the binding of compound to the receptor can be assayed by the monitored cell-substrate impedance.
  • the cell-based assays mat be performed with above methods include, but not limited to, cell adhesion, cell apoptosis, cell differentiation, cell proliferation, cell survival, cytotoxicity, cell morphology detection, cell quantification, cell quality control, time-dependent cytotoxicity profiling, IgE-mediated cell activation or stimulation, receptor-ligand binding, viral and bacterial toxin mediated cell pathologic changes and cell death, detection and quantification of neutralizing antibodies, specific T-cell mediated cytotoxic effect, cell-based assay for screening and measuring ligand-receptor binding.
  • a plurality of compounds can be assayed with multiple cell types. In one preferred embodiment of this method, time-dependent cytotoxic responses of different cell types to a set of compounds are compared.
  • the CI derived from impedance data from wells comprising different cell types and a test compound can be used to derive cell change index (CCI) values for assay time points.
  • CCI values of particular cell types at assay time points can be compared. Such comparisons can indicate whether different cell types are responding similarly to a compound.
  • CCI can also be plotted versus time, and CCI curves of cells of different types assayed with one or more test compounds can be compared to determine the similarities or differences in cellular responses of different cell types to a test compound. For example, the time frame, magnitude, and duration of a difference in response as evidenced by the curves can indicate a difference in efficacy or mechanism of compounds.
  • the impedance differences can reflect differences in.
  • cell attachment or adhesion cell growth or proliferation: the number of viable cells or dead cells: cytoskeleton organization or function; or the number of cells going through apoptosis or necrosis in response to a test compound.
  • assays can be employed, where the effect of two or more test compound on the behavior cells is under investigation.
  • Such assays include, as nonlimiting examples, cell adhesion assays, apoptosis assays, cell differentiation assays, cell proliferation assays, cell survival assays, cytotoxicity assays, cell morphology detection assays, cell quantification assays, cell quality control assays, time-dependent cytotoxicity profiling assays, IgE-mediated cell activation or stimulation assays, receptor- Hgand binding assays, viral, bacterial, or environmental toxin mediated cell pathologic changes or cell death assays, detection or quantification of neutralizing antibodies, specific T-cell mediated cytotoxic effect assays, and cell-based assays for screening or measuring ligand-receptor binding.
  • Cytotoxicity profiling in which the impedance responses of cells in response to a plurality of potentially cytotoxic compounds are compared, can provide information on the efficacy and mechanism of a test compound. Cytotoxicity profiling can be performed by comparing any combination of impedance plots, kinetic parameters derived from impedance plots, CI plots, CCI values, and CCI plots.
  • analyzing the cytotoxicity response may include derivation of the slope of change in the time dependent cytotoxicity response at a given compound concentration.
  • analyzing real-time cytotoxicity response may include derivation of high-order derivatives of the time dependent cytotoxicity response with respect to time at a given compound concentration.
  • a method for testing different concentrations of a test compound on cells comprises: providing a device of the present invention having three or more electrode arrays, each of which is associated with a fluid container of the device; attaching the device to an impedance analyzer: introducing cells into at least two of the three or more fluid containers of the device that comprise an electrode array; adding different concentrations of a test compound to the two or more fluid containers of the device that comprise cells; providing a control fluid container that comprises cells but does not receive compound; monitoring cell-substrate impedance of the two or more different test compound fluid containers that comprise different concentrations of a test compound and of the one or more control fluid containers at at least three time points after adding a test compound; and analyzing impedance measurements from the two or more different test compound fluid containers and one or more control fluid containers at at least three time points after adding a test compound
  • the present invention provides a method for performing a cell- based assay investigating the effect of two or more concentrations of a test compound on cells using a cell-substrate impedance monitoring system.
  • the method includes: providing a cell- substrate impedance monitoring system of the present invention; introducing cells into at least two of the three or more wells of the device that comprise an electrode array; adding different concentrations of a test compound to the two or more wells of the device that comprise cells; providing a control well that comprises cells but does not receive test compound; monitoring cell-substrate impedance of the two or more different test compound wells mat comprise different concentrations of a test compound and the one or more control wells at at least three time points after adding a test compound; and analyzing impedance measurements from the two or more different test compound wells and the one or more control wells at at least three time points after adding a test compound, in which changes in impedance can provide information about cell responses to the test compounds.
  • the cells and test compound that can be used in the assay can be any as described above for assays testing effects of test compounds.
  • Impedance monitoring can be as described above for assays testing effects of test compounds.
  • impedance is monitored from the at least two different test compound wells and at least one control well at at least one time point before adding said at least one test compound to said at least one test compound well.
  • impedance is monitored at four or more time points, at least one of which is prior to the addition of one or more test compounds.
  • impedance is monitored at regular or irregular time intervals for an assay period of from minutes to days, for example, for a period of between several hours and several days.
  • the cell -substrate impedance is monitored at at least one time point prior to addition of the test compound, and at regular time intervals thereafter.
  • impedance can be measured at one or more intervals before adding the compound and at a regular 2 hour, 1 hour, 30 min or 15 min time intervals after adding the compound.
  • impedance is measured at three or more time points spaced at regular intervals.
  • a real-time assay means allows one to perform the measurement on cell-substrate impedance with various time resolutions, for example, measurements taking place at a longer time interval such as every hour or every two hours, or at a shorter time interval every minute or a few minutes.
  • Impedance can be monitored at one frequency or at more than one frequency. For example, in some preferred embodiments, impedance is monitored over a range of frequencies for each time point at which impedance is monitored. Preferably, impedance is monitored at at least one frequency between about 1 Hz and about 100 MHz, more preferably at at least one frequency between about 100 Hz and about 2 MHz.
  • impedance or, preferably, cell index (including normalized cell index or delta cell index)
  • cell index including normalized cell index or delta cell index
  • impedance at the same three or more assay time points is also plotted versus time.
  • An impedance curve or cell index curve can give an indication of the time frame at which a compound affects cell response.
  • the cell index can be used as an indicator of cytotoxicity. Cytotoxicity Profiling
  • the present invention provides a method for performing real-time c)i;otoxi city assay of a compound, comprising: a) providing an above described system; b) seeding cells to the wells of multiple-well devices; c) adding the compound to the wells containing cells; d) monitoring cell-substrate impedance before and after adding the compound at a regular or irregular time interval; wherein the time dependent impedance change provides information about time dependent cytotoxicity of the compound.
  • the cell-substrate impedance is monitored at regular time intervals.
  • the impedance is measured at a regular 2 hour, 1 hour, 30 min or 15 min time interval before and after adding the compound.
  • the present invention provides a method for analyzing and comparing time-dependent cytotoxic effects of a first compound and a second compound on a cell type, comprising : a) performing a real-time cytotoxicity assay on a cell type with the first compound using the method described above; b) performing a real-time cytotoxicity assay on said cell type with the second compound using the method described above; c) comparing the time-dependent cytotoxic responses of the first compound and the second compound to see how similar or different the responses from the two compounds are.
  • time-dependent cytotoxic responses are determined for the first compound at multiple dose concentrations. In another embodiment, time-dependent cytotoxic responses are determined for the second compound at multiple dose concentrations. In yet another embodiment, time-dependent cytotoxic responses are determined for both first compound and second compound at multiple dose concentrations.
  • the first compound is a compound with a known mechanism for its cytotoxic effect and the second compound is a compound with an unknown mechanism for its cytotoxic effect. If the time dependent cytotoxic responses from the second compound are similar to that of the first one, the second compound may follow a similar mechanism for its cytotoxic effect to the first compound. ⁇ 'arious approaches may be used in comparing the cytotoxic responses of the compounds. A cell index (or cell number index) can optionally be calculated using the impedance values obtained. In one embodiment of the method described above, time dependent IC50 ma ⁇ ' be derived for the compounds and comparison between their cytotoxic responses is done by comparing their time dependent IC50 curves based on cell index values.
  • the two compounds may follow a similar mechanism for inducing cytotoxicty effects.
  • direct comparison of time-dependent cytotoxic responses of two compounds are done where the concentrations for the two compounds may be the same or may be different. Direct comparison between time-dependent cytotoxic responses may be done by analyzing the slope of change in the measured responses (that is equivalent to the first order derivative of the response with respect to time) and comparing the time-dependent slopes for the two compounds. In another approach, the time-dependent cytotoxic responses may be analyzed for their higher order derivatives with respect to time. Comparing such high order derivatives may provide additional information as for the mechanisms of compound-induced cytotoxicity.
  • analyzing real-time cytotoxicity response may include the derivation of time-dependent IC50 values for the compound on the multiple cell types.
  • analyzing real-time cytotoxicity response may include derivation of the slope of change in the time dependent cytotoxicity response at a given compound concentration.
  • analyzing real-time cytotoxicity response may include derivation of high-order derivatives of the time dependent cytotoxicity response with respect to time at a given compound concentration.
  • the above methods are applied to perform cytotoxicity profiling of multiple compounds on multiple cell types.
  • analyzing real-time cytotoxicity response may include derivation of the slope of change in the time dependent cytotoxicity response at a given compound concentration. In yet another embodiment of the method, analyzing real-time cytotoxicity response may include derivation of high-order derivatives of the time dependent cytotoxicity response with respect to time at a gi ⁇ 'en compound concentration.
  • cell index is calculated using the same method as the Cell Index calculation method (A) as described in Section C of the present application.
  • Normalized Cell Index was plotted. The Normalized Cell Index at a given time point is calculated by dividing the Cell Index at the time point by the Cell Index at a reference time point. Thus, the Normalized Cell Index is 1 at the reference time point.
  • the larger the cell index the larger the number of the cells in the wells.
  • a decrease in cell index suggests that some cells are detaching from the substrate surface or dying under the influence of the compound.
  • An increase in cell index suggests that more cells are attaching to the substrate surfaces, indicating an increase in overall cell number.
  • the present invention includes a method of monitoring cell adhesion or cell spreading including providing a microelectronic cell sensor array that displays a biological molecule or organic molecule on a test portion and a control portion, introducing a cell or cell population to the test portion and control portion, performing a series of impedance measurements of the test portion and the control portion, determining the change in impedance and optionally a cell index (CI) of the test portion and the control portion, comparing the change in impedance of the test portion to the change in impedance of the control portion or comparing the cell index (CI) of the test portion to the cell index (CI) of the control portion and determining cell adhesion or cell spreading occurs if the comparison demonstrates a significant change in impedance.
  • CI cell index
  • the device for use in monitoring cell adhesion and cell spreading has many of the features previously discussed in the present document and those incorporated by reference.
  • the device includes a non-conductive substrate, a plurality of electrode arrays positioned on the substrate, where each electrode array includes at least two electrodes and each electrode is separated from at least one electrode by an area of non-conductive material.
  • the device also includes a biological molecule or organic compound and optionally a control molecule or a control compound positioned on a portion of the substrate.
  • the non-conductive substrate may be substantially flat and may have two opposing ends along a longitudinal axis.
  • the device may have electrically conductive traces in electrical communication with at least one of the electrode arrays and extending substantially longitudinally to one of the two opposing ends.
  • the substrate may be constructed at least in part from any suitable non-conductive material such as glass, sapphire, silicon dioxide on silicon or an appropriate polymer.
  • the device may have electrodes that have a width at a widest point of more than 1.5 and less than 10 times the width of the area of non-conductive material.
  • Each electrode array may have a plurality of evenly spaced electrodes and each electrode array may be provided in any of the previously described configurations such as but not limited to interdigitated, concentric, sinusoidal, castellated and the like.
  • the methods of the present invention utilize a biological molecule or organic compound attached or closely associated with the substrate or electrode.
  • Molecules or compounds of interest may be bound or associated with the substrate or electrode to evaluate the effect on cell adhesion or cell spreading such as inducing, increasing, decreasing or inhibition.
  • the biological molecule or organic compound is attached to the substrate or electrode using techniques that utilize covalent bonds, ionic bonds, Van der Waals forces and the like.
  • the biological molecule may be directly attached or bound to the device or may be bound via an intermediate compound such as by using poly-L- lysine. Examples of binding biological molecules or organic compounds are provided in the examples.
  • the general method includes providing a microelectronic cell sensor array and incubating the biological molecule or organic compound along a portion of the substrate (such as but not limited to in a well) under conditions suitable to form a bond or to closely associate the molecule or compound with the substrate or electrode.
  • the incubation may occur utilizing a solution having an appropriate pH and salt concentration such as but not limited to phosphate buffered saline (PBS), borate buffered saline (BBS) and the like.
  • PBS phosphate buffered saline
  • BBS borate buffered saline
  • the incubation may occur at a temperature appropriate for the molecule or compound such as 4 degrees Celsius, room temperature, 37 degrees Celsius and the like.
  • the device may be washed one or more times using a suitable solution or may be blocked using a blocking solution such as a solution including a protein that does not noticeably affect the assay.
  • a blocking solution such as a solution including a protein that does not noticeably affect the assay.
  • bovine serum albumin (BSA) is provided in solution form as a blocking solution.
  • Bio molecules or organic compounds that may be of particular interest include a DNA molecule, an RNA molecule, a protein, a polypeptide, an oligopeptide, individual amino acids and the like.
  • Another example is an antibody such as a polyclonal, monoclonal or humanized antibody or a fragment thereof including light chain, heavy chain, Fc portion, Fab portion, Fab'2 portion and the like.
  • the biological molecule or organic compound may be a ligand, a receptor, may target an integrin or cell surface receptor or may be an agonist or an antagonist.
  • the biological molecule includes a molecule having an arginine-glycine- aspartic acid (RGD) motif.
  • the biological molecule or organic compound may be purified or may be provided as an extract.
  • the proteins may be isolated then bound to the substrate or electrode or alternatively, a combination of proteins may be provided in the form of an extract or unpurified mixture.
  • the display of the biological molecule or organic compound is such that a corresponding binding member or cell having the appropriate cell surface receptor is capable of recognizing and binding the molecule or compound.
  • the preferred display would likely be such that the Fab portion is positioned general! ⁇ - upwards relative to the substrate and the Fc portion positioned downwards toward the substrate.
  • the Fc portion where to be the desired binding site for a cell or protein of interest (such as but not limited to protein A) it ma ⁇ " be desired to have the Fc portion positioned generally upwards.
  • proteins, DNA. RNA, polypeptides, oligopeptides and the like are attached to the substrate of the device, it is likely that a variety of orientations will result.
  • the device includes at least one well.
  • the well acts as a fluid container to perform the analysis.
  • the well would include an electrode array and may include a biological molecule or organic compound.
  • the wells may be defined by the particular purpose such as a test well and a control well.
  • the control well provided as a control for the experiment or test and the test well typically as an experimental well.
  • both the control well and test well may include the same biological molecule or organic compound or a different biological molecule or organic compound.
  • the test well and the control well may provide a molecule or compound in the same concentration or they may be provided in different concentrations.
  • the test well and the control well contain different biological molecules or organic compounds.
  • the test well may contain a biological molecule that is suspected of having an effect on cell adhesion or cell spreading and the control well may contain a biological molecule or organic compound with a known effect on cell adhesion or cell spreading (such as increasing, decreasing or no effect).
  • the same sample of biological molecule or organic compound is aliquoted between the test well and the control well.
  • different cells may be added to the test well versus the control well, a compound such as an inhibitor or inducer may be added to one of the wells (or preincubated with the cells) or the biological molecule or organic compound may be provided at different concentrations.
  • Cells may be added directly to the devices such as in the test well or control well or may be preincubated with one or more compounds. Preincubation may be desired when assaying for an inhibitor of cell adhesion or cell spreading. Alternatively, the inhibitor or other compound of interest may be added to the device at the same time as the cell or cell population or may be added later.
  • the types of cells that may be used to monitor cell adhesion or cell spreading may vary.
  • T) 7 PiCaIIy a cell type or cell line capable of adhering to the device, the biological molecule or the electrode would be desired.
  • Cells may be from an ⁇ ' suitable organism such as human, bovine, hamster, swine, and the like. The cells ma ⁇ ' be prokaryotic or eukaryotic.
  • Cells ma ⁇ 7 be primarly cells or cell lines. Human cells or cell lines derived from human cells have a particular utility. Cells may be those associated with the immune system such as B-lymphocytes, T-lymphocytes, macrophages, granulocytes, mast cells and PBMCs.
  • a series of impedance measurements are performed to detect changes in cell adhesion or cell spreading.
  • Impedance may be measured at regular time intervals, irregular time intervals, or a combination thereof. Time intervals of interest may be 1) after coating a device with a biological molecule or compound of interest and before adding cells, 2) shortly after adding cells and 3) one or more measurements over time. However alternative time points may be desired.
  • the impedance of the test portion such as the test well and control well are preferably taken simultaneously or nearly simultaneously.
  • the impedance values between the test portion and the control portion may be compared or corresponding cell indexes may be compared to one another to determine changes in cell adhesion or cell spreading.
  • Cell substrate impedance measurement is directly related to the number of cells added to the electrodes and the electrode area covered by the cells. During cell adhesion experiments the number of cells added to each well is fixed and therefore the change in impedance is primarily derived from the degree of cell attachment and spreading on the electrode surface. Therefore as the suspended cells settle onto the surface of the electrode, adhere and undergo morphological transformation, the cell substrate impedance increases proportionately with the area of the electrode covered by the cell. In addition, the strength of attachment, which may depend on the cell attachment receptors expressed on the surface of the cell or the biological molecule coated onto the surface of the electrode can also affect cell electrode impedance measurements.
  • the methods of the present invention may include comparing one or more impedance measurements or comparing one or more cell indexes or cell index values.
  • a cell index is determined by calculaiing, for each measurement frequency. the relative-change in resistance (a component of impedance) of a well when target cells are present in the well with respect to that of the well when no cell is present and then finding the maximum relative-change in resistance for all frequencies measured. The maximum relative-change in resistance is used as cell index (see equation (4) in Section C. Methods for Calculating Cell Index (CI) and CeU Change Index (CCI) of the present invention).
  • impedance is measured_at a single frequency, then the relative change in resistance (a component of impedance) of a well when cells are present in the well with respect to that of the well when no cell is present.
  • Other methods for calculating cell index have been disclosed in a previous Section C. Methods for Calculating Cell Index (CI) and Cell Change Index (CCI) of the present invention).
  • Example 1 Coating a Microelectronic Plate with a.Biological Molecule or Organic Compound including Extracellular Matrix (ECM) Protein
  • Mammalian cells express membrane -bound receptors called integrins which interact with ECM proteins in a specific manner. Upon interaction of integrins with their cognate ECM proteins, a signaling cascade is initiated inside the cell leading to attachment, spreading, growth, differentiation and morphological dynamics depending on the integrin and the ECM substrate. Coating of ACEA E-plates with ECM proteins will allow label-free, quantitative and real-time measurements of cellular interaction with the ECM protein using the RT-CES system.
  • the steps involved in coating a microelectronic plate, such as the ACEA E-plates, and determining cellular response may include the following steps:
  • the plate was placed at 37 0 C for lhour to allow coating to take place followed with PBS wash and then 50 ⁇ L of media was added to E-plate to measure the background impedance.
  • 5000 NIH3T3 cells in 100 ⁇ L volume were then added to the wells and the plates were placed on the device station in the 37 0 C.
  • the attachment and spreading of NIH3T3 cells on the two different surfaces were then monitored every 5 minutes using the RT-CES system (FIG. 1).
  • the kinetic trace of NTH3T3 cells on FN shows an immediate increase in cell index which correlates with the attachment and spreading of these cells while on PLL it is steady increase overtime.
  • NIH3T3 cells on FN The attachment and spreading of NIH3T3 cells on FN is a rapid process and takes place within 5 minutes of adding the cells to the coated wells (FIG. 2).
  • the cells spread for approximately an hour at which time they contract due to stress fiber formation.
  • the cells attach non- specifically due to charge interaction between PLL and the negatively charged proteins on the cell membrane.
  • PLL cell spreading does not take place for at least the first two hours after which the cells spread due to the fact that they secrete their own matrix.
  • the wells of ACEA E-plates were coated with increasing amounts of FN in the range of 0 ⁇ g/mL to 20 ⁇ g/mL and the attachment and spreading of NIH3T3 cells were monitored by the RT- CES (FIG. 3).
  • the kinetic measurements for attachment and spreading clearly indicate that with increasing amounts of FN being coated on the wells, the index of cell attachment and spreading increases accordingly.
  • arginine- glycine-aspartic acid (RGD) peptides were added to the wells in increasing concentration prior to adding the cells. As shown in FIG.
  • Example 2 Coating a Microelectronic Plate with a Biological Molecule or
  • the wells of ACEA E-plates can also be coated with other biological molecules such as antibodies specific for a particular receptor present on the cell surface. These antibodies can be functional antibodies (triggering a specific cellular response) or non-functional antibodies. The main requirement being that they recognize and bind to specific epitopes within the receptor of interest at the cell surface.
  • the wells of ACEA E-plate with the OKT-3 antibody which is specific for the CD3 co-receptor of the T cell receptor complex.
  • OKT-3 is a functional antibody and upon binding to the CD3 co-receptor on T lymphocytes triggers a signaling pathway leading to activation and adhesion of the T cell.
  • the wells were also coated with an irrelevant mouse monoclonal antibody.
  • the wells coated with the OKT-3 upon addition of Jurkat T cells, which express the CD-3 receptor, to the wells coated with the OKT-3, the cells immediately attach and spread as evidenced by an immediate increase in cell index.
  • the control antibody very little attachment and spreading is taking place.
  • the following steps provide a method of coating microelectronic plate (the ACEA E-plate) wells with an antibody specific for cell surface receptors:
  • Example 3 Coating a Microelectronic Plate with a Biological Molecule or
  • the wells in ACEA E-plates can also be coated covalently or non-covalently with specific peptides, ligands or compounds which can illicit some specific cellular response such as adhesion and spreading.
  • specific peptides, ligands or compounds which can illicit some specific cellular response such as adhesion and spreading.
  • RGD containing peptides when coated upon a surface are sufficient to promote attachment and spreading of cells via interaction with specific integrin receptors on the cell surface.
  • NTH3T3 cells were maintained in DMEM media containing 10 % FBS and 1% penicillin and streptomycin.
  • Jurkat T cells and BxPC3 cells were maintained in RPMI containing 10 % FBS and 1 % penicillin and strptomycin.
  • ACEA e-plates were coated with the indicated ECM protein or PLL for 1 hour at 37 0 C. The plates were washed with PBS and coated with 0.5% BSA solution in PBS for 20 minutes at 37 0 C. The wells were washed with PBS prior to addition of the media and cells. The cells were trypsinized, spun and resuspended in serum-free media containing 0.25% BSA. The cells were adjusted to appropriate concentration and 100 ⁇ L of the cell suspension was transferred to the wells of ACEA e-plates coated with the various ECM proteins.
  • the adhesion and spreading of the cells were monitored continuously every 3 minutes using the RT-CES system for a period of 1-3 hours depending on the experiment.
  • the electronic readout, cell sensor impedance is displayed as an arbitrary unit called the Cell Index (CI) where the CI is defined as R n -Rb/R D ; R n is defined as the cell -electrode impedance of the well with the cells at a particular time point and Rb is defined as the background impedance of the wells with just the media alone.
  • CI Cell Index
  • BxPc3 cells were transfected with 20 nM of siSRC using siPORT amine at a final volume of 60 ⁇ L. Cells were assayed for adhesion function 48 hours after transfection.
  • the cells were seeded in 16X chamber slides coated with either PLL or FN. The cells were allowed to attach and were fixed with 4% parafarmaldehyde at the indicated time points. The cells were pe ⁇ neabilized, stained with rhodarnine-phalloidin (Molecular Probes), visualized and photographed using a Nikon E- 400 epi-fluorescent microscope connected to a digital camera.
  • ACEA E-plates were coated with FN or PLL as a control.
  • NIH3T3 cells were applied onto the coated wells and the extent of adhesion and spreading was monitored by the RT- CES system.
  • chamber slides were also coated with FN and PLL and the same numbers of cells were added to each well and its attachment and spreading were determined by staining with rhodamine-phalloidin and visualization by using the epifluorescent microscope.
  • FIG. 6 application of the cells onto the FN- coated wells leads to a dramatic increase in cell index whereas on PLL it leads to steady increase overtime.
  • immunofluorescent images show that cell attachment on FN is accompanied by immediate spreading which is maximal by 1 hour (FIG. 6A). On PLL coated wells, the cells tend to remain round even up two hours after initial attachment (FIG. 6A).
  • ACEA E-plates were coated with increasing concentration of FN ranging from 0 ug/mL to 20 ⁇ g/mL.
  • NTH3T3 cells were added to the wells and the extent of attachment and spreading was monitored using the RT-CES system.
  • the CI increases proportionately with increasing amounts of coated FN.
  • the cells were trypsinized at 3 hours post-adhesion and manually counted.
  • the actual raw cell number at three hours for the different FN concentrations is proportional to the CI obtained at three hours.
  • Integrm heterodimers such as ⁇ 5 ⁇ l integrins which bind to FN recognize specific motif in FN, the arginine-glycine-aspartic acid (RGD) motif (i). It has been shown peptides containing the RGD motif can effectively compete for the binding of cells expressing the FN receptor to FN (2).
  • RGD arginine-glycine-aspartic acid
  • NIH3T3 cells were detached and incubated in the presence of increasing amounts of cyclic-RGD peptides (FIG. 8A) and then plated onto FN-coated E-plates and monitored by the RT-CES system. As seen in FIG.
  • Example 6 Inhibition of Cell Attachment and Spreading Using Actin-Disrupting Agents or Compounds and Specific Inhibitors of Signaling Proteins Involved In Attachment and Spreading
  • Integrin-mediated cell adhesion is known to organize the actin cytoskel ⁇ ton in a specific manner. Vise versa, the actin cytoskel ⁇ ton also participates in organizing integrins and other intracellular signaling proteins into signaling modules which regulates cell attachment and spreading (i).
  • NTH3T3 cells were detached and pre-incubated with increasing concentrations of Latriculin, which is a potent inhibitor of actin polymerization. The cells were then seeded onto FN-coated wells in ACEA E-plates and the extent of adhesion and spreading was monitored using the RT-CES system. As shown in FIG. 9A, Latriculin inhibits cell attachment and spreading in a concentration- dependent manner. Analysis of the extent of cell attachment and spreading at two hours, clearly demonstrates that Latriculin is a potent inhibitor of cell attachment and spreading (FIG. 9B).
  • Src family of non-receptor tyrosine kinases One of the main signaling proteins which participates in integrin-mediated cell attachment and spreading is the Src family of non-receptor tyrosine kinases (7).
  • BxPC3 cells were pre-incubated with the Src kinase inhibitor PP2 and then seeded onto FN-coated wells in ACEA E-plate. The extent of cell attachment and spreading was monitored using the RT-CES system. As shown in FIG. 10, cell attachment and spreading is significantly inhibited in the presence of the Src inhibitor. At two hours. after seeding the cells treated with the PP2 compound displayed an approximately 60 % inhibition of cell attachment and spreading relative to DMSO treated cells. This finding confirms previous results using conventional methods to assess cell attachment and spreading in the presence of the Src family inhibitor (3).
  • BxPC3 cells were transfected with a control siRNA or a siRNA specific for the c-Src mRNA. Forty eight hours after transfection, the cells were detached and seeded onto FN-coated wells in ACEA E-plate and the extent of cell adhesion and spreading was monitored using the RT-CES system. As shown in FIG. HA and B, down regulation of the c-Src gene product leads to a 30 % decrease in cell attachment and spreading at two hours post-cell seeding.
  • the RT-CES system can monitor and assess cell attachment and spreading quantitatively, under label-free conditions and in real-time. The preclusion of labeling saves on expensive reagents and time.
  • the other major advantage of using the RT-CES system is that since the readout is non-invasive, the user, in addition to monitoring the effect of matrix proteins on adhesion and spreading can continue to monitor its effect on other biological events such as differentiation or proliferation. Using traditional methods, it would have been necessary to perform separate experiments for each of these events.

Abstract

La présente invention concerne des dispositifs et des méthodes de surveillance dynamique de l'adhésion cellulaire et de la diffusion cellulaire. Les cellules sont ajoutées dans un réseau de détection cellulaire microélectronique connecté à un analyseur d'impédance. Le dispositif comprend également un revêtement contenant une molécule biologique ou un composé organique pouvant interagir avec la cellule. L'adhésion cellulaire et la mobilité cellulaire sont déterminées par détection des changements d'impédance, et comparaison de l'impédance ou des valeurs d'indice cellulaire entre les échantillons.
EP05812268A 2004-09-27 2005-09-27 Surveillance dynamique de l'adhesion et de la diffusion cellulaire a l'aide du systeme rt-ces Withdrawn EP1800312A4 (fr)

Applications Claiming Priority (24)

Application Number Priority Date Filing Date Title
US61374904P 2004-09-27 2004-09-27
US61387204P 2004-09-27 2004-09-27
US61460104P 2004-09-29 2004-09-29
PCT/US2004/037696 WO2005047482A2 (fr) 2003-11-12 2004-11-12 Systemes de detection de cellules electroniques en temps reel pour des epreuves a base de cellules
US10/987,732 US7192752B2 (en) 2002-12-20 2004-11-12 Real time electronic cell sensing systems and applications for cell-based assays
US63007104P 2004-11-22 2004-11-22
US63013104P 2004-11-22 2004-11-22
US63080904P 2004-11-24 2004-11-24
US63301904P 2004-12-03 2004-12-03
US64715905P 2005-01-26 2005-01-26
US64718905P 2005-01-26 2005-01-26
US64707505P 2005-01-26 2005-01-26
PCT/US2005/004481 WO2005077104A2 (fr) 2004-02-09 2005-02-09 Systemes de detection de cellules electroniques en temps reel et applications en matiere de profilage de cytotoxicite et dosages de composes
US11/055,639 US7560269B2 (en) 2002-12-20 2005-02-09 Real time electronic cell sensing system and applications for cytotoxicity profiling and compound assays
US65390405P 2005-02-17 2005-02-17
US66089805P 2005-03-10 2005-03-10
US66082905P 2005-03-10 2005-03-10
US67367805P 2005-04-21 2005-04-21
US68942205P 2005-06-10 2005-06-10
PCT/US2005/027891 WO2006015387A2 (fr) 2004-08-04 2005-08-04 Procede de dosage de la destruction de cellules cibles par des cellules tueuses naturelles, des lymphocytes t cytotoxiques et des neutrophiles, a l'aide de la technique de detection micro-electronique de cellules en temps reel
US11/198,831 US8263375B2 (en) 2002-12-20 2005-08-04 Dynamic monitoring of activation of G-protein coupled receptor (GPCR) and receptor tyrosine kinase (RTK) in living cells using real-time microelectronic cell sensing technology
US11/197,994 US7468255B2 (en) 2002-12-20 2005-08-04 Method for assaying for natural killer, cytotoxic T-lymphocyte and neutrophil-mediated killing of target cells using real-time microelectronic cell sensing technology
PCT/US2005/027943 WO2006017762A2 (fr) 2004-08-04 2005-08-04 Controle dynamique de l'activation de la proteine g (gpcr) et de recepteur tyrosine kinase (rtk) dans des cellules vivantes mettant en oeuvre la technologie de detection micro-electronique de cellules en temps reel
PCT/US2005/034561 WO2006036952A2 (fr) 2004-09-27 2005-09-27 Surveillance dynamique de l'adhesion et de la diffusion cellulaire a l'aide du systeme rt-ces

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EP2199783A1 (fr) * 2008-12-17 2010-06-23 Koninklijke Philips Electronics N.V. Dispositif microélectronique pour la mesure de l'adhésion cellulaire
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US5981268A (en) * 1997-05-30 1999-11-09 Board Of Trustees, Leland Stanford, Jr. University Hybrid biosensors
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