WO2008102118A1 - Large scale production of stem cells - Google Patents
Large scale production of stem cells Download PDFInfo
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- WO2008102118A1 WO2008102118A1 PCT/GB2008/000558 GB2008000558W WO2008102118A1 WO 2008102118 A1 WO2008102118 A1 WO 2008102118A1 GB 2008000558 W GB2008000558 W GB 2008000558W WO 2008102118 A1 WO2008102118 A1 WO 2008102118A1
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- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/0603—Embryonic cells ; Embryoid bodies
- C12N5/0606—Pluripotent embryonic cells, e.g. embryonic stem cells [ES]
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/0618—Cells of the nervous system
- C12N5/0623—Stem cells
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2531/00—Microcarriers
Definitions
- the present invention relates to methods for large-scale production of stem cells, including pluripotent and embryonic stem cells.
- the invention also relates to methods for large-scale production of differentiated cells derived from stem cells in culture.
- the invention also relates to the use of stem cells or the differentiated progeny thereof in assays, for example for drug discovery.
- stem cell cultures in vitro including cultures of pluripotent stem cells such as embryonic stem (ES) cells, is well known.
- pluripotent stem cell cultures in the presence of medium containing serum and Leukaemia Inhibitory Factor (LIF) is described in Smith et al. (1988) Nature 336: 688-90.
- LIF Leukaemia Inhibitory Factor
- Stem cell cultures can also be induced to differentiate in vitro and hence provide a source of differentiated cell types, including progenitor and stem cells, which are otherwise difficult to obtain.
- mouse ES cell lines can be expanded in vitro and have the ability to give rise to cells from all three germ layers (Smith (2001) Annu Rev Cell Dev Biol 17: 435-462).
- stem cell lines and specific differentiated cell types can offer the drug discovery community a cell culture model that is more physiologically relevant than immortalised cell lines and that avoids the expense and time of in vivo experiments and the development of animal models.
- stem cells are to be widely adopted as research tools it will be necessary to develop culture processes for stem cell growth and differentiation that reliably and reproducibly yield the quantity and quality of cells required.
- high throughput screening assays in which millions of compounds are screened, the number of cells required would be in the order of billions of cells per day.
- Fok and Zandstra ((2005) Stem Cells 23: 1333-1342) describe 50ml cultures of mouse ES cells on microcarriers in 100ml spinner flasks. However, such cultures exhibited increased population doubling times and reduced cumulative fold expansion when compared to tissue culture flask controls. In addition, significant "bead-bridging" (i.e. formation of aggregates of microcarriers and cells) was acknowledged to lead to creation of a suboptimal culture environment.
- a first aspect of the invention provides a method for large-scale production of pluripotent stem cells, suitably embryonic stem (ES), embryonic carcinoma (EC), embryonic gonadal (EG) cells, induced pluripotent stem (iPS) cells or reprogrammed cells, comprising:
- the invention also provides a method for large-scale production of stem cells other than mouse ES cells comprising:
- Such methods may be used to culture any type of stem cell that is of interest including mouse stem cells and human stem cells.
- Other mammalian stem cells can also be cultured according to the methods of the invention, including rat, American mink, hamster, pig, sheep, cow and primate stem cells.
- stem cell embraces any cell having the capacity for self-renewal and the potential to differentiate into one or more other cell types.
- stem cell includes pluripotential, multipotential or unipotential stem cells and progenitor cells from any tissue or stage of development.
- the desired stem cells may be ES cells, EC cells, EG cells, iPS cells, reprogrammed cells, haematopoietic stem cells, epidermal stem cells, mesenchymal stem cells, adipose tissue-derived stem cells, muscle stem cells or neural stem cells.
- the methods described herein are suitable for use with media containing serum and with serum-free media.
- the culture medium is serum-free.
- the replacement of serum or other incompletely defined or undefined medium components with defined medium components can also result in greater reproducibility of the methods of the invention.
- a number of suitable culture media are commercially available for the culture of stem cells and are suitable for use in the methods of the invention.
- the medium used to expand populations of stem cells according to the methods of the invention will be the same medium used for conventional culture in plates or tissue culture flasks.
- a different medium may be used in the methods of the invention of the medium may be supplemented with additional components that promote proliferation or survival of the stem cells and/or prevent differentiation.
- the medium may, in some embodiments, comprise a combination of a MEK inhibitor, a GSK3 inhibitor and, optionally, an antagonist of an FGF receptor. This combination is the subject of a co- pending patent application, GB0615327.4, filed on 1 August 2006, the contents of which are incorporated herein by reference.
- GSK3 inhibition refers to inhibition of one or more GSK3 enzymes.
- the family of GSK3 enzymes is well-known and a number of variants have been described (see e.g. Schaffer et al.; Gene 2003; 302(1-2): 73-81).
- GSK3- ⁇ is inhibited.
- GSK3- ⁇ inhibitors are also suitable, and in general inhibitors for use in the invention inhibit both.
- a wide range of GSK3 inhibitors are known, by way of example, the inhibitors CHIR 98014, CHIR 99021, AR-AO144-18, TDZD-8, SB216763 and SB415286. Other inhibitors are known and useful in the invention.
- the inhibitors of certain embodiments are specific for GSK3- ⁇ and GSK3- ⁇ , substantially do not inhibit erk2 and substantially do not inhibit cdc2.
- the inhibitors Preferably have at least 100 fold, more preferably at least 200 fold, very preferably at least 400 fold selectivity for human GSK3 over mouse erk2 and/or human cdc2, measured as ratio of IC 50 values; here, reference to GSK3 IC 50 values refers to the mean values for human GSK3- ⁇ and GSK3- ⁇ . Good results have been obtained with CHIR 99021 and CHIR 98014, which are both specific for GSK3. Examples of GSK3 inhibitors are described in Bennett C, et al, J. Biol. Chem., vol. 277, no.
- Suitable concentrations for use of CHIR 99021 are in the range 0.01 to 100, preferably 0.1 to 20, more preferably 0.3 to 10 micromolar.
- MEK inhibitors refers to MEK inhibitors in general.
- reference to a MEK inhibitor refers to any inhibitor a member of the MEK family of protein kinases, including MEK1 , MEK2 and MEK3.
- suitable MEK inhibitors include the MEK1 inhibitors PD184352 and PD98059, inhibitors of MEK1 and MEK2 U0126 and SL327, and those discussed in Davies et al (2000) (Davies SP, Reddy H, Caivano M, Cohen P.
- RNA- mediated interference RNA-mediated interference
- RNAi RNA-mediated interference
- a double-stranded RNA molecule complementary to all or part of a MEK gene is introduced into pluripotent cells, thus promoting specific degradation of MEK-encoding mRNA molecules. This post-transcriptional mechanism results in reduced or abolished expression of the targeted MEK gene.
- Suitable techniques and protocols for achieving MEK inhibition using RNAi are known.
- a number of assays for identifying kinase inhibitors are known.
- Davies et al (2000) describe kinase assays in which a kinase is incubated in the presence of a peptide substrate and radiolabeled ATP. Phosphorylation of the substrate by the kinase results in incorporation of the label into the substrate. Aliquots of each reaction are immobilized on phosphocellulose paper and washed in phosphoric acid to remove free ATP. The activity of the substrate following incubation is then measured and provides an indication of kinase activity.
- the relative kinase activity in the presence and absence of candidate kinase inhibitors can be readily determined using such an assay.
- Downey et al. (1996) J Biol Chem.; 271(35): 21005-21011 also describes assays for kinase activity which can be used to identify kinase inhibitors.
- optimum culture conditions are maintained throughout the culture as, for example, sub-optimal conditions can induce spontaneous differentiation of pluripotent cells.
- the culture of step d) is subjected to agitation in order to avoid the development of localised regions of sub-optimal culture conditions, for example due to microcarriers settling at the bottom of the culture vessel.
- Agitation of the culture medium also advantageously allows the stem cells to be cultured at higher densities than is possible in tissue culture flasks.
- the use of microcarriers provides an increased surface area for cell growth whilst agitation ensures that there is adequate distribution of nutrients and oxygen to all cells in the culture.
- 1 L of culture can yield as many stem cells as 70 to 100 T-175 tissue culture flasks maintained using conventional methods. Agitation can be achieved in a number of ways, including the use of spinner flasks containing a magnetic paddle or impeller. Alternatively, the methods of the invention can be carried out in a bioreactor. A number of types of bioreactor are available, including bioreactors in which agitation of the medium is achieved using a paddle or impeller and rotary wall bioreactors. Rotary wall bioreactors can additionally be used to simulate conditions of reduced gravity (microgravity) which, in some embodiments, may promote desirable cell growth or differentiation characteristics.
- microgravity reduced gravity
- An advantage of using a bioreactor is that one or more culture parameters can be monitored and/or controlled, either continuously or at intervals determined by the user.
- the monitoring can be carried out using probes inserted into the culture vessel.
- a medium sample can be withdrawn from the culture vessel and analysed.
- one or more of the oxygen concentration, the pH, the concentration of glucose, the concentration of lactate, and the shear rate are controlled. This allows optimum or near- optimum culture conditions to be maintained spatially and temporally for the duration of the culture, for example by varying one or more culture parameters.
- a number of parameters are important for maintaining and expanding stem cells in large-scale cultures, including temperature, oxygen concentration, pH, concentrations of nutrients (e.g. glucose) and waste products (e.g. lactate), and shear rate.
- temperature at which mammalian stem cells are cultured is about 37 0 C + 0.5 0 C, although the skilled person will appreciate that wider variations of temperature might be possible in some embodiments.
- temperature is controlled by placing the culture vessels in temperature-controlled incubators or, in the case of some bioreactors, by direct monitoring and control of the temperature in the culture vessel. Temperature variations can be minimised by ensuring all media and culture components are brought to the required temperature before being added to the culture vessel.
- oxygen supply is increased by means of agitation of the medium, e.g. as described herein, to increase the amount of oxygen dissolved in the medium.
- the source of oxygen will be the headspace of the culture vessel, and the rate of agitation will be selected so as to ensure adequate oxygen supply to the cells without generating a shear rate that damages or impairs the growth of the cells.
- Gas exchange in the headspace is generally achieved by direct supply of gas to the culture vessel or by use of vented culture vessels in gassed incubators. In both cases, the gas supply is usually approximately 5% CO 2 in air. Some variation in the proportion of CO 2 in the gas is possible, e.g. +/- 1% or +/- 2%. Other methods for supplying oxygen to stem cell cultures of the invention are also possible, e.g. sparging. In particular, oxygen can be passed through gas permeable tubing into the liquid in the bioreactor, thus minimising damage to the cells due to the formation of bubbles during sparging.
- the pH of the culture medium can also be monitored and/or controlled in order to maintain optimal culture conditions. Control of pH can be achieved by any suitable method, including replacement of all or a portion of the culture medium or direct addition of pH-adjusting agents to the medium. pH is commonly controlled by gassing the headspace or the culture media with 5- 7% CO 2 in air.
- the concentrations of nutrients and/or waste products can be monitored and/or controlled.
- glucose concentration is monitored to provide an indication of the nutrients available to the stem cells.
- lactate concentration is monitored to provide an indication of the levels of waste products in the medium that might reduce cell survival, growth or proliferation.
- the presence of nutrients and waste products in the culture medium can be controlled by replacement of all or a portion of the culture medium.
- Nutrients can also be provided by the addition of specific medium components or additional medium to the stem cell cultures.
- shear forces are controlled by adjusting the stirring rate (e.g. by reducing or increasing the speed of the paddle or impeller).
- the shear rate can also be used to control the aggregation of cells within the cultures.
- the shear rate is increased with time in culture to compensate for the increasing weight of the microcarriers caused by proliferation of attached cells. This advantageously counters the tendency of the microcarriers to settle under gravity and avoids excess shear at early stages of the culture, thus maintaining optimum culture conditions and reducing or eliminating the formation of aggregates of microcarriers and cells.
- step d) of the method preferably comprises periodic replacement of a proportion of the medium volume with fresh medium.
- the proportion of medium volume replaced will vary between different embodiments of the invention and may be 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 90% of the culture volume.
- the frequency of medium replacement can also vary, and may be, for example, every 12, 24, 36 or 48 hours. The precise proportions and frequencies chosen in different embodiments will depend on the type of cells being cultured, the culture medium, the type of culture vessel, and other culture parameters, and can be readily determined by the user.
- the total culture volume will be in excess of about 100 ml, 250 ml, 500 ml or 1000 ml.
- the maximum culture volume is in principle without limit, provided that culture parameters such as oxygen concentration and pH are controlled.
- bioreactors having a culture capacity of 70,000 L are known. It is noted that the total volume of the culture vessel will, in general, significantly exceed the culture volume. In specific examples described herein, the total culture volume is approximately half of the total volume of the culture vessel.
- the excess volume in the culture vessel forms a headspace which provides a source of oxygen, as described above.
- the medium is continually replenished, i.e. fresh medium is continually added and used medium is continually removed.
- fresh medium is continually added and used medium is continually removed.
- Continuous perfusion methods of the invention will typically monitor the concentration of glucose or lactate in the culture medium and vary the rate of medium replacement in order to keep the glucose or lactate concentration at a value or within a range determined by the user.
- other parameters or combinations of parameters described herein may be used to control the rate of medium replacement.
- stem cells in particular, it may be beneficial to maintain levels of growth factors or cytokines which can supplement the media and contribute to maintenance of the stem cell phenotype.
- the stem cells are typically inoculated into a relatively small first volume of medium containing microcarriers, and the medium volume increased to the total culture volume after the stem cells have adhered to the microcarriers.
- the first volume can be about 5%, 10%, 20%, 30%, 40% or 50% of the total (final) culture volume.
- satisfactory results can be obtained when the first volume is equal to the total culture volume, i.e. without increasing the culture volume after the stem cells have been allowed to adhere to the microcarriers.
- the first volume of culture medium is inoculated with pluripotent cells or other stem cells in suspension.
- the suspension may comprise single cells or small clusters of stem cells. Typically, the clusters of stem cells will each contain from about 10 to about 20 or 30 cells.
- the inoculated stem cells are not in single cell suspension as this leads to reduced survival of the stem cells in subsequent culture.
- stem cell including some pluripotent human cells, it is found that dissociation into single cells tends to lead to cell death. However, survival in subsequent culture is significantly improved if clumps of stem cells are used to inoculate the cultures.
- Periodic or continuous agitation of the first volume of culture medium may be carried out whilst the stem cells are being permitted to adhere to the microcarriers to aid uniform distribution of the stem cells across the microcarriers.
- stem cells inoculated will depend on the type of stem cell and the total final culture volume. In the specific examples described herein, stem cells have been inoculated at 5 x 10 4 1 x 10 5 cells/ml final culture medium and successfully expanded using the methods of the invention.
- stem cells are most effective when the initial population of stem cells inoculated into the culture medium is of high quality. It is preferred that the stem cells for inoculation are not confluent and are in log phase growth.
- the cultures of stem cells from which the inoculum is obtained should therefore be passaged sufficiently in advance of inoculation to ensure that the cells are in good condition. The precise timing will depend on the type of stem cell and the doubling time obtained in the particular culture conditions used. Typically, for mouse ES cells, passaging the cells 24 hours in advance of inoculation will result in non-confluent cells in log phase growth.
- microcarriers A number of types of microcarriers are commercially available and suitable for use in the methods of the invention, including Cytodex 1 , Cytodex 3 (Amersham Biosciences), 2D Microhex (Nunc) and Cultispher (Percell Biolytica).
- Microcarriers may be made of tissue culture plastic, dextran or gelatin and may be coated with collagen or gelatin. The microcarriers may be supplied pre-coated or the coating can be applied by the user using standard methods. In some applications of the invention, particular types of microcarriers will be particularly suitable, e.g. biocompatible, biodegradable and/or animal component-free microcarriers.
- microcarriers have diameters of 1mm or less, preferably 500 ⁇ m or less and often in the range 30-300 ⁇ m
- the microcarriers can be processed according to the manufacturer's directions. Typically, the microcarriers will be sterilised and washed in buffer and/or culture medium before the cultures of the invention are set up. In preferred embodiments, the microcarriers are sterilised by autoclaving in phosphate buffered saline (PBS) and, if necessary, stored at 4 0 C until required. Before use, the microcarriers are washed in fresh PBS and then washed or preferably soaked in culture medium at 37 0 C, typically for about 1 hour. In the hands of the present inventors, soaking the microcarriers in medium prior to use has yielded particularly good results.
- PBS phosphate buffered saline
- microcarrier densities are about 0.5 - 1 g/litre (Cultispher microcarriers) and about 1 g/litre (Cytodex microcarriers).
- the additional step of e) harvesting the stem cells is carried out.
- the stem cells there is no need to separate the stem cells from the microcarriers and the microcarriers are simply separated from the culture medium. This can be achieved by any suitable method, e.g. filtration. However, it is particularly convenient to allow the microcarriers and attached cells to settle to the bottom of the culture vessel in the absence of agitation, decant or aspirate off surplus culture medium, and transfer the microcarriers to an appropriate vessel.
- the harvesting comprises a) isolating the microcarriers from the culture medium; and b) separating the stem cells from the microcarriers.
- the stem cells can be separated from the microcarriers using an enzymatic or non-enzymatic cell dissociation reagent.
- Suitable cell dissociation reagents include trypsin-EDTA, Accutase (Chemicon) and Cell
- the microcarriers are soluble in the cell dissociation reagent, thus enabling convenient isolation of the stem cells without the need to remove the microcarriers in an additional step.
- gelatin microcarriers are soluble in trypsin-EDTA.
- the methods of the invention are suitable for production of feeder-dependent stem cells as well as feeder-independent/feeder-free cultures. This is of particular value for expanding feeder-dependent human ES cell lines, as described in the specific examples, although other feeder-dependent stem cells can be cultured according to the invention.
- the feeder cells are inoculated into medium containing a plurality of microcarriers and are permitted to adhere to the microcarriers prior to the inoculation of step a).
- the feeder cells are permitted to proliferate until confluence prior to the inoculation of step a). It is also preferred that the feeder cells are inactivated prior to the inoculation of step a), for example using known protocols for ⁇ -irradiation or mitomycin c treatment.
- the methods of the invention can also be adapted to permit the large-scale production of differentiated cells derived from stem cells.
- Such methods advantageously permit the production of large, and potentially limitless, numbers of cells of a desired phenotype by means of in vitro differentiation of stem cells. Potentially any cell type, even cell types that are rare in vivo, can be provided reproducibly and in large numbers.
- the invention provides a method for large-scale production of desired differentiated cells derived from stem cells comprising: a) providing a suspension of particles comprising the stem cells adhered to microcarriers in culture medium; and b) inducing differentiation of the stem cells on the microcarriers.
- the invention provides a method for large-scale production of desired differentiated cells derived from stem cells comprising:
- the culture medium is serum-free.
- the methods of the invention can be used to produce large populations of multipotential or unipotential stem cells and terminally differentiated cells of a given phenotype by directing differentiation of the inoculated stem cells along one or more lineage pathways.
- the differentiated cells can for example be somatic stem cells, haematopoietic stem cells, epidermal stem cells, mesenchmal stem cells, adipose tissue-derived stem cells, muscle stem cells or neural stem cells.
- the differentiated cells are a mixed population of cells belonging to one or more desired lineages.
- the differentiated cells are neural cells. As a specific example, they are neurons.
- step d) comprises (i) incubating the culture under conditions conducive to the proliferation of the stem cells and (ii) incubating the culture under conditions conducive to the differentiation of the stem cells into the desired differentiated cells.
- the methods for production of differentiated cells of the invention are generally carried out under similar conditions to those used for producing stem cells according to the first aspect of the invention.
- the culture of step d) is preferably subjected to agitation, as described herein, and one or more of the oxygen concentration, the pH, the concentration of glucose, the concentration of lactate, and the shear rate are controlled.
- methods of the invention for producing differentiated cells preferably comprise inoculating the first volume of culture medium with ES cells or other stem cells in suspension.
- the suspension may comprise single cells or clusters of stem cells, for example clusters of stem cells each containing from about 10 to about 20 or 30 cells.
- step d) can comprise periodic replacement of a proportion of the medium volume with fresh medium, as described above.
- the proportion of the medium volume can be 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 90% and the medium can be replaced every 12, 24, 36 or 48 hours.
- Continuous perfusion methods as described herein are also suitable for the production of differentiated cells.
- the total culture volume is in excess of about 100 ml, 250 ml, 500 ml or 1000 ml.
- the methods for producing differentiated cells according to the invention preferably comprise the step of e) harvesting the desired differentiated cells.
- Harvesting the differentiated cells may be carried out using the methods described for harvesting stem cells.
- harvesting may comprise a) isolating the microcarriers from the culture medium; and b) separating the differentiated cells from the microcarriers.
- the differentiated cells can be separated from the microcarriers using an enzymatic or a non-enzymatic cell dissociation reagent, for example trypsin- EDTA.
- the microcarriers are soluble, more preferably in the cell dissociation reagent.
- the harvested cells, or a proportion thereof are used to seed one or more further cultures as described herein. This step can be repeated, as desired, to create a continuous supply of differentiated cells.
- feeder cells are permitted to adhere to the microcarriers prior to the inoculation of step a).
- the feeder cells are permitted to proliferate until confluence prior to the inoculation of step a). It is also preferred for the feeder cells to be inactivated prior to the inoculation of step a).
- the yield of stem cells or differentiated cells obtained using the methods of the invention will vary according to the culture conditions, culture volume and the initial and final cell types. However, in the specific examples production of populations of 5 x 10 7 - 10 8 and 1 - 1.5 x 10 8 mouse ES cells (1-2 x 10 6 and 2-3 x 10 6 cells/ml). Similar yields of mouse neural stem cells have also been obtained using the methods of the invention. Preferably, the yield of stem cells or differentiated cells represents a 10-fold, 20-fold, 50-fold or even 100- fold or greater expansion of the originally inoculated cell population.
- a further aspect of the invention provides a population of differentiated cells obtainable by the methods of the second and third aspects of the invention.
- the population comprises at least about 10 8 cells. Larger populations of cells can be obtained according to the invention, for example populations of at least 5 x 10 8 , 10 9 or 10 10 cells.
- the population of cells is frozen using conventional cryopreservation techniques.
- the invention provides a composition comprising the differentiated progeny of stem cells attached to microcarriers.
- the differentiated progeny can be somatic stem cells, haematopoietic stem cells, epidermal stem cells, mesenchymal stem cells, adipose tissue-derived stem cells, muscle stem cells or neural stem cells, and may be a mixed population of cells belonging to one or more lineages.
- the differentiated progeny are neural cells.
- the invention also provides a composition comprising neural stem cells attached to microcarriers.
- the neural stem cells may, for example, be expanded using the methods of the first aspect of the invention or produced by differentiating ES cells according to the second or third aspect.
- the composition comprises at least 10 8 , 5 x 10 8 , 10 9 or 10 10 cells.
- a further aspect of the invention provides a kit comprising a population of stem cells or the differentiated progeny thereof attached to microcarriers and medium for the maintenance of the cells in culture.
- the cells may be supplied as actively growing cultures or may be frozen using conventional cryopreservation techniques.
- the cells may be supplied in any convenient format for further culture or other applications, including cells in vials, tissue culture plates, flasks or other suitable containers. In one embodiment, the cells are dispensed into multi-well plates ready for use in assays as described herein.
- a further aspect of the invention provides a pharmaceutical composition comprising a population of stem cells or the differentiated progeny thereof attached to microcarriers.
- the microcarriers used in this aspect of the invention are biocompatible and/or biodegradable. It is also desirable, in terms of obtaining regulatory approval, for the composition to be free of animal-derived components. Thus, for example gelatin microparticles and gelatin or collagen coatings are preferably avoided.
- the cells produced according to the methods of the invention are particularly suitable for use in assays, e.g. in drug discovery applications.
- another aspect of the invention provides an assay reagent comprising a population of stem cells or the differentiated progeny thereof attached to microparticles.
- a related aspect of the invention provides use of a population of stem cells or the differentiated progeny thereof attached to microcarriers in an assay for identifying factors that influence cell growth, survival and/or differentiation.
- the factors can be, for example, small molecules including new chemical entities, biological molecules including nucleic acids and proteins, or interactions between one or more molecules. Such interactions may, for example, involve molecular signalling processes that control proliferation, survival and/or differentiation, including ligand-receptor interactions.
- the invention provides an assay for identifying factors that influence cell growth, survival and/or differentiation comprising the steps of:
- a further aspect of the invention provides a method for producing a structured population of stem cells or the differentiated progeny thereof comprising: a) inoculating a first volume of culture medium containing one or more three dimensional substratum supports with stem cells; b) allowing the stem cells to adhere to the one or more substratum supports; and c) incubating the culture under conditions conducive to the proliferation and/or differentiation of the stem cells
- the method comprises adding a second volume of medium to the culture after step b).
- substratum supports have been described, for example in Xu and Reid (2001) Ann NY Acad Sci 944: 144-159.
- the substratum supports are biocompatible and/or biodegradable.
- Such structured populations of cells have potential application, for example in the development of implants for production of insulin.
- the passaging technique and cell harvest were designed for maintenance of cell number, viability and function, in order to produce large numbers of high quality cells.
- the protocols below detail microcarrier culture of mES cells and their harvest in either serum containing or serum free media (ESGRO Complete) and neural differentiation of mES in serum free media (RHB-A®) on microcarriers.
- microcarriers weigh out the required amount of microcarriers and autoclave according to manufacturers instructions. If required microcarriers can be coated by immersion in sterile 0.1% gelatin solution prior to use.
- Typical inoculation cell concentration is 5 x 10 4 cells/ml final culture volume.
- Microcarrier density is dependent on carrier used. For Cultispher gelatin (Percell Biolytica) microcarriers 0.5 - 1g/litre final culture volume is typical. 7. Rinse the spinner flask with media to remove any residual liquid from autoclaving.
- microcarriers such as Cultispher
- suitable enzyme e.g. 0.1% trypsin solution
- spin gently Cells should begin to detach within 2-3 minutes. If using a gelatin microcarrier, such as Cultispher, then continue until microcarriers dissolve completely.
- Cells can be replated and a high proportion of the live cell population is Sox-1 positive.
- microcarriers weigh out the required amount of microcarriers and autoclave according to manufacturers instructions. If required microcarriers can be coated by immersion in sterile 0.1% gelatin solution prior to use.
- microcarriers 0.5 - 1g/litre final culture volume is typical.
- suitable microcarriers include Cytodex1/3 (Amersham Biosciences) used at 1g/litre. 7. Rinse the spinner flask with media to remove any residual liquid from autoclaving. 8. Add the microcarriers and the cell suspension to the stirrer flask. Add sufficient volume of RHB-A® culture media + growth factors so that there is a 1 cm depth of media in the bottom of the spinner flask. Place on spinner base in an incubator at 37 0 C and 7% CO2, with the side caps loosened/ adapted with air filters to allow for gas exchange. Allow the carriers and cells to settle, but gently agitate/spin the flask every two hours to evenly distribute the cells on the carriers.
- CeII growth can be monitored by taking samples from the spinner flask and removing the cells using enzyme. The cells can then be counted.
- Typical yield is in the range of 1-2 x 10 6 cells/ml final culture volume.
- mNS cells can be differentiated on microcarriers by removal of growth factors from the cell culture media.
- Neural cells are optionally removed from the microcarriers. The more differentiated the cells are the more fragile they become, and it may not be possible to remove the cells from the microcarriers using enzymatic methods.
- Example 4 Microcarrier Culture of Human Embryonic Stem (hES) Cells As some hES cells are dependent on feeder cells, this protocol describes a method for co-culture of the hES cells on microcarriers with feeder cells.
- Method 1 Expansion of feeder cells on microcarriers; feeder cells inactivated in situ:
- microcarriers weigh out the required amount of microcarriers and autoclave according to manufacturers instructions. If required microcarriers can be coated by immersion in sterile 0.1% gelatin solution prior to use.
- CeII expansion can be monitored by taking a small sample from the spinner and staining with a nuclear stain such as Hoechst to visualise the cell coverage on the microcarrier.
- feeder cells are deemed to have reached confluence, inactivate by ⁇ -irradiation or mitomycin c treatment.
- Stirring speed may need to be increased over the duration of the culture period as the microcarriers have a tendency to form clumps.
- CeIIs can be removed from microcarriers by enzymatic dissociation using collagenase or Accumax/Accutase. The hES cells can then be replated onto fresh feeders or differentiated as required.
- the invention thus provides large scale production of stem cells, optionally on carriers.
Abstract
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EP08718574A EP2121906A1 (en) | 2007-02-19 | 2008-02-19 | Large scale production of stem cells |
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KR20130131363A (en) | 2010-11-09 | 2013-12-03 | 론차 콜로그네 게엠베하 | Method for controlling binding of cells to a substrate |
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Also Published As
Publication number | Publication date |
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GB0706917D0 (en) | 2007-05-16 |
EP2121906A1 (en) | 2009-11-25 |
GB0703188D0 (en) | 2007-03-28 |
GB0810344D0 (en) | 2008-07-09 |
US20100093083A1 (en) | 2010-04-15 |
GB2449772A (en) | 2008-12-03 |
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