AU2008229981A1

AU2008229981A1 - Immortalized hepatocytes

Info

Publication number: AU2008229981A1
Application number: AU2008229981A
Authority: AU
Inventors: Ronald A Faris; Jin Liu
Original assignee: Multicell Technologies Inc
Current assignee: Multicell Technologies Inc
Priority date: 2004-10-07
Filing date: 2008-10-16
Publication date: 2008-11-06

Description

AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION Standard Patent Applicant(s): MultiCell Technologies, Inc.

Invention Title: IAMM'ORTALIZED HEPATOCYTES The following statement is a full description of this invention, including the best method for performing it known to me/us: P60371 AU IPat-Set-Fih,,g App6c60o 2008-10-14 doc (M) 00

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-q- 0 0 IMMORTALIZED HEPATOCYTES 00 SRELATED APPLICATIONS C This application claims the benefit of U.S. provisional application serial number 60/510,509, filed on October 10, 2003, which is hereby incorporated in its entirety by reference.

GOVERNMENT GRANTS This invention was made in part with United States government support under grant number 70-NANB7H3070 awarded by Advanced Technology Program of the United States Department of Commerce. The U.S. government has certain rights in this invention.

FIELD OF THE INVENTION This invention relates to novel nontumorigenic virally-immortalized normal human hepatocyte cell lines and to the use of these cell lines for toxicity and metabolism testing of potential therapeutic drugs and chemical entities, for the replication of viruses and for the production of therapeutic plasma proteins.

BACKGROUND OF THE INVENTION Toxicity and Metabolism Testing of Potential Therapeutic Drugs and Chemical Entities Drug-induced liver toxicity is an important clinical problem, and several drugs have been withdrawn from the market because of their ability to cause rare but severe (even lethal) cases of hepatotoxicity. Induction of cytochrome P450 (CYP) and related drug-metabolizing 0 0enzymes (DMEs), including transporters, is a well-recognized cause of clinically significant drug-drug interactions, as well as a cause of loss of efficacy (pharmacokinetic tolerance) or

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auto-induction (the process whereby a drug induces its own hepatic metabolism). During

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drug development, in vitro assays can be used to avoid inducers, and characterize drug-drug interaction potential due to increased drug clearance by the liver. In vitro induction studies 00 traditionally use primary hepatocyte cultures and enzyme activity with selected marker C, compounds.

00 0CYPs are involved in the metabolism of drugs, primarily in the liver. For example, induction of CYP3A gene expression is caused by a variety of marketed drugs including rifampin, phenobarbital, clotrimazole, and dexamethasone and represents the basis for a number of common drug-drug interactions (Meunier et al., Expression and induction of CYPIA1/1A2, CYP2A6 and CYP3A4 in primary cultures of human hepatocytes: a follow-up, Xenobiotica 30(6): 589-607, 2000; Sahi et al., Effect of troglitazone on cytochrome P450 enzymes in primary cultures of human and rat hepatocytes, Xenobiotica 30(3): 273- 284, 2000; Luo et al., CYP3A4 induction by drugs: correlation between a pregnane X receptor reporter gene assay and CYP3A4 expression in human hepatocytes, Drug Metab.

Dispos. 30(7): 795-804, 2002; Madan et al., Effects ofprototypical microsomal enzyme inducers on cytochrome P450 expression in cultured human hepatocytes, Drug Metab.

Dispos. 31(4): 421-431, 2003).

Guidelines for assessing enzyme induction in vitro have been outlined in Tucker et al.

(Optimizing drug development: Strategies to assess drug metabolism/transporter interaction potential- toward a consensus, Pharmaceutic. Res. 18: 1071-1080, 2001) and Bjorsson et al.

(The conduct of in vitro and in vivo drug-drug interaction studies: A PhRMA perspective, J.

Clin. Pharmacol. 43: 443-469, 2003). These two "consensus reports" identify primary cultures of human hepatocytes as the method of choice the gold standard for assessing the O0 0enzyme-inducing potential of chemical entities and drug candidates. This in vitro approach, based on a human-derived test system, is superior to an in vivo approach based on tests in

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laboratory animals because drugs are known to cause enzyme induction in a species-specific manner. For example, the two prototypical inducers, namely omeprazole and rifampin, are efficacious inducers of human CYP1A2 and CYP3A4 and yet they do not induce the 00 corresponding enzymes in rats or mice.

,1 Human hepatocytes play several key roles in preclinical drug development. They can 00 0be used to assess the effects of drug candidates on the liver in a clinically meaningful manner the induction and cellular toxicity) and, conversely, they can be used to assess the effects of the liver on chemical entities drug metabolism and species comparisons).

Primary cultures of human hepatocytes have the distinct advantage of exhibiting speciesspecific induction of CYP isoforms; however, the utility of cryopreserved or plated primary human hepatocytes is restricted by the limited and erratic supply of human liver and by significant inter-individual differences in the expression of DMEs and responses to toxicants.

Cell lines of tumorigenic origin, such as HepG2 and H4IIE, are routinely used for comparison of the in vitro toxicity of candidate compounds. Such cells are unlikely to retain many or most of the factors that predict cell-specific toxicity in vivo. For instance, most tumor-derived cells are not highly differentiated; they rapidly proliferate in culture, which requires enormous energy (ATP consumption) and which may increase their sensitivity to cellular insult compared to non-proliferative cells.

Thus, there is a need for a nontumorigenic immortalized human hepatocyte cell line that retains the properties of a normal human hepatocyte, namely metabolic and transporter function, while offering the distinct advantages of reproducibility and unlimited availability.

Therapeutic Plasma Proteins 00 There is a great demand for therapeutic plasma proteins (TPPs), such as albumin, a-i antitrypsin (AAT), blood clotting factors VIII and IX, and inter-a-inhibitor proteins (laIp).

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C The production of TPPs by cell-based systems would avoid the hazards of blood-derived products, such as potential contamination with viruses or other pathogens.

SCurrently, the majority of proteins that have been approved for clinical and 00 Stherapeutic use are mass-produced by recombinant protein technology. Although these c products have been proven safe and effective, not all behave identically to their native 00 0counterparts. For example, recombinant factors (rF) VIII and IX are more rapidly cleared following infusion than their plasma derived counterparts. Shapiro, E. Bemtorp, and M.

Morfini, Incremental recovery assessment and effects ofweight and age in previously untreated patients treated with recombinantfactor IX. Blood, 2000. 96 (suppl p. 265a.

Recent findings suggest that this is the result of incomplete or inappropriate post-translational modification.

Hemophilia A (Factor VIII deficiency) occurs in 1 in 5, 000 to10, 000 males in the United States. In contrast, the incidence of hemophilia B (Factor IX deficiency) is 0.25 in 10,000 males.

Currently, plasma-derived and recombinant Factor VIII and IX concentrates are used for the lifetime treatment of hemophilia. It is estimated that three-quarters of the worldwide hemophilia population receive little or no treatment due to a shortage of these TPPs. Thus, there is a clear need for fully functional, fully native blood-clotting factors that overcome the shortcomings of recombinant or blood-derived TPPs.

a-1-antitrypsin (AAT) is a human blood protein. Severe AAT deficiency (hereditary emphysema) is thought to affect around 150,000-200,000 individuals in Europe and the United States. Many respiratory diseases including AAT congenital deficiency, cystic fibrosis and chronic obstructive pulmonary disease are characterized by an imbalance of AAT and elastase in the lung. Administration of supplemental AAT is clinically effective at 0 0alleviating the deleterious effects to the lung that occur in these diseases.

Currently, there is only one plasma-derived AAT licensed in the United States, which has been in very limited supply. Thus, there is a clear need for a fully functional, fully native AAT that can overcome the shortcomings of recombinant or blood-derived TPPs.

Sepsis, a disease characterized by an overwhelming systemic response to infection, can strike 00 anyone and can be triggered by events such as pneumonia, trauma, surgery and bums, or by C1 conditions such as cancer or AIDS. In the United States, sepsis is the leading cause of death in the 00 Snoncardiac intensive care unit and the 11 th leading cause of death overall. Currently, treatment for sepsis is limited to attempts to manage the underlying infection and supportive therapy if the infection leads to organ dysfunction. Despite intensive medical care, up to 50% of patients still die from this illness.

Inter-a-inhibitor proteins (lalp) are natural serine protease inhibitors found in relatively high concentration in plasma that play roles in inflammation, wound healing and cancer metastasis. Bost, M. Diarra-Mehrpour, and J.P. Martin, Inter-alpha-trypsin inhibitor proteoglycan family-a group ofproteins binding and stabilizing the extracellular matrix. Eur J Biochem, 1998. 252: p. 339-346. Ialp is believed to have a predictive value in septic patients. Lim, et al., Inter-trypsin inhibitor: decreased plasma levels in septic patients and its beneficial effects in an experimental sepsis model. Shock, 2000. 13 (Suppl.): p. 161. In-vivo animal studies using a sepsis rat model have shown that administration of Ialp dramatically improved survival rates. Yang S, et al., Administration of human interalpha-inhibitors maintains hemodynamic stability and improves survival during sepsis. Crit Care Med. 2002 Mar; 30(3):617-22. The results strongly support the therapeutic potential of Ialp in the management of severe sepsis. Yet, there is no ready supply of Ialp for administration to septic patients. Thus, there is a clear need for fully functional, fully native 00 Icalp to overcome the shortcomings of recombinant or blood-derived TPPs.

There are a number of patents and publications that describe immortalized cell lines: U.S.

Patent No. 6,107,043 (Jauregui); U.S. Patent No. 5,665,589 (Harris); U.S. Patent App. No.

2002/0045262 Al (Prachumsri); and International publication No. WO 99/55853 (Namba).

However, to date, among other things, the prior art cell lines do not provide a means to safely, 00 Seffectively, and cost efficiently perform the protein post-translational modifications, such as C glycosylation, that are critical in the production of functional therapeutic plasma proteins; produce 00 Ssimultaneously multiple therapeutic plasma proteins, especially factor VIII protein or factor IX; and maintain the continuous expression of active levels of cytochrome P450 enzyme in a serum-free media. Thus there is a need for a nontumorigenic immortalized human hepatocyte cell line that retains the properties of a normal human hepatocyte, and can be used to produce properly processed therapeutic plasma proteins.

SUMMARY OF THE INVENTION The present invention relates to nontumorigenic, virally-immortalized human hepatocyte cell lines, that can be maintained in serum-free media, and produce endogenous plasma proteins, such as albumin, ac-1 antitrypsin, blood clotting factors VIII and IX, and inter-a-inhibitor proteins (IaIp). In a preferred embodiment, the nontumorigenic, immortalized cell lines comprise the Fa2N-4 (ATCC Accession Number 5566) and EalC-35 (ATCC Accession Number 5565) cell lines deposited under the terms of the Budapest Treaty at the American Type Culture Collection (ATCC), 12301 Parklawn Drive, Rockville, Md., on October 6, 2003.

In a preferred embodiment of the present invention, the cell lines are derived from normal hepatocytes. Preferably, the cell lines are derived from normal human hepatocytes.

More preferably, the cell lines are derived from cryopreserved normal human primary hepatocytes.

In another preferred embodiment of the present invention, the cell lines proliferate 00 easily in media. Preferably, the cell lines proliferate easily in a serum-free media. More Spreferably, the cell lines proliferate easily in MFE media (MultiCell Technologies Inc., Providence, RI, USA; XenoTech, LLC, Lenexa, KS, USA).

In another preferred embodiment of the present invention, the cell lines contain a substantially pure SV40 DNA. Preferably, the SV40 DNA encodes the wild type SV40 large 00 T and small t antigens (TAg). More preferably, the DNA encodes the wild type TAg and ,I does not encode other SV40 gene products.

00 In another preferred embodiment of the present invention, the cell lines retain their hepatic functions in a serum-free media. Preferably, hepatic functions are the ability to continue to express enzymatic activity and produce proteins. More preferably, hepatic functions include the ability to continue to maintain cytochrome P450 (CYP) enzymatic activities and produce fully-functional therapeutic plasma proteins (TPPs) in a serum-free media.

In another preferred embodiment of the present invention, the cell lines can be used to assess the effects of drug candidates on the liver. Preferably, the cell lines will be used to assess enzyme induction and cellular toxicity.

In another preferred embodiment of the present invention, the cell lines can be used to assess the effects of the liver on chemical entities. Preferably, the cell lines will be used to assess drug metabolism and species comparisons.

In another preferred embodiment of the present invention, the cell lines continue to produce proteins. Preferably, the cell lines continue to naturally produce plasma proteins.

More preferably, the cell lines continue to naturally produce TPPs comprising albumin, a-1antitrypsin, blood clotting factors VIII and IX, transferrin and inter-a-inhibitor proteins (Ialp).

In another preferred embodiment of the present invention, production of TPPs by the 00 cell lines is measured. Preferably, production of TPPs by the cell lines is measured by Sdetecting their presence in the serum-free media. More preferably, production of TPPs by the

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cell lines is measured at the protein level rather than at the mRNA level.

In another preferred embodiment of the present invention, the cell lines produce TPPs in serum-free media. Preferably, the cell lines simultaneously produce TPPs out of the same 00 fraction in serum-free media. More preferably, the cell lines simultaneously produce TPPs N out of the same fraction in serum-free media without the reoccurring risk of viral 00 contamination.

BRIEF DESCRIPTION OF THE DRAWINGS Figures 1 through 8 show the RT-PCR products for the expression analysis of several mRNA transcripts in EalC-35 and Fa2N-4 cells. The legend for the gel loading order is outlined in Tables 1 and 2 below.

Figure 9a shows immunostaining of the EalC-35 immortalized hepatocyte cell line for large T antigen that confirms the integration of SV40DNA into genomic DNA of the immortalized cell.

Figure 9b shows immunostaining of cultured Fa2N-4 cells that demonstrates that the proliferating cells continue to express albumin.

Figure 9c shows the morphology of the immortalized cells with well-defined nucleoli and granulated cytoplasm, which are characteristic features of normal primary hepatocytes.

Figure 10 shows the inducibility of testosterone metabolism after treating Fa2N-4 cells with different CYP3A4 inducers.

Figure 11 shows an immunoblot demonstrating the induction of CYP3A4 consequent of treatment of Fa2N-4 and EalC-35 with Rifampin (RIF), beta-naphtoflavone (BNF) and 0 phenobarbital C is the untreated control. It should be noted that the upper band is 0 Snonspecific and that BNF, a CYP1A inducer, does not induce CYP3A4 protein expression.

Figure 12 shows the morphology of human hepatocytes (upper) and Fa2N-4 cells

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C (lower) at the light microscopy level. Note that Fa2N-4 cells look remarkably similar to human hepatocytes.

Figure 13 shows induction of CYP enzymes by omeprazole and rifampin in Fa2N-4 00 Scells, cultured in 6-well plates.

Figure 14 shows the reproducibility of CYP2B6 induction in rifampin-treated Fa2N-4 00 0cells.

Figure 15 shows reproducibility of CYP enzyme induction in Fa2N-4 cells across several passages. Dotted lines represent median fold induction in fresh human hepatocytes.

Figure 16 shows the effect of cell culture format on induction of CYP2B6 in Fa2N-4 cells.

Figure 17 shows the effect of cell culture format 12-, 24-, or 96- well plate) on CYP1A2 and CYP3A4 induction in Fa2N-4 cells.

Figure 18 shows a time course of CYPIA2 and CYP3A4 induction in Fa2N-4 cells.

Figure 19 shows concentration-response curves for CYPIA2 and CYP3A4 induction in Fa2N-4 cells.

Figure 20 shows the effect of various enzyme inducers on CYP1A2 and CYP3A4 activity in Fa2N-4 cells.

Figure 21 shows the range of CYP3A4 induction in primary cultures of human hepatocytes. Note the difference between the median and mean induction value.

Figure 22 shows the utility of Fa2N-4 cells in differentiating toxicants from nontoxicants by measuring the release of a-GST into media following 72-hour exposure to compounds.

Figure 23 shows the dose-response dependence of CYP3A4 induction by rifampin in O Fa2N-4 cells. Measurement of induction of CYP3A4 was performed in Fa2N-4 cells treated with 100 nM to 50 pM rifampin. Data was fitted using SigmaPlot (version 8) using a 3-

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parameter sigmoidal curve. Total RNA was analyzed to determine the level of CYP3A4 transcript and then compared to vehicle control to determine fold-induction. Data represents mean SD from the data of triplicate samples. CYP3A4 activity was measured by 00 formation of the testosterone metabolite 6 -beta-hydroxytestosterone and then compared to N vehicle control to determine fold-induction. Data represents mean SD from the data of 00 triplicate samples.

Figure 24 shows induction of CYP3A4 in different passages of Fa2N-4 cells. Various passages of Fa2N-4 cells were plated in 24-well plates and exposed to 0.1% DMSO vehicle (open bars), 50 gM dexamethasone (striped bars), and 10 pM rifampin (black bars). The levels of CYP3A4 transcripts were quantified from isolated total RNA. Plot represents the mean SD from the data of quadruplicate samples. CYP3A4 activity was measured by formation of the testosterone metabolite 6 -beta-hydroxytestosterone. Plot represents the mean of duplicate samples. All compounds showed statistically significant increase in transcript versus vehicle control treatment (Student's t-Test, p<0.05).

Figure 25 shows the comparison of CYP3A4 induction in various multiwell plate formats. Induction of CYP3A4 transcript in Fa2N-4 cells after 48 hour exposure to 10 piM rifampin (closed bars) in comparison with vehicle (open bars). Data is from studies conducted in each multiwell plate format as indicated. Plot represents the mean SD from the data of quadruplicate samples. All compounds showed statistically significant increase in transcript versus vehicle control treatment (Student's t-Test, p<0.05).

Figure 26 shows the following lanes: 1) Human Plasma; 2) Protein Marker Line; 3) Culture Medium (Control); 4) Primary human hepatocytes (72 hr culture); 5) monolayer, 72 hrs culture; 6) EalC-35, roller bottle, 7-day culture; 7) EalC-35 roller bottle

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0/14-day culture; 8) Fa2N-4 monolayer /72 hrs culture; 9) Fa2N-4 roller bottle /7-day culture; Fa2N-4, roller bottle /14-day culture.

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Figure 27 shows an immunoblot using an anti-transferrin antibody with the following lanes: 1) Marker; 2) EalC-35p15; 3) EalC-35p24; 4) EalC-35p29; 5) EalC-35 p43; 6) Fa2N-4p10; 7) Fa2N-4-p23; 8) Fa2N-4p31; 9) Fa2N-4p39; 10) Human Plasma.

00 Figure 28 shows two-dimensional gel analysis of secreted proteins of the Fa2N-4 and ,l EalC-35 cell lines and western blot analysis of the EalC-35 gel with anti-Factor-IX antibody.

00 SFigure 29 shows the expression of plasma proteins albumin, Ialp, and AAT in Fa2N- 4 cells grown in T25, T75, and T 50 flasks.

Figure 30 shows total albumin secretion by Fa2N-4 cells after three and six days in culture in T25, T75, and T150 flasks.

Figure 31 shows a photograph of the ELISA plate 1 containing a colorimetric enzyme immunoassay for the quantitative determination of secreted hGH utilizing the sandwich ELISA principle. The key for this plate is shown below in Table 13.

Figure 32 shows a photograph of the ELISA plate 2 containing a colorimetric enzyme immunoassay for the quantitative determination of secreted hGH utilizing the sandwich ELISA principle. The key for this plate is shown below in Table 13.

Figure 33 shows a photomicrograph of Fa2N-4 cells immunstained for CD81. Note that expression of CD81 is localized to the plasma membrane.

DETAILED DESCRIPTION OF THE INVENTION 00 C, Abbreviations and Terms O In accordance with the present invention and as used herein, the following terms and abbreviations are defined with the following meanings, unless explicitly stated otherwise.

These explanations are intended to be exemplary only. They are not intended to limit the 00 terms as they are described or referred to throughout the specification. Rather, these explanations are meant to include any additional aspects and/or examples of the terms as 00 described and claimed herein.

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C The following abbreviations are used herein: AAT c-1l-antitrypsin DME drug metabolizing enzyme IcaIp inter-alpha-inhibitor proteins MCT MultiCell Technologies MFE Multi-Functional Enhancing media RT-PCR reverse transcription polymerase chain reaction Simian Virus TAg Simian Virus 40 T antigen and t antigen tAg Simian Virus 40 t antigen TPP therapeutic plasma protein The term "cell line" refers to a population or mixture of cells of common origin growing together after several passages in vitro. By growing together in the same medium and culture conditions, the cells of the cell line share the characteristics of generally similar growth rates, temperature, gas phase, nutritional and surface requirements. The presence of cells in the cell line expressing certain substances, for example albumin, can be ascertained, provided a sufficient proportion, if not all, of the cells in the line produce a measurable 00 quantity of the substance. An enriched cell line is one in which cells having a certain trait, e.g. expressing albumin, are present in greater proportion after one or more subculture steps, than the original cell line.

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The term "clonal cells" are those, which are descended from a single cell. As a

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practical matter, it is difficult to obtain pure cloned cell cultures of mammalian cells. A high degree of cell purity can be obtained by successive rounds of cell enrichment. As used herein, 00 N a cell culture in which at least 80% of the cells possess a defined set of traits is termed a

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C1 cloned cell culture. Preferably, a cell culture in which at least 90% of the cells possess a 00 defined set of traits is termed a cloned cell culture. More preferably, a cell culture in which at least 98% of the cells possess a defined set of traits is termed a cloned cell culture. The Fa2N-4 and EalC-35 cell lines claimed in this invention are clonal cell lines.

The term "immortalization" is defined as the acquisition of an indefinite proliferative capacity. Immortalization may be induced in primary cultured cells and finite cell lines by tranfection with telomerase, oncogenes, or the large T antigen of the SV40, or by infection with SV40. Immortalization is not necessarily a malignant transformation, though it may be a component of malignant transformation.

The term "immortalized" refers to the cell line that grows continually without senescence when cultured in vitro in a suitable growth medium.

The term "virally-immortalized" refers to hepatocytes being transfected or infected with all or part of the viral genome of a wild type or mutant virus. Preferably, the virus is a DNA virus. More preferably, the virus is SV40, which binds to p53 and Rb tumor suppressor proteins, leading to inactivation of their tumor suppressor pathways.

The term "substantially pure" refers to a DNA which has been purified from the sequences which flank it in a naturally occurring state, a DNA fragment which has been removed from the sequences which are normally adjacent to the fragment, the sequences adjacent to the fragment in the genome in which it naturally occurs, and which has been 00 Ssubstantially purified from other components which naturally accompany the DNA, e.g., DNA which has been purified from the proteins which naturally accompany it in the cell.

O The term "hepatocytes" refers to liver cells that are capable of considerable

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regeneration in response to loss of liver mass through hepatotoxic processes, disease, or surgery), and constitute about 80% of the cell population of the liver. They are large 00 polygonal cells measuring between 20-30 pm. Hepatocytes have as many as 200-300 Nperoxisomes per cells, which are involved in the breakdown of hydrogen peroxide, produced 00 in many of the general cytoplasmic metabolic activities. In addition, peroxisomes have specific oxidative functions in gluconeogenesis, metabolism of purines, alcohol and lipids.

The smooth endoplasmic reticulum (sER) in hepatocytes contain enzymes involved in degradation and conjugation of toxins and drugs. Under conditions of hepatocyte challenge by drugs, toxins or metabolic stimulants, the sER may become the predominant organelle in the cells. Hepatocytes perform multiple finely-tuned functions which are critical to homeostasis. Of the variety of cell types in the mammalian body, only hepatocytes combine pathways for synthesis and breakdown of carbohydrates, lipids, amino acids, protein, nucleic acids and co-enzymes simultaneously to accomplish a unique biological task.

The term "isolated hepatocyte" refers to a hepatocyte that has been physically separated from other cells to which it is attached in its natural environment.

The term "primary hepatocyte" refers to a hepatocyte that has been recently isolated from intact liver tissue.

The term "normal primary human hepatocyte" refers to a hepatocyte derived from a nondiseased human liver and maintained in vitro for a finite period when cultured in a suitable medium.

The term "cryopreserved human hepatocyte" refers to a normal primary human 0 0hepatocyte that was cryopreserved prior to being cultured in a suitable medium.

The term "metabolic activity" refers to the sum total of the chemical reactions that

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proceed in a cell, including catabolism (breaking down) and anabolism (building up). The metabolic activity in a hepatocyte includes, but is not limited to, the ability to process potentially toxic compounds, a drug or endogenous metabolite, into a less toxic or non- 00 toxic compound.

N The term "cytochrome P450 enzyme" or "CYP" refers to a family of heme-based 00 Soxidase enzymes found predominantly in the liver. These enzymes form the first line of defense against toxins and they are involved in the metabolism of hydrophobic drugs, carcinogens, and other potentially toxic compounds and metabolites circulating in the blood.

They are found tethered to the surface of the endoplasmic reticulum, where they attach a chemical handle onto carbon-rich toxins. Then, other enzymes may further modify the compound, making the entire molecule more water soluble. This allows the toxins to be eliminated by the urinary and digestive systems. The CYP family is divided into subfamilies, which include, but are not limited to, CYP1A, CYP2A, CYP2C, CYP2D, CYP2E, and CYP3A. Within these subfamilies there are numerous human CYP enzymes, often termed "isozymes" or "isoforms." The human CYP3A, CYP2D6, CYP2C, and CYP1A isoforms are known to be important in drug metabolism. See, Murray, 23 Clin. Pharmacokinetics 132-46 (1992). CYP3A4 is by far the major isoform in human liver and the small intestines, comprising 30% and 70% respectively of the total CYP450 protein in those tissues. Based primarily on in vitro studies, it has been estimated that the metabolism of 40% to 50% of all drugs used in humans involve CYP3A4 catalyzed oxidations. See Thummel, K. E. Wilkinson, G. In Vitro and In Vivo Drug Interactions Involving Human CYP 3A, 38 Ann.

Rev. Pharmacol. Toxicol., 389-430 (1998).

The term "hepatic function" refers to liver specific biological functions, which 00 include, but are not limited to, gluconeogenesis; glycogen synthesis, storage, and breakdown; synthesis of serum proteins including, but not limited to, albumin, C hemopexin, ceruloplasmin, the blood clotting factors (including, but not limited to, Factors V, VII, VIII, IX, X, prothrombin, and fibrinogen), alpha 1--antitrypsin, transferrin, and antithrombin III,; conjugation of bile acids; conversion ofheme to bile pigments; (6) 00 Slipoprotein synthesis; vitamin storage and metabolism; cholesterol synthesis; (9) ammonia metabolism, including urea synthesis and glutamine synthesis; (10) amino acid 00 metabolism, including metabolic conversion and re-utilization of aromatic amino acids; and (11) detoxification and drug metabolism.

Immortalized Human Hepatocvte Cell Lines This invention relates to virally-immortalized hepatocyte cell lines, which may be derived from normal primary human liver cells, have the ability to proliferate in a serum-free media, are nontumorigenic, and are capable of producing endogenous plasma proteins, such as albumin, a-I antitrypsin, blood clotting factors VIII and IX, transferrin and inter-a-inhibitor proteins (Ialp) but do not express alpha-fetoprotein when measured at the protein level. In a preferred embodiment, the nontumorigenic, immortalized cell lines comprise the Fa2N-4 (ATCC PTA-5566) and (ATCC PTA-5565) cell lines deposited under the terms of the Budapest Treaty at the American Type Culture Collection, 12301 Parklawn Dr., Rockville, Md., on October 6, 2003.

In another preferred embodiment of the present invention, the cell lines proliferate easily in media. Preferably, the cell lines proliferate easily in a serum-free media. More preferably, the cell lines proliferate easily in MFE media (MultiCell Technologies Inc.,

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0Providence, RI, USA; XenoTech, LLC, Lenexa, KS, USA).

In another preferred embodiment of the present invention, the cell lines contain a

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substantially pure SV40 DNA. Preferably, the SV40 DNA encodes the wild type SV40 large T and small t antigens (TAg). More preferably, the DNA encodes the wild type TAg and does not encode other SV40 gene products.

00 The inventors have developed a large number of proprietary immortalized human C hepatocyte cell lines. The majority of these cell lines were created using SV40 TAg as the 00 immortalization gene. This strategy was chosen because transfection of human cells with SV40 TAg can result in cell lifespan extension and in nontumorigenic immortalization since the cells are semipermissive to viral infection. Cascio, Novel strategies for immortalization of human hepatocytes. Artificial Orgs, 2001. 25: p. 529-538.

Often SV40 TAg immortalized cell lines retain varying levels of the differentiated characteristics associated with the primary cell type and do not display tumorigenicity prior to extensive passage in vitro. Kuroki, T. and N. Huh, Why are human cells resistant to malignant cell transformation in vitro? Jpn J Cancer Res, 1993. 84: p. 1091-1100.

The normal human liver primary cells can be made to grow continuously by transfecting the cells with the SV40 TAg gene. Transfection or infection can be accomplished by use of a virus or a plasmid containing the SV40 TAg gene, and may lead to transformation of the cell line. Other transformation vectors may also be useful, such as papilloma virus or Epstein Barr virus. The techniques for making continuous human cell lines are described in the following references: Grahm. F. Smiley Russell, W. C. and Naim, R.

Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J.

Gen. Virol., 36:59-72 (1977); Zur Hausen, H. Oncogenic herpes viruses In: J. Tooze DNA tumor viruses, Rev. Ed. 2, pp 747-798. Cold Spring Harbor, Cold Spring Harbor Press (1981); Popovic, Lange-Wantein, Sarin, P. Mann, D. and Gallo, R. C.

00 Transformation of a human umbilical cord blood T-cells by human T-cell leukemia/lymphon virus (HTLV), Proc. Natl. Acad. Sci. USA 80:5402-5406 (1983); DiPaolo, J. A. Pirisi, I.,

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Popeseu, N. Yasumoto, Poniger, J. Progressive changes induced in human and mouse

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cells by human Papillomavirus Type-16 DNA, Cancer Cells 5:253-257 (1987).

Digestion of donor, human liver was performed in vitro with pre-perfusion of oxygen- 00 saturated, calcium-free buffer at 37 0 C. Pre-perfusion continued until the liver was blanched and followed by perfusion with oxygen-saturated, collagenase buffer until the liver was 00 thoroughly digested (approximately 45 minutes).

To harvest cells, the liver was minced into 1 cm 2 pieces with the resulting suspension filtered through a #10 wire screen, then filtered again through a 253 tm nylon mesh. The suspension was centrifuged at 20 x g for five minutes at 4 0 C to sediment intact parenchymal cells. The pellet was resuspended at 4 0 C and washed with washing buffer (3X) to remove all collagenase. The cell pellet was resuspended in 150ml tissue culture media to yield a final volume of 400-500ml with a density of 3-4x10 7 cells/ml. Trypan blue and lactate dehydrogenase viability assessment was performed on aliquots of this suspension.

The freshly isolated human hepatocytes isolated from donor liver as described above were washed with washing buffer three times by centrifuging at 50 x g for 5 minutes. The cell pellet was resuspended in chilled freezing medium (serum-free MFE medium: FBS:DMSO at a final cell density of 5x 10 6 /ml. Aliquots of the cell suspension were transferred to Nunc Cryovials (1.0 ml/1.5ml cryovial, 4.5ml/5 ml cryovial). The cells in cryovials were equilibrated at 4 0 C for 15-30 minutes, and the cryovials were then placed in a styrofoam container at -80 0 C for at least 3 hours. The vials were then plunged in liquid nitrogen for storage.

Cyropreserved human hepatocytes were rapidly thawed in a 42°C water bath, washed and 0 0plated in MCT's proprietary MFE culture medium. Two days later the immortalizing gene was introduced into the cells by lipofection-mediated transfection.

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The EalC-35 cell line (ATCC PTA-5565) was derived from transfection with an immortalization vector containing the 2.5kb early region of the SV40 genome, which encompasses both the large-T and small-t antigens, and whose expression is driven by the SV40 early promoter.

00 This early region was inserted into the Stratagene pBluescript SK vector backbone and was named C1 pBlueTag. Neomycin resistance was conferred on the transfected cells as a selectable marker by co- 00 transfection of a neo plasmid. Clones were initially selected based on their ability to grow in G418 containing media. The Eal C-35 cell line was established and maintained in CSM medium.

The Fa2N-4 cell line (ATCC PTA-5566) was immortalized via lipofection-mediated transfection with a single immortalization vector. The early region of the SV40 genome, contained in the pBlueTag vector, was inserted into a backbone based upon the InvivoGen pGT60mcs plasmid and was named pTag-1. The SV40 TAg coding region is under the influence of a hybrid hEFI HTLV promoter. The vector also encodes a hygromycin resistance gene as a drug selectable marker.

Clones were selected based on their ability to grow in hygro containing media. The Fa2N-4 cell line was established and maintained in MFE.

The Fa2N-4 (ATCC PTA-5566) and EalC-35 (ATCC PTA-5565) cell lines were deposited under the terms of the Budapest Treaty at the American Type Culture Collection, 12301 Parklawn Dr., Rockville, Md., on October 6, 2003.

Both the Fa2N-4 (ATCC PTA-5566) and EalC-35 (ATCC PTA-5565) cell lines have been maintained in culture for up to 18 months through 150 population doublings. Both of these cell lines went through a crisis stage between passages 15-20. The immortalized cell lines that emerged grow and function when maintained in MCT's proprietary MFE media without serum and can be cryopreserved indefinitely without detriment. The cell lines will also grow and function in other serum free media. The EalC-35 cell line will also grow and O0 function in media with serum. The cell lines have a doubling time of 72-96 hours. Results from nude mice transplantation studies have indicated that both the Fa2N-4 (ATCC PTA-

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5566) and EalC-35 (ATCC PTA-5565) cell lines are non-tumorigenic.

Toxicity and Metabolism Testing of Potential Therapeutic Drugs and Chemical Entities In another preferred embodiment of the present invention, the cell lines retain hepatic 00 function in a serum-free media. Preferably, hepatic function is the ability to continue to CN express enzymatic activity. More preferably, hepatic function includes the ability to continue 00 Sto maintain cytochrome P450 (CYP) enzymatic activities and other drug metabolizing enzymes (DMEs) in a serum-free media.

Fa2N-4 (ATCC PTA-5566) and EalC-35 (ATCC PTA-5565) cell lines can be used for enzyme induction studies and to examine compounds for their ability to cause cellular toxicity. CYP1A2 and CYP3A4 activity is inducible in both Fa2N-4 and cells which distinguishes these cell lines from other hepatic cell lines. CYP1A2, CYP2B6, CYP2C9, and CYP3A4 activity is inducible in Fa2N-4, which distinguishes this cell line from the EalC-35 cell line. The immortalized hepatocyte cell lines of this invention express sufficient CYP for enzyme induction to be assessed based on measurements of enzymatic activity, as well as mRNA levels. Furthermore, the cell lines of this present invention have been shown to conjugate acetaminophen with glucuronic acid and/or sulfate. Thus, the cell 0 lines can be used in assessing the metabolic stability of drug candidates.

Fa2N-4 cells in culture are morphologically and functionally similar to primary

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cultures of human hepatocytes. The response of this cell line to enzyme inducers closely resembles that observed in cultured primary human hepatocytes, which are considered the in vitro system of choice the gold standard for assessing the enzyme-inducing potential of 00 drug candidates. Fa2N-4 cells offer a number of advantages over primary human C1 hepatocytes; some of which make Fa2N-4 cells a promising in vitro test system for higher 00 throughput screening of chemical entities.

In contrast to human liver, the supply of which is limited and erratic, Fa2N-4 cells are available in unlimited supply. Since accessibility to fresh human hepatocytes is reliant on availability of a suitable liver tissue donor, it can take a long time to conduct experiments using hepatocytes isolated from three different livers to verify that a certain compound is an inducer. In addition, plating efficiency of fresh hepatocytes is unpredictable, so it is not uncommon to have a suitable donor, but find that the cells are not usable due to poor plating efficiency or substandard cell health.

Fa2N-4 cells can be passaged and used over several passages while retaining the activity of the major DMEs. With fresh human hepatocytes, cells can only be used one time, making it difficult to compare data between studies. Plateable cryopreserved primary human hepatocytes are an improvement by theoretically allowing multiple experiments at different times from a single donor, or potentially the use of multiple donors at one time. However, plateable cryopreserved primary hepatocytes are in limited supply. Both fresh primary hepatocytes and plateable cryopreserved hepatocytes have donor-to-donor variability, based on the influence of genetics, the environment, and co-medications. There are vast differences seen in the DME profile of donors, leading to the current recommendation of obtaining data from three donors before reaching a conclusion for induction potential of a chemical.

Induction of CYP enzyme activity in Fa2N-4 cells is more reproducible than it is in human hepatocytes. Furthermore, CYP induction in Fa2N-4 cells can be measured in a variety of cell culture formats, including 96-well plates, whereas this is not always possible with human hepatocytes. Thus, the immortalized hepatocytes of this present invention, 00 namely the Fa2N-4 cells, can be a suitable substitute for fresh human hepatocytes in C1 induction studies, and provide the additional attribute of being amenable for higher 00 throughput studies. Fa2N-4 cells are superior to previously published immortal cell lines, as they show induction of a varied number of genes. These cells can be used to determine the induction potential of a drug, with findings consistent with monitoring increased enzyme activity in primary human hepatocytes. Higher throughput cell culturing and analysis via mRNA endpoint enables more compounds to be tested and reduces the cost per compound; two favorable traits for drug discovery assays.

The cell lines of the present invention are uniquely suited for many in vitro applications and testings, including, but are not limited to, the following: Identification of potential chemotherapeutic drugs: These cells are useful for screening chemicals suitable for the treatment of cancer and related diseases, by growing them in vitro in medium containing the chemical to be tested and then, after a suitable period of exposure, determining whether and to what extent cytotoxicity has occurred, e.g. by trypan blue exclusion assay or related assays (Paterson, Methods Enzymol, 58:141 (1979)), or by growth assays such as colony forming efficiency (MacDonald et al, Exp. Cell. Res., 50:417 (1968)), all of which are standard techniques well known in the art.

Identification of new drug targets. Potential new drug targets can be identified by screening biological and chemical agents for their ability to induce or inhibit genes and metabolic pathways. Chemical and biological substances are screened for their ability to 00 induce or inhibit gene expression or metabolic pathways by adding them to the growth medium of these liver cells and then after a suitable period of time, determine whether a

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,O complex of changes, including cessation of DNA synthesis, induction or inhibition of gene expression (as measured by RT-PCR analysis or genomic expression profiling) and production of liver specific proteins (as determined by immunochemical techniques) occurs.

00 Identification of the effects of chemical and biological substances on the induction or r inhibition of gene expression and metabolic pathways is a way to identify new drug targets 00 for treating diseases such as cancer.

Studies of metabolism of carcinogens and other xenobiotics: Carcinogens and other xenobiotics may be added to the growth medium of these cells and the appearance of metabolic products of these compounds may be monitored by teclhniques such as thin layer chromatography or high performance liquid chromatography and the like, and the interaction of the compounds and/or their metabolites with DNA is determined.

Studies of DNA mutagenesis: Substances known or suspected to be mutagens may be added to the growth medium of the cells and then mutations may be assayed, by detection of the appearance of drug resistant mutant cell colonies (Thompson, Methods Enzymol, 58:308, 1979).

Studies of chromosome damaging agents: Substances known or suspected to cause DNA or chromosomal damage may be added to the culture medium of these cell lines, and then the extent of chromosomal damage may be measured by techniques well known in the art, such as measurement of the frequency of sister chromatic exchange (Latt et al. In: Tice, R. R. and Hollaender, Sister Chromatic Exchanges, New York: Plenum Press, pp, 11 ff.

(1984)). While there is a wealth of methods for differentiating between sister chromatids, a few simple techniques can suffice for most studies. Representative techniques, employing 00 33258 Hoechst fluorescence A. Latt et al., Proc. Natl. Acad. Sci. USA 70:3395 (1973); S.

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SA. Latt et al., Cytochem. 25:913 (1977)) or 33258 Hoechst followed sequentially by illumination, SSC incubation, and Giemsa staining (adapted from P. Perry and S. Wolff,

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NO Nature 261:156 (1974); S. Wolff (1981), Measurement of sister chromatid exchange in mammalian cells. In DNA Repair: A Laboratory Manual of Research Procedures, Vol. 1, Part B C. Friedberg and P. C. Hanawalt, Eds.), Dekker, are just two examples of such 00 techniques that may be used.

Studies of cytotoxicity of drugs, chemical entities, carcinogens, and xenobiotics: SDrugs, chemical entities, carcinogens, and xenobiotics may be added to the growth medium of the cells and the viability of the cells as a function of time of exposure may be ascertained using gene expression profiling, dye exclusion, enzyme leakage, colony forming efficiency, etc. assays.

Studies of gene expression: drugs and chemical entities may be added to the culture medium of the cells and changes in gene expression as a function of exposure may be monitored using RNA and protein expression as biological endpoints. Changes may reflect either induction or inhibition of specific genes. For example, cells may be cultured with drugs and chemical entities to identify those agents that modulate the expression of drug metabolism enzymes including but not limited to CYPs designated CYP3A4 or CYP1A2, the multi drug resistance gene, biliary transporters, glucuronyl transferases, glutathione transferases, sulfatases, etc.

The immortalized cells may be used to identify new drugs to treat hepatitis C virus (HCV) infection. The inventors have shown that both the EA1C-35 cell line and the Fa2N-4 cell line express CD81; CD81 is required for HCV mediated viral infection (Cormier, et al, PNAS, 101:7270-7274, 2004). Cell lines can be infected by culturing the cells with HCV positive sera. Cell lines propagating HCV virus may be used to screen for new drugs to treat this chronic infection.

00 0Therapeutic Plasma Proteins (TPPs) In another preferred embodiment of the present invention, the cell lines continue to Oproduce proteins. Preferably, the cell lines continue to naturally produce plasma proteins.

More preferably, the cell lines continue to naturally produce therapeutic plasma proteins More preferably, the cell lines continue to naturally produce therapeutic plasma proteins (TPPs) comprising albumin, a-1-antitrypsin, blood clotting factors VIII and IX, transferrin 00 and inter-a-inhibitor proteins (Illp).

SIn another preferred embodiment of the present invention, production of TPPs by the Scell lines is measured. Preferably, production of TPPs by the cell lines is measured by detecting their presence in the serum-free media. More preferably, production of TPPs by the cell lines is measured at the protein level rather than at the mRNA level.

In another preferred embodiment of the present invention, the cell lines produce TPPs in serum-free media. Preferably, the cell lines simultaneously produce TPPs out of the same fraction in serum-free media. More preferably, the cell lines simultaneously produce TPPs out of the same fraction in serum-free media without the reoccurring risk of viral contamination.

Hepatocyte-derived proteins provide a safer, more reproducible approach for producing native plasma proteins for therapeutic applications. This finding is based upon Applicant's data that demonstrates its proprietary, immortalized human hepatocyte cell lines, continue to produce inter-ainhibitor proteins, a complex family of plasma proteins made by three different polypeptides that are produced from four different genes. Salier, et al., The inter-a-inhibitor family: from structure to regulation. Biochem J, 1996. 351: p. 1-9.

In contrast to heterologous proteins produced by genetic recombination in mammalian cells, such as Chinese Hamster Ovary cells, TPPs derived from the cell lines of the present invention behave more normally since the secondary post-translational modifications required for complete function was preformed by the native hepatocyte manufacturing process. A significant advantage of 0 using the cells of the present invention to produce TPPs is that the producer cell line is of human 0 Sorigin and therefore leads to a more natural protein. Therefore, since a number of TPPs are synthesized by human hepatocytes, human hepatocyte-based expression systems of the cell lines of

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the present invention are used to produce TPPs in their "native" form.

Post-translational modifications of TPPs may affect bioactivity, clearance rate in vivo, immunogenicity and/or stability. The immortalized hepatocyte cell lines of the present invention 00 Snaturally perform the protein modifications, such as glycosylation, that are critical in the production of functional TPPs. The cell lines simultaneously produce multiple TPPs in culture, thus a sequential 00 0protein purification scheme will generate multiple products similar to plasma-derived proteins without the reoccurring risk of viral contamination.

TPPs secreted by our hepatocyte-based expression systems of the present invention behave more naturally than recombinant counterparts. For example, the inventors demonstrated that their immortalized human hepatocyte cell lines produce biologically active IaIp and are therefore a strong commercial source for this protein that cannot presently be produced by recombinant technology.

Thus, the inventors' production of Icap in its "native" form leads to a more effective, safe, and cost effective solution to treating life threatening diseases such as sepsis.

The hepatocyte-derived TPPs of the present invention provide a safe, effective, and cost efficient strategy to commercially produce native TPPs, which overcomes the shortcomings of the prior art.

Examples of uses for the cell lines of the present invention as production platforms, include, but are not limited to, the following: Production of hepatocyte-derived proteins. Cells maintained in suitable medium will naturally express proteins such as blood clotting factors factor VIII and Factor IX), albumin, a-1-antitrypsin, transferrin, inter-a-inhibitor proteins, growth factors, etc. that may be purified and used.

Use of recombinant DNA expression vectors to produce proteins of interest. For

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0example, the gene encoding a protein of therapeutic value may be recombined with controlling DNA segments containing a promoter with or without an enhancer

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sequence), transferred into the cell and then the protein produced may be harvested from the culture supernatant or a cellular extract by routine procedures well known in the art.

This may be accomplished by using one or more recombinant vectors that include: (1) 00 the gene encoding the protein to be expressed, a subunit of the protein to be expressed, or a 1 precursor of the protein to be expressed; and at least one control element affecting the 00 Stranscription of the gene, the control element being operably linked to the gene. The control element is typically a promoter or a promoter-enhancer combination. The characteristics of a suitable vector also include: an origin of replication; restriction endonuclease cleavage sites allowing the insertion of DNA encoding the desired genes; and a selection marker, typically one that confers antibiotic resistance. In one particularly preferred embodiment, the control elements comprise at least one promoter and at least one enhancer.

Suitable recombinant vectors include, but are not limited to, SV40-derived vectors, murine polyoma-derived vectors, BK virus-derived vectors, Epstein-Barr virus-derived vectors, adenovirus-derived vectors, adeno-associated virus-derived vectors, baculovirusderived vectors, herpesvirus-derived vectors, lentiviral-derived vectors, retrovirus-derived vectors, alphavirus-derived vectors, vaccinia virus-derived vectors, and others. Such vectors typically include a strong and constitutive promoter, at least one intron in the DNA to be expressed, and a polyadenylation signal at the 3'-terminus of the sequence to be transcribed.

The addition of a signal peptide to ensure appropriate post-translational modification, such as glycosylation, can be desirable. These vectors and characteristics of vectors are described in S.B. Primrose et al., "Principles of Gene Manipulation" 6 th ed., 2001, Blackwell, Oxford, England), pp. 174-201, G.L. Buchschacher, "Lentiviral Vectors" (1 s ed, 2003, Landes Bioscience, Georgetown, TX) and in T.A. Brown, "Gene Cloning and DNA Analysis: An 00 SIntroduction" (4 h ed., 2001, Blackwell, Oxford, England), all of which are incorporated Sherein by this reference.

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Methods for isolating DNA encoding plasma proteins to be expressed and for inserting such DNA into these vectors are also well known in the art. These methods are described, for example, in S.B. Primrose, "Principles of Gene Manipulation" 6 th ed., 00 Blackwell, Oxford, 2001), incorporated herein by this reference. In general, suitable DNA C1 for cloning can be obtained from reverse transcription of specific mRNAs, which can be 00 followed by application of the polymerase chain reaction (PCR) to amplify the DNA; such DNAs are generally known as cDNA. DNA can be inserted into the vectors by techniques that generally involve cleavage of the vectors with specific restriction endonucleases and insertion of the DNA at the cleavage sites.

Methods for transforming or transfecting the virally-immortalized human hepatocytes are well-known in the art and need not be described further in detail here. In general, such methods include, but are not limited to, lipofection, calcium-phosphate-mediated transfection, transfection mediated by DEAE-dextran, transfection by electroporation, transfection by biolistics, and transfection using polybrene. These transfection methods are described in J.

Sambrook D.W. Russell, "Molecular Cloning: A Laboratory Manual (3d ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 2001), vol. 3, ch. 16, incorporated herein by this reference.

In many cases, it is desirable to incorporate one or more reporter genes into the vector to assess the efficiency of transfection. The gene of choice is under the control of strong ubiquitous promoter-enhancer combinations. These include those from the immediate early genes of human cytomegalovirus, the Rous sarcoma virus long terminal repeat, or the human p-actin gene. An example of a suitable reporter gene is the chloramphenicol acetyltransferase (CAT) gene found in the Escherichia coli transposon. Detection of expression of the reporter gene can be done by a variety of techniques, such as detection of fluorescence or detection of radioactive products. Reporter genes and their assay are further described in M.A. Aitken et C al., "Gene Transfer and Expression in Tissue Culture Cells of Higher Eukaryotes," in Molecular Biomethods Handbook Rapley J.M. Walker, ed., Humana Press, Totowa, New Jersey, 1998), pp. 235-250, incorporated herein by this reference.

00 Once the protein has been expressed, it is then necessary to isolate the expressed protein. This is typically performed by standard methods for protein purification. These 00 methods include, but are not limited to, precipitation with salts such as ammonium sulfate, ion-exchange chromatography, gel filtration chromatography, reverse phase high pressure liquid chromatography, electrofocusing, chromatofocusing, and/or immunoaffinity chromatography, using any readily ascertainable property, such as protease activity, to detect the protein. Other purification methods are also known in the art. Protein purification methods are described, for example, in R.K. Scopes, "Protein Purification: Principles and Practice" (3d ed., Springer-Verlag, New York, 1994), incorporated herein by this reference.

In some cases, the expressed protein can be secreted from the cell into the surrounding culture medium. The efficiency of this process depends on the pattern of posttranscriptional modification, such as glycosylation, that the protein undergoes. This pattern affects the processing of the protein within the rough endoplasmic reticulum and the Golgi apparatus and its subsequent secretion. This is described in A.J. Dorer R.J. Kaufman, "Analysis of Synthesis, Processing, and Secretion of Proteins Expressed in Mammalian Cells" in Gene Expression Technology Goeddel, ed., Academic Press, San Diego, 1991), pp. 577-598, incorporated herein by this reference. The cloning vector can also be chosen so that the protein being expressed is fused to another protein, called a tag, which can be used to facilitate protein purification. Examples of tags include glutathione S-transferase, the MalE maltose-binding protein, and a polyhistidine sequence. The resulting fusion protein O0 can then be cleaved with specific proteolysis to remove the tag and result in purified protein.

Other Uses of the Nontumorigenic Virally-Immortalized Hepatocvte Cell Lines Other examples of uses for the cell lines of the present invention include, but are not limited to, the following: Studies of malignant transformation by chemical, physical and viral agents, and 00 Stransferred genes including oncogenes and high molecular weight genomic DNA from N tumors, using standard assays such as anchorage independent growth or tumor formation in 00 Sathymic nude mice. For example, a cloned viral oncogene k-ras (an oncogene present in many liver cell cancers) can be introduced into the hepatocyte cells using strontium phosphate transfection. The subsequent ability of the newly transfected cells to form tumors in mice as well as grow in an anchorage-independent fashion can be assessed.

Use of cells altered by transfer of oncogenes as in paragraph of this section above to screen for potential chemotherapeutic agents (by the techniques described in paragraph (1) of the "Toxicity and Metabolism Testing of Potential Therapeutic Drugs and Chemical Entities" section above) especially those which may be specific for cells transformed by the activation of particular oncogenes or combination of oncogenes.

Studies of cellular biochemistry, including changes in intracellular pH and calcium levels, as correlated with cell growth and action of exogenous agents including but not limited to those described in paragraphs and of this section above and paragraphs (1) through of the "Toxicity and Metabolism Testing of Potential Therapeutic Drugs and Chemical Entities" section above. To study intracellular pH and calcium levels, cells in suitable culture vessels are exposed to fluorescent indicator dyes and then fluorescence emissions are detected with a fluorescence spectrophotometer (Grynkiewicz et al, J. Biol.

Chem., 260:3440-3450 (1985)).

Studies of cellular responses to growth factors and production of growth factors: 00 Identification and purification of growth factors important for growth and differentiation of human liver hepatocyte cells. These cells are particularly useful for such an application since they grow in serum-free media. Therefore, responses to growth factors can be studied in precisely defined growth medium and any factors produced by the cells may be identified and purified without the complication of the presence of serum.

00 Studies ofintracellular communication by dye scrape loading assays, to rdetermine whether the cells growing in vitro have the ability to communicate via gap 00 junctions. The cultures may be scraped, with a scalpel, in the presence of a fluorescent dye in the growth medium. Cells at the edge of the wound are mechanically disrupted and therefore take up dye; whether intercellular communication has occurred may be ascertained by determining whether cells distant from the wound also contain dye.

Characterization of cell surface antigens: The cells are incubated with an antibody against the cell surface antigen of interest, and then reacted with a second antibody, which is conjugated to a fluorescent dye. The cells are then evaluated using a fluorescence activated cell sorter to determine whether they are fluorescent and therefore posses the cell surface antigen.

Cell-cell hybrid studies for identification of tumor suppressor activity (Stranbridge et al, Science, 215:252-259 (1982)). To determine whether these cell lines contain tumor suppressor genes, they are fused to malignant tumor cells. The presence of tumor suppressor genes is indicated by loss of malignancy as detected by loss of ability to form tumors in athymic nude mice, in the hybrid cells.

Identification of novel genes, including transforming genes in the naturally occurring cancer described in paragraph of this section above, growth factor genes as described in paragraph of this section above, tumor suppressor genes as described in paragraph of 00 this section above, using standard molecular biological techniques (Davis et al, Methods in SMolecular Biology, New York: Elsevier (1986)) and techniques such as cDNA subtraction cloning and similar processes.

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Growth of replicating hepatitis virus (as HBV, HCV, non-A non-B, HAV and other livertropic virus, CMV). Establishment of a clonal cell line of human liver hepatocyte cells containing replicating Hepatitis virus using methods oftransfection 00 o established for human liver cancer cells lines (Sells, M. A. et al, Proc. Natl. Acad. Sci., 'N 84:444-448). Using human liver hepatocyte lines, which contain HBV, the ability of HBV 00 Salone as well as in conjunction with chemical liver carcinogens such as aflatoxin B, can be evaluated for malignant transformation using anchorage independent growth assays as well as growth in athymic nude mice. Cell-cell hybrid techniques similar to those in paragraph of this section above can be used to evaluate possible inactivation of tumor suppressor genes by fusion with malignant cells before and after HBV transfection. The screening kits are easily assembled as other screening kits containing cell lines with other conventional components and labeling instructions for performing the test.

(11) The immortalized cells may be used as a way of expanding cells for liver transplant and liver function assist devices, both implanted and extracorporeal. Also, these cells can have additional genes transfected/infected into them for organ transplant for therapy of inherited metabolic disorders, especially those diseases associated with hepatic degradation -1 certain diseases are due to a deletion or abnormality of a particular gene). This gene 0 could then be transfected into our cells, and the cells then expanded for organ transplant.

(12) Studies of liver parasites: The immortalized hepatic cell lines could prove efficacious O for studying the life cycle of parasites that invade hepatocytes, including, but not limited to, amebiasis, malaria, nematodes, and roundworms.

(13) Studies of liver diseases: The immortalized hepatic cell lines could be used to study 00 Sdiseases of the liver, including, but not limited to, infectious liver diseases (such as C schistosomiasis, yellow fever, echinococcal cysts, amebiasis, and viral hepatitis); drug 00 induced hepatic disease (such as that from tranquilizers (phenothiazines), antibiotics (isoniazid), and anesthetics (halothane)); fatty liver (such as that from excessive caloric intake usually in the form of ethanol, hepatotoxins (CC14 and P0 4 and systemic metabolic disorders such as uncontrolled diabetes mellitus and toxemia of pregnancy); cirrhosis (such as that from dietary factors (usually alcohol), following massive necrosis from viral hepatitis, associated with pigment deposition, associated with disease of the bile ducts, and other miscellaneous cirrhoses); tumors; and hemochromatosis (a rare disorder of iron metabolism).

EXAMPLES

0 O The following examples are provided by way of describing specific embodiments of the present invention without intending to limit the scope of the invention in any way.

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Example 1 Characterization of Immortalized Human Hepatocytes Over 100 human hepatocyte clonal cell lines were established by transfecting human 00 hepatocytes with the SV40 large T and small t antigen genes under control of the SV40 early 1 promoter. Two cell lines designated EalC-35 and Fa2N-4 are described.

00 Both cell lines were created by lipofection-mediated transfection of primary cryopreserved human hepatocytes with vectors containing the SV40 largeT and small t antigens. The EalC-35 cell line was derived from transfection of cryopreserved human hepatocytes with an immortalization vector containing Blue Tag, a recombinant plasmid containing the early region of wild-type The Blue Tag vector was constructed as follows: PBR/SV (ATCC) was digested with restriction enzymes KpnI and BamHI to release a 2338 bp fragment (the 239-2468 bp fragment was discarded, with the remainder retained; numbering according to Fiers, W et al Science, 273:113-120) containing the SV40 early promoter and the coding regions from small t and large T antigens. This KpnI/BamHI fragment was inserted into the Bluescript SK vector (Stratagene) to produce Blue Tag; a Bluescript based vector that uses the SV40 promoter to drive T antigen expression. This early region was inserted into the Stratagene pBluescript SK vector backbone and was named pBlueTag.

Neomycin resistance was conferred on the transfected cells as a selectable marker by co-transfection of a neo plasmid. Clones were initially selected based on their ability to grow in G418 containing media. The EalC-35 cell line was established in MCT's proprietary serum containing media, CSM.

The EalC-35 cell line can be maintained in either CSM or MFE.

The Fa2N-4 cell line was immortalized via lipofection-mediated transfection with a single immortalization vector. The early region of the SV40 genome, contained in the 0 pBlueTag vector, was inserted into a backbone based upon the InvivoGen

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Splasmid and was named pTag-1. The T-antigen coding region is under the influence of a S hybrid hEF1-HTLV promoter. The vector also encodes a hygromycin resistance gene as a

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drug selectable marker. Clones were selected based on their ability to grow in hygro containing media. The Fa2N-4 cell line was established and maintained in MFE.

Example 2 00 Expression of Liver Specific Transcription Factors N Since retention of liver specific transcription factors is a prerequisite for expression of 00 0hepatic functions, clonal cell lines were initially screened by RT-PCR using primers for human HNF1, HNF3, HNF4a, HNF4y and C/EBP and albumin. Briefly, total RNA was prepared from 106 cells of each clonal cell line using the micro-isolation method of Brenner et al. (Message amplification phenotyping (MAPPing): a technique to simultaneously measure multiple mRNAsfrom small numbers of cells, Biotechniques 7(10): 1096-1103, 1989). 50 Rg ofE. coli rRNA (Sigma) was used as a carrier to facilitate the isolation of RNA from a small number of cells. RT-PCR reactions were carried out using the Perkin Elmer Cetus, GeneAmp RNA PCR Kit. One tg of total RNA was reverse transcribed using random hexamers and M-MLV reverse transcriptase according to the supplier's instructions. The PCR reaction was carried out using oligonucleotide primers that defined nucleotide fragments unique for each transcription factor. The primers were commercially synthesized and purified by Cruachem (Fisher Scientific). The PCR reaction was carried out for 30 cycles using an annealing temperature of 58 0 C for 1 min. The PCR products were visualized in a 1% agarose gel after staining with ethidium bromide. Positive control samples included RT- PCR analysis of total RNA of freshly isolated human hepatocytes (not shown). Both cell lines expressed all five hepatocyte associated transcription factors, as shown below in Table 1. Albumin production was measured as an indicator ofhepatocyte specific gene expression.

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00,> 0 As shown below in Table 1, both cell lines secrete albumin into the serum free conditioned medium as detected by ELISA assay using an antibody that recognizes human albumin.

Table 1 Clones HNF 1 HNF HNF HNF hC/EBP Albumin 3a 4a 4y (ug/mg protein)' Fa2N-4 2.79 0.3 00

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0", Example 3 Reverse-Transcription Polymerase Chain Reaction Analysis for Expression ofmRNA Transcripts RT-PCR analysis was performed on two immortalized human hepatocyte cell lines designated EalC-35 and Fa2N-4. Cells were plated on type I collagen coated dishes and maintained in MFE medium. Cultured cells were treated with rifampin (10 J.M) for 3 days or an equal volume of DMSO (control).

The following primers were used for the RT-PCR analysis: Albumin, Asialoglycoprotein II receptor, HNF-la, HNF-3, HNF-4 a, HNF4y, c/EBP, UGT 1A1, UGT 2B4, SXR, RXR a, RXRP, CAR, CYP1A2, CYP2A6, CYP2C9, CYP3A4, CYP2D6, CYP2E1, Cytochrome c, and NADPH.

RT-PCR analysis was performed on two immortalized human hepatocyte cell lines, and Fa2N-4, to screen for expression of hepatocyte specific transcription factors HNF-la, HNF-3, HNF-4 a, HNF4y, C/EBP), liver specific genes albumin and asialoglycoprotein receptor), transcription factors controlling drug metabolizing genes (e.g.

SXR, RXR a, RXRp, CAR) and phase I and phase II DMEs CYP1A2, CYP2A6, CYP2C9, CYP3A4, CYP2D6, CYP2E1, and UGT 1A1, UGT 2B4, respectively).

Analysis was performed with and without exposure to rifampin, a known 0 pharmacological inducer of CYP3A4 expression.

SRT-PCR analysis revealed that all transcripts examined were expressed by both cell

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lines but to various levels, as seen in Figures 1 through 8. Rifampin induction increased the expression of CYP3A4 transcripts. The legend for the gel loading order for Figures 1 through 8 is outlined in Tables 2 and 3 below.

00 Table 2 Legend for gel loading order for Figures 1 through 4 C" PCR Product Gel #1 Gel #2 Gel #3 Gel #4

C

#1 100bp marker 5 pl. 5 l 5 gl 5 l #2 EalC-35 p17, DMSO Ctrl UGT 1A1 SXR HNF-la Albumin #3 EalC-35 p17, Rifampin UGT 1A1 SXR HNF-la Albumin C #4 Fa2N-4 p34, DMSO Ctrl UGT 1A1 SXR HNF-la Albumin Fa2N-4 p34, Rifampin UGT 1A1 SXR HNF-la Albumin #6 Empty N/A N/A N/A N/A #7 EalC-35 p17, DMSO Ctrl UGT 2B4 RXRa HNF-3 ASGPR II #8 EalC-35 p17, Rifampin UGT 2B4 RXRa HNF-3 ASGPR II #9 Fa2N-4 p34, DMSO Ctrl UGT 2B4 RXRa HNF-3 ASGPR II Fa2N-4 p34, Rifampin UGT 2B4 RXRa HNF-3 ASGPR II #11 Empty N/A N/A N/A N/A #12 EalC-35 p17, DMSO Ctrl CAR RXR HNF-4a GAPDH #13 EalC-35 p17, Rifampin CAR RXRp HNF-4a GAPDH #14 Fa2N-4 p34, DMSO Ctrl CAR RXR3 HNF-4a GAPDH Fa2N-4 p34, Rifampin CAR RXRP HNF-4a GAPDH #16 Empty N/A N/A N/A N/A #17 EalC-35 p17, DMSO Ctrl c/EBP GAPDH HNF-4y N/A #18 EalC-35 p17, Rifampin c/EBP GAPDH HNF-4y N/A #19 Fa2N-4 p34, DMSO Ctrl c/EBP GAPDH HNF-4y N/A Fa2N-4 p34, Rifampin c/EBP GAPDH HNF-4y kit Ctrl Example 4 SV40 Mediated Proliferative Activity Primary human hepatocytes have limited proliferative activity when cultured. In order to overcome this characteristic, SV40 large T and small t antigens were introduced into the genome. The resulting clonal cell lines, Fa2N-4 and EalC-35 have subsequently been maintained in culture for up to 18 months. Both immortalized lines grow and function when maintained in MFE medium and can be cryopreserved and banked. Indirect immunofluorescent staining using polyvalent antibodies against large T antigen and albumin demonstrated that the cell lines continue to express the nuclear localized immortalizing gene (Figure 9a) as well as express a hepatocyte specific gene characteristic of differentiated function (Figure 9b). The morphology of the Ea IC-3 5 cell l ine is shown below (Figure 9c).

Table 3 Legend for gel loading order for Figures 5 through 8 I r PCR Product #1 11O0bp marker 5 P 5 iii 5 lil 5 j111 #2 JEaI C-35 p1 7, DM30 CtrI GYP 3A4 GYP 2D6 GAPDH,RT +),6000 Kit CtrI,61 0

GC

#3 JEa1C-35 p17, Rifampin GYP 3A4 GYP 2D6 GAPDH,RT(+),60 0 C Kit CtrI,60 0

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#4 IFa2N-4 p34, DM30 Ctrl GYP 3A4 GYP 2D6 GAPDH,RT(+),60 0 C Kit CtrI,59 0

C

IFa2N-4 p34, Rifampin GYP 3A4 GYP 206 GAPDH,RT(+),60 0 C Kit CtrI,60 0

G

#6 IEmpty N/A N/A IN/A N/A #7 EaIC-35 p17, DM30 Ctrl GYP-2G9 GYP 2E1 GAPDH,RT(+),6,oCN/A #8 Ea1C-35 p17, Rifampin GYP 2G9 GYP 2E1 GAPDH,RT(+),6,oC N/A #9 Fa2N-4 p34, DM30 Ctrl GYP 2G9 GYP 2E1 GAPDH,RT(+),6,oC N/A Fa2N-4 p34, Rifampin GYP 2G9 GYP 2E1 GAPDH,RT(+),6,oCN/A #11 Empty N/A N/A N/A N/A #12 EaIC-35 p17, DMS0 Ctrl GYP 1A2 cyt GAPDH,RT(+4),59oC N/A #13 Ea1C-35 p17, Rifampin GYP 1A2 Cyo GAPDH,RT(+)59oC N/A #14 Fa2N-4 p34, DM30 Ctrl GYP 1A2 Ct GAPDH,RT(+),59go N/A Fa2N-4 p34, Rifampin GYP 1A2 Cyo GAPDH,RT(+),59 0 C N/A #16 Empty N/A N/A N/A N/A #17 Ea1G-35 p17, DM30S Ctrl GYP 2A6 NADPH GAPDH,RT(-),60 0 G N/A #18 EaIC-35 p17, Rifampin GYP 2A6 NADPH GAPDH,RT(-),60 0 G N/A #1 a2N-4 p34, DM30 Ctrl GYP 2A6 INADPH GAPDH,RT-),60 0 G N/A Fa2N-4 p34, Rifampin GYP 2A6 INADPH GAPDH,RT(-),60 0 C N/A Immunostaining of Fa2N-4 cells for albumin expression was performed. Cells were plated on type I collagen and cultured in serum free medium for 72hr. Albumin was visualized by indirect immunofluorescence with a fluorescene conjugated secondary antibody. As shown in Figure 9b below virtually all of the cells express Albumin.

Example Druiz Metabolism Data Both cell lines continue to catalyze Phase I (GYP) and Phase HI conjugative reactions in monolayer cultures based on the metabolism of model substrates. One of the most important Phase I enzymes is CYP3A4, which is responsible for the metabolism of O0 0approximately 50% of all drugs. The expression of CYP3A4 can be modulated by many factors including multiple drug intakes that may induce or inhibit the overall expression of

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this CYP. Therefore the effective therapeutic dose of a drug is determined in part by CYP3A4 expression.

CYP3A4 modulators can be identified by monitoring the transcriptional 00 responsiveness of the gene and by measuring enzymatic activity towards model substrates C testosterone). For example, transcriptional responsiveness to prototypical 00 Spharmacological CYP3A4 inducers rifampin) can be assayed by the RT-PCR using specific primers to detect CYP3A4 cDNA. Rifampin-induced CYP3A4 enzymatic activity can also be measured by the production of the 6p-OH-testosterone metabolite when cells are incubated with testosterone. As shown below in Table 4, the Fa2N-4 cell line is more sensitive to CYP inducers than the EalC-35 cell line.

In order to demonstrate that the cell lines continue to express Phase II conjugating enzymes, cells were exposed to acetaminophen for 24 hours and conditioned culture medium was collected and analyzed for the production of acetaminophen glucuronide or acetaminophen sulfate conjugates. The production of the acetaminophen glucuronide and acetaminophen sulfate conjugates was measured by HPLC analysis. The results are shown in Table 4. To determine the effect of passage number, the production of acetaminophen glucuronide and acetaminophen sulfate was measured for Fa2N-4 cells after 11, 14, 27, 32, and 41 passages. For passage 41, ammonia clearance was also measured as an indicator of nitrogen metabolism. The results are shown in Table 5. These results indicate that both DME conjugative pathways are intact and that the Fa2N4 cells can remove ammonia.

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Table 4 Characteristics of the Fa2N-4 and Ea C-35 cell lines.

Cell line Rifampin Control Rifampin Acetaminophen Acetaminophen treated (ug 60-OH (ug 60-OH glucuronide sulfate CYP3A4 testosterone/mg testosterone/ (ug/mg protein) (mRNA fold protein)** mg protein) (ug/mg protein) induction)* Fa2N-4 15.4 5.44 15.28 20.9 16.1 (pl3) 2.2 4.53 9.25 15 21.5 (p29) Cells were exposed to vehicle or rifampin for 72 hours. Data is expressed relative to vehicle treated controls.

Cells were exposed to vehicle or rifampin for 72 hours and then incubated with testosterone for 24 hours. Production of the 6p-OH-testosterone metabolite was quantitated by HPLC analysis and data is expressed per mg total cell protein.

Table 5 Effect of Passage Number for Fa2N-4 Cells on Metabolism of Acetaminophen Cells Passage Acetaminophen Acetaminophen Ammonia Glucuronide Sulfate Clearance (ig/mg protein) (jg/mg protein) (mg NH 3 /mg protein/24hr) Fa2N-4 11 15.18 0.74 30.26 0.31 ND Fa2N-4 14 16.43 1.26 29.87 1.83 ND Fa2N-4 27 7.93 2.37 27.48 2.2 ND Fa2N-4 32 10.42 1.45 25.37 0.84 ND Fa2N-4 40 12.68 2.76 25.25 1.99 ND Fa2N-4 41 21.4 4.5 36.6 1.2 246 5.87 ND Not determined Example 6 Use of Immortalized Hepatocvtes to Identify and Rank CYP Inducers Two lines of evidence indicate that immortalized human hepatocytes can be employed to identify and rank CYP3A4 inducers based on 'induction potency".

First, exposing Fa2N-4 cells to rifampin (10 gM) results in a greater production of the 6-P testosterone metabolite than treating cells with weaker CYP3A4 inducers such as dexamethasone (50 tM) or phenobarbital (ImM), as shown below in Figure Secondly, immunoblot analysis demonstrated in Figure 11 that exposure of each of the cell lines to rifampin or phenobarbital for 48-72 hours increased expression of CYP3A4 0 protein in comparison to vehicle-treated controls; however, exposure to rifampin resulted in a 0 0 greater increase expression of CYP3A4 protein. The upper band in the immunoblot is nonspecific, and thus BNF, a CYP1A inducer, does not induce CYP3A4 protein expression.

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Taken together, these results clearly indicate that the immortalized human hepatocyte cell lines provide an invaluable model to detect constitutive and inducible CYP3A4 expression.

00 Example 7 C Morphological and Functional Similarity to Primary Cultures 00 0 Cultured Fa2N-4 cells are uniquely similar, both morphologically and functionally, to primary cultures of fresh human hepatocytes. Figure 12 shows this close morphological resemblance between human hepatocytes (upper panel) and Fa2N-4 cells (lower panel).

Numerous CYPs, including CYP1A2, CYP2B6, CYP2C9, and CYP3A4, are inducible in Fa2N-4 cells. The procedure for assessing enzyme induction in Fa2N-4 cells is remarkably similar to that for primary cultures of human hepatocytes.

The Fa2N-4 cells were propagated on a collagen substratum in MFE Support Medium. The cells were detached by trypsinization, isolated by centrifugation, and reattached to collagen in the desired format 12-, 24-, or 96-well plates). After a twoday adaptation period, the cells were treated once daily for three consecutive days with test article or the appropriate negative and positive controls. Enzyme induction was assessed 24 hours after the last treatment. CYP activity measured in microsomes prepared from the cultured hepatocytes (in vitro activity) was compared with that measured in microsomes prepared directly form human livers (ex vivo activity).

Enzyme induction was assessed in Fa2N-4 cells by incubating the cells with phenacetin (to measure CYP1A2), bupropion (to measure CYP2B6), diclofenac (to measure CYP2C9) or midazolam (to measure CYP3A4). In each case, the final concentration of substrate was 100 pM. Metabolite formation was determined by assaying aliquots of the cell O0 0 culture medium at various times (up to 8 hours) by LC/MS/MS. To facilitate a comparison of different CYP activities under a variety of conditions, the results were expressed relative to

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control activity determined at the 8-hour time point.

Fa2N-4 cells respond appropriately to enzyme inducers. As in the case of human hepatocytes, CYP1A2 is highly inducible by those agents that activate the Ah receptor, 00 whereas those agents that activate PXR and/or CAR cause induction of CYP3A4 and, to a "1 lesser extent, CYP2B6 and CYP2C9. As shown in Figure 13, treatment of Fa2N-4 cells 00 S(cultured in 6-well plates) with 100 jiM omeprazole caused marked induction of CYP1A2 activity, whereas treatment with 20 jiM rifampin induces CYP3A4 and, to a lesser extent, CYP2B6 and CYP2C9 activity.

Enzyme induction in Fa2N-4 cells is reproducible from one experiment to the next, and across different sized multi-well plates. Figure 14 depicts the results of a comparison of the reproducibility of induction of CYP2B6 (bupropion hydroxylase) activity by rifampin, across three different plate formats. Reproducibility of CYP1A2 and CYP3A4 induction across multiple cell passages was also assessed, and those results are shown in Figure The reproducibility in magnitude of induction across passages 32-47 is excellent for both CYP enzymes, and is superior to the reproducibility of induction typically seen with individual preparations of human hepatocytes. Induction of CYP2B6 in Fa2N-4 cells by rifampin is the same in 12-, and 24-well plates, as shown in Figure 16. Identical results were obtained for CYP2C9 (results not shown). These results indicate that differentiated properties of immortalized hepatocytes are highly stable. In terms of reproducibility, the immortalized hepatocyte cell lines of this present invention are superior to primary cultures of human hepatocytes, where the magnitude of CYP induction can vary substantially from one preparation to the next.

Enzyme induction in primary cultures of human hepatocytes is affected by the cell O0 Sculture format. Thus, as the well size decreases, there is a decline in the magnitude of enzyme induction in primary cultures of human hepatocytes.

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Figure 17 shows the effect of cell culture format on the induction of CYP 1 A2 by omeprazole and the induction of CYP3A4 by rifampin. Cell culture format appears to have a slight influence on CYP 1A2 induction in that the magnitude of induction was greater in a 6- 00 Swell than in a 12-, 24-, or 96-well format. However, in all cases, omeprazole induced N CYP1A2 activity by at least 9 fold over control. Figure 17 also shows, that in the case of 00 SCYP3A4, induction by rifampin is similar in the 12-, 24-, and 96-well format. Therefore, the cell lines of the present invention provide more reliable enzyme induction across many cell culture formats than do primary cultures of human hepatocytes.

The time course of CYP 1A2 and CYP3A4 induction in Fa2N-4 cells are similar to those observed in primary cultures of human hepatocytes. Figure 18 shows the time course of CYP1A2 and CYP3A4 induction in Fa2N-4 cells.

Enzyme induction in Fa2N-4 cells occurs over an appropriate range of inducer concentrations. The concentration-response curves for CYP1A2 induction by omeprazole and for CYP3A4 induction by rifampin in Fa2N-4 cells are shown in Figure 19. Similar results are observed in human hepatocytes.

Fa2N-4 cells respond appropriately to those compounds that do and do not induce CYP enzymes in human hepatocytes. For example, as in the case of human hepatocytes, compounds shown previously to activate PXR and induce CYP3A4 in human hepatocytes (Luo et al., CYP3A4 induction by drugs: Correlation between a pregnane X receptor reporter gene assay and CYP3A4 expression in human hepatocytes, Drug Metab. Dispos. 30: 795-804, 2002) induce CYP3A4 activity in Fa2N-4 cells, whereas Ah receptor agonists do not, as shown in Figure 20. Note that clotrimazole is both a CYP3A4 inducer and inhibitor, and thus 00

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0 CYP3A4 induction is masked by its inhibitory effect. Also, as in the case of human hepatocytes, CYP1A2 is highly inducible by those agents that activate the Ah receptor (as shown in Figure Table 6 summarizes the magnitude of induction of CYP1A2, CYP2B6, CYP2C9, and CYP3A4 in Fa2N-4 cells and primary cultures of human hepatocytes. In the case of CYP1A2, the magnitude of induction in Fa2N-4 cells was greater than the average fold induction in human hepatocytes. In the case of CYP2B6, CYP2C9 and CYP3A4, the magnitude of induction in Fa2N-4 cells was comparable to the median fold induction in human hepatocytes, but less than the average fold induction. Median induction differs considerably from mean induction in human hepatocytes because the latter is markedly affected by the occasional samples with extremely high values of fold induction. This is illustrated in Figure 21 for CYP3A4 induction, which ranges from zero (less than 1.5 fold) to 145 fold. Although the mean fold induction of CYP3A4 in human hepatocytes is 10 fold, the median induction, which is a more meaningful comparator, is about 4 fold.

Table 6 Comparison of CYP enzyme induction in Fa2N-4 cells and human hepatocytes r Enzyme Fa2N-4 Human hepatocytes Human hepatocytes (Inducer) Average induction Average induction Median induction (range) (range) CYP1A2 20 fold 13 fold 8.4 fold (Omeprazole (9.3 29) (2 56) or BNF) CYP2B6 2.5 fold 4.1 or 13 fold 2.9 or 8.5 fold (Rifampin) (2.0 3.9) (up to 14 or 71) CYP2C9 2.0 fold 3.5 fold 3.1 fold (Rifampin) (1.5 CYP3A4 5.1 fold 10 fold 3.8 fold (Rifampin) (4.0 6.9) (0 145) Data from Maden et al., Effects ofprototypical microsomal enzyme inducers on cytochrome P450 expression in cultured human hepatocytes, Drug Metab. Dispos. 31: 421- 431, 2003.

BNF (P-naphthoflavone) was the inducer for human hepatocytes, whereas omeprazole was the inducer for Fa2N-4 cells.

CYP2B6 activity based on 7-ethoxy-4-trifluoromethylcoumarin O-dealkylation (4 fold) or S-mephenytoin N-demethylation (13 fold).

0 Example 8

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0Use of the Immortalized Hepatocyte Cell Lines in Toxicity Studies Fa2N-4 and EalC-35 cells provide a human hepatocyte-derived system for

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conducting cell-based toxicity assays in vitro. Figure 22 illustrates the use of Fa2N-4 cells in

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toxicity testing.

Treatment of cells with toxic concentrations (up to 100 pM) of several agents (namely 00 3-methylcholanthrene, methotrexate, menadione, rotenone and troglitazone) caused a loss of 0, membrane integrity, resulting in the release into the medium of an intracellular enzyme, O0 0 namely alpha-glutathione S-transferase (a-GST), which was measured with Biotrin High Sensitivity Alpha GST EIA (Biotrin International, Dublin, Ireland). In contrast, little or no a-GST was released from Fa2N-4 cells treated with non-toxic concentrations of omeprazole, acetaminophen, probenecid, felbamate or rifampin.

It should be noted that some of these agents, such as acetaminophen and felbamate, cause clinically significant liver toxicity, but only at high doses (and hence at much higher concentrations than those used in the study depicted in Figure 22). For instance, acetaminophen toxicity is associated with doses exceeding 4 g/day as well as other concurrent environmental conditions. Exposure of the immortalized hepatocytes to the known toxicants 3-methylcholanthrene, methotrexate, menadione, rotenone, and troglitazone produced significantly greater release of a-GST from the cells.

Additional studies were conducted to compare the response of the Fa2N-4 cells with those of primary human hepatocytes, following treatment with 22 structurally diverse chemicals. Toxicity was assessed by measuring the release of lactate dehydrogenase (LDH) into the medium and a disruption of mitochondrial respiration (based on a decrease in resazurin reduction). The toxicity profiles of Fa2N-4 and primary hepatocytes were similar for most compounds, as summarized in Table 7 below. Some differences in the response of the two cell types were observed. The Fa2N-4 cells were more sensitive than primary hepatocytes to hepatotoxins such as troglitazone, hyperforin and benzo[a]pyrene, but were less sensitive to menadione.

Table 7 A comparison of the toxicity of 22 compounds in Fa2N-4 cells and primary human henatocvtes.

Cellular Response Non-toxic Compound Toxic Compound Same Rifampin 3-Methylcholanthrene Phenobarbital Methotrexate Phenytoin Rotenone Carbamazepine Efavirenz Troleandomycin Lansoprazole Omeprazole Probenicid Felbamate Acetaminophen Ciglitazone Sulfinpyrazone Simvastatin Fexofenadine Different Troglitazone Benzo[a]pyrene Hyperforin Menadione l A 11- FrazIN- cells more sensitive tman human hepatocytes Fa2N-4 cells less sensitive than human hepatocytes Thus, these immortalized hepatocytes will be suitable for specific in vitro toxicity screens. Furthermore, the immortalized hepatocytes offer the distinct advantages of reproducibility and access.

Example 9 Induction of Drug Metabolism Enzymes (DMEs) and Multidrup Resistan. 1 (M R 1' ui'cin the Fa2N-4 Cell Line Treatment of the Fa2N-4 cells with drug was initiated 48 hours after plating. For RNA quantification, cells were exposed to drug for 48 hours. Gene expression was monitored in Fa2N-4 cells by the Invader assay (Third Wave Technologies, Madison, WI), a robust, yet simple, high-throughput system for quantification ofmRNA transcripts.

CYP1A2, CYP3A4, CYP2C9, UGT1A, and MDR1 transcripts were quantified from total 0 RNA extracts from Fa2N-4 cells treated with a panel of known inducers and compared with Svehicle controls.

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Enzyme activity assays were also used to monitor the induction of CYP1A2, CYP2C9, and CYP3A4. For enzyme activity studies, cells were exposed to drug for 72 hours. CYP3A4 activity was determined by measuring the extent of 6-beta- 00 hydroxytestosterone formation from testosterone by mass spectrometry. CYP2C9 activity C1 was determined by measuring the extent of 4'-hydroxydiclofenac formation. CYP1A2 00 activity was determined by measuring the extent of O-dealkylation of 7-ethoxyresorufin.

Metabolites were quantified by comparing measurements to standard curves.

The Fa2N-4 cells responded in a similar manner as primary human hepatocytes.

Treatment with 10 gM rifampin resulted in increases in CYP3A4 mRNA (17-fold) and activity (6-beta-hydroxytestosterone formation, 9-fold); and in CYP2C9 mRNA (4-fold) and activity (4'-hydroxydiclofenac formation, 2-fold). Treatment with 50 jtM beta-napthoflavone resulted in increases in CYP1A2 mRNA (15-fold) and activity (7-ethoxyresorufin 0dealkylation, 27-fold). UGT1A mRNA was induced by beta-naphthoflavone (2-fold), and MDR1 (P-glycoprotein) mRNA was induced by rifampin (3-fold). Table 8 summarizes the induction data in Fa2N-4 cells for three CYPs expressed as fold-increase in mRNA compared to published data in primary hepatocytes.

Table 8 Summary of reported inductive response in Fa2N-4 cells as compared to response of primary human hepatocytes Parameter Inducer Fa2N-4 cells Primary cells Fold-increase Fold-increase CYP1A2 B-Naphthoflavone 1.5 13 CYP2C9 Rifampin 3.8 Phenobarbital 2.6 1.8 CYP3A4 Rifampin 17 Phenobarbital 9.3 3.3 0 In addition to examining the inductive effect of a single concentration of drug, the O0 SFa2N-4 cells can also be used to look at dose-response relationships. For example, values were calculated based on the response of Fa2N-4 cells dosed with multiple

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concentrations ofrifampin ranging from 100 nM to 50 tM. Figure 23 contains EC50 plots for Fa2N-4 cells using increased CYP3A4 transcript values (Figure 23A), as well as increased CYP3A4 enzyme activity (Figure 23B). The calculated EC50s were 0.43 pM 00 S(r =92) and 0.77 pM (r 2 for the transcript and enzyme activity, respectively. In addition, 00 the calculated maximum induction (Imax) values were 13-fold for the transcript endpoint and S9.7-fold for the enzyme activity endpoint.

Multiple passages of the Fa2N-4 cells have been tested for CYP3A4 induction.

Figure 24 shows response of multiple passages of Fa2N-4 cells to a CYP3A4 inducer with a weak response (50 piM dexamethasone striped bars) and a CYP3A4 inducer that exhibits a strong response (10 pM rifampin black bars). The open bars denote the values for cells treated with DMSO vehicle alone. Treatment with dexamethasone increased CYP3A4 transcripts, 1.6-fold and 1.5-fold at passages 21 and 36, respectively. Treatment with 10 pM rifampin increased CYP3A4 transcripts, 17-fold and 16-fold at passages 21 and 36, respectively (Figure 24A). CYP3A4 enzyme activity was increased 2.1-fold and 2.0-fold for dexamethasone and 8.9-fold and 4.9-fold for 10 pM rifampin at passages 28 and 36, respectively (Figure 24B).

Figure 25 compares various multiwell formats. Regardless of the plate format, Fa2N- 4 cells exhibit substantial CYP3A4 inductive response to rifampin. Fold changes in CYP3A4 transcript were 17.1-fold when using a 24-well plate, 6.6-fold when using a 48-well plate, and 5.7-fold when using a 96-well plate.

These results show that the immortalized hepatocyte cell lines of the present invention, specifically Fa2N-4 cells, can be a reliable surrogate for primary human hepatocytes, and can provide for a reliable assessment of induction of DMEs and 0 O transporters.

Example 0 Expression of Plasma Proteins By Fa2N-4 and EalC-35 Cell Lines

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The well-differentiated nature of these cell lines is further supported by their continued secretion of adult hepatocyte function specific plasma proteins (Figure 26). Culture 00 medium was harvested from Fa2N-4 and EalC-35 cells seeded into either 60 mm plates or N roller bottles and analyzed by Western blot analysis. Medium was concentrated 50X by 00 Sultrafiltration and 40 pg of total protein was loaded per lane except for albumin (10 pIg total protein/lane). Blots were incubated with either monoclonal or affinity purified polyclonal antibodies against albumin, a-l-antitrypsin, Factor VIII and Factor IX and visualized using secondary antibodies conjugated to horseradish peroxidase followed by incubation with DAB substrate. As shown below in Figure 26, both cell lines continue to express albumin, a-1antitrypsin, and Factor IX at similar levels per ml when maintained in roller bottles as cultures maintained in plates. The expression of Factor VIII was variable and highly dependent on cell line and culture conditions. There was heterogeneity in the processing of Factor IX, an observation also seen in the human plasma-derived protein.

Both AAT and IaIp are plasma proteins that inhibit the proteolytic activity of trypsin.

As shown in Figure 26 below, immunoblot analysis clearly demonstrated the presence of AAT in the conditioned medium from both cell lines.

Taken together, all the above examples strongly indicate that the immortalized human hepatocyte cell lines of the current invention, including but not limited to the Fa2N-4 and cell lines, maintain many functional attributes characteristic of hepatocytes in vivo and are an invaluable in vitro system to produce TPPs.

Example 11 00 Production of albumin.

SFa2N-4 cells were grown to confluence in T-150 flasks in serum free medium and 0 albumin production was measured by an ELISA assay. The results of this assay are found in Table 9 below. At passages 13 and 16, the Fa2N-4 cells produced approximately 3 pg/ml of albumin. At passage 33 the Fa2N-4 cells produced approximately 9 pg/ml of albumin and at 00 passage 41 the Fa2N-4 cells produced approximately 6 pg/ml albumin. Therefore, the 00 immortalized hepatocyte cell lines of the present invention, specifically Fa2N-4 cells, are a 0 O potential source for the production of the TPP albumin.

Table 9 Concentration of albumin in FA2N-4 cells measured by ELISA assay Cells Passage Albumin in Media (pg/ml) Fa2N-4 13 3.73 0.64 Fa2N 16 3.06 0.11 Fa2N 33 9.5 Fa2N 41 6.17 0.29 Example 12 Expression of inter-alpha-inhibitor proteins (Iclp).

Inter-a-inhibitor proteins (Ialp), natural serine protease inhibitors found in relatively high concentration in plasma have been shown to play roles in inflammation, wound healing and cancer metastasis. Ialp is a family of plasma proteins made and secreted by hepatocytes.

The major forms of Ialp are inter-a-inhibitor (lal, containing one light chain peptide called bikunin and two heavy chains) and pre-ac-inhibitor (Pal, containing one light and one heavy chain). Recently, a monoclonal antibody that recognizes the light chain of human IcIp (MAb 69.31) was developed by scientists at Prothera Biologics (Providence, Rhode Island).

Using MAb 69.31 in a competitive ELISA, these investigators demonstrated that plasma lalp levels were significantly decreased in severe septic patients compared to healthy controls oo (Lim YP, Bendelja K, Opal SM, Siryapom E, Hixson DC, Palardy JE. Correlation 0 0 Between Mortality and the Levels of nter-alpha Inhibitors in Plasma of Severely Septic O Patients. Journal of Infectious Disease, 188:919-926, 2003).

0 C Western blot analysis, using MAb 69.31 revealed that both the Fa2N-4 and cell lines continue to synthesize immunoreactive IaIp (data not shown). Subsequently, the Samount of Ialp secreted into the condition medium was quantitated using an ELISA assay 00 (see example 14 below). Thus, the Fa2N-4 and EalC-35 cells are a potential source for the 00 production of the TPP Ialp.

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SExample 13 Production of transferrin by immortalized human hepatocytes In order to determine if the EalC-35 and Fa2N-4 cells from various passages made and secreted transferrin, the cells were cultured in serum free medium without transferrin for 7 days. Conditioned culture medium was collected after 7 days and immunoblot analysis was performed using a commercially available antibody against transferrin. Human plasma was used as the positive control. Immunoblots using an antibody against transferrin revealed that the cells from all passages continue to express this plasma protein, as shown in Figure 27.

Lanes -2-5 show EalC-35 cells from different passages produce transferrin that is nearly identical to plasma-derived transferrin. Lanes 6-9 show Fa2N-4 cells from different passages produce transferrin that is nearly identical to plasma-derived transferrin Thus, the claimed immortalized hepatocytes, including but not limited to the Ea C-35 and Fa2N-4 cell lines, are a potential source for the production of transferrin.

Example 14 00 STrypsin Inhibition Assay and Ouantitation of inter-alpha inhibitor protein (Ialp) present in conditioned medium

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C, The total trypsin inhibitory activity of the conditioned media includes the activity from the major serine protease inhibitors, a-l-antitrypsin and Ialp. The amount of trypsin inhibition activity secreted into the condition medium by EalC-35 and Fa2N-4 cells was 00 Smeasured using the chromogenic trypsin substrate L-BAPA (N(alpha)-Benzoyl-L-arginine-4nitroanilide hydrochloride, Fluka Chemicals) (see Table 10). The assay is based on the 00 Sability of serine protease inhibitors to inhibit the hydrolysis of L-BAPA. Inhibition can be monitored by a decrease in the rate of delta absorbance/minute at 410 nm. The specific activity was calculated based on the biological activity per tg cellular protein. EalC-35 cells expressed 115 TIU/mg of protein and Fa2N-4 cells expressed 45 TIU/mg of protein.

Table 10 Trypsin inhibition activity and Ialp in EalC-35 and Fa2N-4 cells Cultured Protein Conc. after 50x Trypsin Inhibition IaIp conc.

media ultrafiltration (UF) [mg/mL] Activity after UF after UF [TIU/mg] Ig/mL] 4.50 115.0 20.08 Fa2N-4 9.02 45.10 4.03 The amount of IaIp in the media was measured by a competitive ELISA using MAb 69.31 a polyclonal antibody specific against human Ialp). The ELISA was performed as follows: 96 well Immunolon-4 plates (Dynex, USA) were coated with purified Ialp (300 ng) in 50 mM carbonate buffer pH 9.6 and incubated overnight at 4"C. A serial dilution of purified human plasma derived IaIp in PBS containing 1% rat serum was used to establish a standard curve. For the quantitative analysis of Ialp levels in culture media, 50 tL of media or serially diluted Icdp were added to individual wells of a 96 well plate. After the addition of 50 uL of MAb 69.31 to each well, plates were incubated for 1 hr at 37°C and subsequently washed using an automated plate washer (Labsystem). The bound MAb 69.31 was detected by adding HRP-conjugated goat anti-mouse IgG (human absorbed) (Biosource, Camarillo, 0 0CA, USA) for 1 hr at 37C. After washing, 100 UL 1-Step ABTS (Pierce, Rockford, IL, USA) was added to the wells and the absorbance at 405 nm was measured on ELISA plate

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reader (BioTek). Each sample was tested in triplicate. Unconditioned culture media was used as baseline control. The results are summarized in Table 10. EalC-35 cells expressed .tg/ml of IcIp and Fa2N-4 cells expressed 4 pg/ml of Iolp.

00 These results demonstrate that the immortalized hepatocytes of this invention are a 00 good potential source for the production of TPPs, such as AAT and Ialp.

SExample Two-Dimensional Gel Analysis 2-D gel electrophoretic analysis was used to separate the secreted proteins of the Fa2N4 and EalC35 cell lines. Using Invitrogen's ZOOM IPGRunner system, the first IEF separation of the proteins was carried out using fixed pH gradient strip (pH range of 3-10) followed by the second dimension separation using 4-12% Tris-Gycine SDS-PAGE. In both cell lines multiple spots of proteins could be identified as possible candidates for TPPs.

(Fig.28A. Fa2N4; 28B, EalC35). After the 2-dimensional gel separation the secreted proteins of the Ea C35 cell line were transferred onto nitrocellulose and Western blot analysis using anti-Factor IX antibody was performed. Reactive protein with MW of 70 KD and pi 6.5-7.0 was detected (Fig.28C). Thus, the claimed immortalized hepatocyte cell lines of the present invention are a potential source of TPPs, such as Factor IX.

Example 16 Cell Line Expansion and Quantitation of Plasma Protein Secretion The economical production of TPPs using cultured immortalized human hepatocytes as producer cells can only be accomplished if the cells continue to make and secrete these TPPs when expanded in mass culture. In order to initially evaluate this question, Fa2N-4 cells were grown to confluence in T25, T75 and T150 culture flasks and selected plasma 0 proteins were quantitated using ELISA assays in combination with capture antibodies that o recognized albumin, AAT or Iclp. An equivalent number of cells were initially plated per 0 C) square cm, 5, 15 and 30 million cells, respectively. Conditioned medium was collected for 3 days, pooled, concentrated 10 Ox by ultrafiltration and assayed. As shown in Figure 29 below, the total expression of each plasma protein was approximately proportional to cell number.

00 Values represent the mean SD for triplicate samples. Over the 3-day period cells cultured 0 in T150 flasks produced approximately 200 tg albumin, 500 ng Ioalp and 150 ng AAT. This 00 Sshows that the immortalized hepatocyte cell lines claimed in the present invention are a potential source for the production of TPPs.

Example 17 Effect of Culture Period on Albumin Secretion We plan to use immortalized human hepatocytes as biofactories for the commercial production of TPPs. Therefore, it is essential that TPP secretion must not be significantly decreased in long-term culture. We recently initiated a study in order to evaluate this question, Fa2N-4 cells were grown in T25, T75 and T150 culture flasks, as described above in the previous examples, and albumin production was measured as an indicator of overall protein secretion. Conditioned medium was collected on Day 3; cells were re-fed and resampled on Day 6. Albumin secretion was analyzed by an ELISA assay. The results indicate that albumin secretion continues to increase over the 6 day collection period irrespective of the plating format (see Figure 30). Of particular note, there is a dramatic increase in albumin when cells were cultured in the T75 and T150 flasks. Since total cellular protein does not significantly increase with time in culture (data not shown), it seems likely that these results are due to enhanced production as a result of adaptation to culture conditions and not the result of a dramatic increase in cell number per flask.

00 Example 18 O Effect of Tumor Necrosis Factor a (TNFa) on Plasma Protein Secretion o Production of some plasma proteins can be modulated by acute phase proteins, such

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IN as TNFa in vivo. The effect of treatment with TNFa on the secretion of AAT was studied.

Fa2N4 cells were maintained in serum free proprietary MFE medium containing TNFa 1, OO 5, or 10 ng/ml) for 3 days. As shown in Table 11 below, the secretion of ATT was most notably increased by the inclusion of 5 ng/ml TNFa in the serum free culture medium.

00 Values are the average of duplicate samples. Thus, it may be possible to increase ATT Sproduction using this cytokine. Therefore, treatment of the immortalized hepatocyte cell lines of the present invention with TNFa may be an effective way to increase the production of TPPs.

Table 11 Effect of TNFa on TPP expression Antitrypsin Concentration of Tumor (ng)/p g Antitrypsin Sample Necrosis Factor Alpha Protein well #1 TNF 0 ng/ml 0.21 14.00 #2 TNF 1 ng/ml 0.34 21.00 #3 TNF 5 ng/ml 0.43 44.73 #4 TNF 10 ng/ml 0.48 32.93 Example 19 Effect of dexamethasone on expression of plasma proteins by immortalized human hepatocytes Albumin expression is regulated in part by a dexamethasone inducible promoter (Nakmura, et al, J Biol Chem, 261:16883-16888, 1986). In order to examine the effects of dexamethasone on the production and secretion of albumin by immortalized human hepatocytes, Fa2N-4 cells (passage 32) were cultured on type I collagen dishes with or without dexamethasone in the culture medium for 48hrs and albumin expression was measured by an ELISA assay. Values represent the average of duplicate samples. As summarized in Table 12 below the secretion of albumin was significantly decreased in the absence of dexamethasone.

Therefore, treatment with dexamethasone may be an effective way to increase the production of TPPs in the claimed immortalized hepatocyte cell lines of this present invention.

Table 12 Effect of dexamethasone on TPP expression Concentration of Dexamethasone Albumin (pg/ml) 0 40.0 tM 100.0 Example Ability to Produce and Express Therapeutic Plasma Proteins (TPPs) The ability of our Fa2N-4 cell line to correctly produce an immunologically reactive TPP was illustrated with the production of immuno-reactive human growth hormone (hGH).

On the day prior to transient transfection, Fa2N-4 cells were plated at a density of0.5-0.8x10 6 cells per well in six-well Nunc plates using 10% NBCS-MFE medium. On the day of transfection the cells were washed one time to remove serum and a CMV-based plasmid, containing the complete cDNA for hGH, was transiently transfected into the Fa2N-4 cells using either an Invitrogen Lipofectamine Plus or a Qiagen Effectene transfection reagent kit.

The transfections were performed as per the manufacturers' protocols.

Conditioned media was withdrawn from each well after 24 and/or 48 hours and was subsequently used for an ELISA-based immunodetection assay. The ELISA assay is a colorimetric enzyme immunoassay for the quantitative determination of secreted hGH utilizing the sandwich ELISA principle. Microtiter plate pre-bound antibodies to hGH bind to secreted hGH contained in the conditioned media. Subsequently, a digoxigenin labeled hGH antibody binds to a second epitope of the hGH peptide contained in the conditioned media and retained on the microtiter plate. An antibody to digoxigenin, which is conjugated 0C) to peroxidase, is then added and followed by the peroxidase substrate ABTS. The peroxidase- C) catalyzed cleavage of the substrate yields a colored reaction product that can be easily detected using a microtiter plate reader.

C) Our results confirm that using either transfection kit and harvesting the conditioned media at either 24 or 48 hours post-transfection, the Fa2N-4 cells produce extraordinarily large quantities of double immunodetected liGH while transfection with LacZ or no plasmid 00 negative controls produced no detectable levels of hGH. A photograph of the ELISA plates 1 and 2 are shown in Figure 31 and Figure 32, respectively. The key for Figures 31 and 32 is 00 C) shown below in Table 13.

Table 18 Legend for ELISA plates shown in Figures 31 and 32 Plata I 1 2 3 4 5 6 7 a 9 10 11 12 A Blank Std 0 Std 80 lOLacZ 2 10(1:10)3 10(1:30)1 IlNog2' 10(1:10)3' 10(1:30)1' 2OLacZ 2 20(1:10)3 20(1:30)1 B Blank Sid 0 Sid 80 lQLacZ 2 10(1:10)3 10(1:30)1 INeg2' 10(1:10)3* 10(1:30)1* 20LacZ 2 20(1:10)3 20(1:30)1 c Blank Std 10 Sid 160 lOLacZ 3 10(1:20)1 10(1:30)2 lNeg3' 10(1:20)1' 10(1:30)2' 2OLacZ 3 20(120)1 20(1:30)2 D Blank Sid 1 0 S d 160 lOLacZ 3 10(1:20)1 10(1:30)2 1lNeg3' 10(1:20)1' 10(1:30)2' 2OLacZ 3 20(1:20)1 20(1:30)2 E Blank Sid 20 Sid 320 10(1:10)1 10(1:20)2 10(1:30)3 10(1:10)1' 10(1:20)2' 10(1:30)3' 20(1:10)1 20(1:20)2 20(1:30(3 F Blank Std 20 Sid 320 10(1:10)1 10(1:20)2 10(1:30)3 1Q(1:10)1' 10(1:20)2Z 10Q(1:30)3* 2Q(1:10)1 20(1:20)2 20(1:30)3 G Blank Std 40 lOLacZ 1 10(1:10)2 10(1:20)3 1INegi' 10(1:10)2' 10(1:20)3' 2OLacZ 1 20(1:10)2 2Q(1:20)3 Maegi' H Blank Std 40 IOLacZ 1 10(1:10)2 10(1:20)3 1INegi' 10(1:10)7 10Q(1:20)3' 2OLacZ 1 20(1:10)2 20(1:20)3 2Negil Plate 2 1 2 3 4 5 6 7 8 9 10 1l 12 A Blank 2Nog3' 20(1:20)1' 20(1:30)2' (LacZ 3 1(1.0)1 1(2.0)2 Blank' B Blank 2Neg3Y 20(1:20)1* 20(1:30)2' ILac:Z 3 1(1.0)i1 (2.0)2 Blank' c Blank 2Q(1:10)1' 20(1:20)Z' 20(1:30)3*1(0.5)1 1(1.0)2 1(2.0)3 Blank' D Blank 20(1:10)1' 20(1:20)7' 20(1:30)3 1(0.5)1 1(1.0)2 1(2.0)3 Blank E Blank 20(1:10)Z 20(1:20)3' (LacZ 1 1(0.5)2 1(1.0)3 Blank' F Blank 20(1:10)2' 20(1:20)3' (LacZ 1 1(0.5)2 Blank' G Blank 2Neg2' 2Q(1:10)3' 20(1:30)1' U~cZ 2 1(2.0)1 Blank' H Blank 2Neg2' 2Q(1:10)3' 20(1:30)1' tLacZ 2 1(0.5)3 1(2.0)1 Blank! Key- Blank=Substrate Sid X=Slandard of X ngfm( hGH XOLacZ Y--Sample Y obtained X days after transfectlon of a LecZ control plaamld Into 0.5x10(6) cella using the Oilgen kdt XO(1:Y)Z=Sample Z obtained X days after transfection of a 1:Y ratio of DNA:Effectene reagent Into 0.6x1O(6) cans using the Olagen kit XNegY'Sample Y obtaiaed X days after transfeetion of no DNA into 0.8x10(6) cells using the Olagen kit X0(1 -Y)Z'=Sanp~e Z obtained Xdays after iransfecion of a 1:Y ratio of DNA:Effectene reagent Into 0.8x10(B) cella using (lhe Olagen kit (LacZ X=Sarmpta X obtained one day after transfection of a LacZ control plasmid Into 0.7x1O(6) cells using the Invitrogen kit l(X)Y=Sample Y obtained one day after transfection of Xug DNA Into 0.7x10(6) cells using the (nvitrogen kit Blank'=Buffer Example 21 Immunophehenotpic characterization of the EA 1C-3 5 and Fa2N-4 cell lines Both the EalC-35 (passage 26) and Fa2N-4 (passage 30) cell lines were phenotyped by indirect immunofluorescence analysis using a panel of antibodies against different 00

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t(N 00q hepatocyte or bile duct markers as well as against the SV40 immortalizing gene. The results from this analysis are summarized in the Table 14 below: Table 14 Expression of various hepatocyte and bile duct markers and the SV40 immortalizing gene in EalC-35 and Fa2N-4 cells Marker EalC-35 Fa2N-4 positive Cells) positive Cells) Albumin 90 100 Alpha Fetoprotein 0 0 Connexin 32 50 CD 81 100 100 CD49f (integrin 0 0 alpha 6 chain) T-antigen 100 100 0 The expression ofconnexin 32 was density dependent. When cells grew to confluent monolayers, a subpopulation of EalC-35 and Fa2N-4 cells express this gap junctional protein that is only expressed by hepatocytes in adult liver tissue.

All cells expressed SV40 T-antigen, the immortalizing gene. Expression of immunodetectable SV40 T-antigen was localized specifically to the nucleus. The welldifferentiated nature of the immortalized liver cells is indicated by the strong expression of the adult hepatocyte specific lineage markers, albumin and connexin 32 and the lack of the fetal hepatocyte marker, alpha fetoprotein. The cells do not express CD49f, a bile duct marker. The cells express CD81, the putative receptor for hepatitis C virus glycoproteinmediated viral infection. A photomicrograph of Fa2N-4 cells immunostained for CD81 is shown in Figure 33. Note that expression of CD81 is localized to the plasma membrane.

OTHER EMBODIMENTS All references discussed above are herein incorporated by reference in their entirety for all purposes. While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention as defined by the appended claims.

SThe entire disclosure in the complete specification of our Australian Patent Application 0 SNo. 2004322811 is by this cross-reference incorporated into the present specification.

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00 00 0-,

Claims

1. A virally-immortalized hepatocyte, said hepatocyte being derived from a normal liver cell; O is nontumorigenic; and -IN naturally produces endogenous therapeutic plasma proteins (TPPs).

2. The hepatocyte according to claim 1, wherein said hepatocyte is derived from 00 a human liver cell. S3. The hepatocyte according to claim 1, wherein said hepatocyte is derived from 00 primary cryopreserved human hepatocytes.

4. The hepatocyte according to claim 1, wherein said hepatocyte comprises substantially pure simian virus 40 (SV40) DNA. The hepatocyte according to claim 4, wherein said DNA encodes wild type large T and small t antigens (TAg).

6. The hepatocyte according to claim 5, wherein said SV40 TAg interacts with a tumor suppressor.

7. The hepatocyte according to claim 6, wherein said tumor suppressor comprises human Rb.

8. The hepatocyte according to claim 6, wherein said tumor suppressor comprises human p53.

9. The hepatocyte according to claim 1, wherein said hepatocyte has the ability to be maintained in serum free media. The hepatocyte according to claim 9, wherein said serum free media is MCT's proprietary serum free media.

11. The hepatocyte according to claim 10, wherein said MCT's proprietary serum free media is Multi-Functional Enhancing media (MFE).

12. The hepatocyte according to claim 1, wherein said hepatocyte retains hepatic 0 Sfunction.

13. The hepatocyte according to claim 12, wherein said hepatic function is the O ability to continue to express hepatic enzymatic activity.

14. The hepatocyte according to claim 13, wherein said hepatic enzymatic activity is cytochrome P450 (CYP) enzymatic activity. 00 The hepatocyte according to claim 13, wherein said hepatic enzyme activity of ,1 said hepatocyte can be used to assess the effect of chemical entities on the liver. 00

16. The hepatocyte according to claim 13, wherein said hepatic enzyme activity of said hepatocyte can be used to assess the effects of drug candidates on the liver.

17. The hepatocyte according to claim 13, wherein said hepatic enzyme activity of said hepatocyte can be used to assess enzyme induction.

18. The hepatocyte according to claim 13, wherein said hepatic enzyme activity of said hepatocyte can be used to assess cellular toxicity.

19. The hepatocyte according to claim 13, wherein said hepatic enzyme activity of said hepatocyte can be used to assess the effect of the liver on chemical entities. The hepatocyte according to claim 19, wherein said hepatocyte can be used to assess drug metabolism.

21. The hepatocyte according to claim 19, wherein said hepatocyte can be used to assess species comparisons.

22. The hepatocyte according to claim 12, wherein said hepatic function is the ability to form an acetaminophen conjugate.

23. The hepatocyte of claim 1, wherein said TPPs are selected from the group consisting of albumin, a-1 antitrypsin, blood clotting factors, transferrin and inter-a inhibitor proteins (Icap).

24. The hepatocyte according to claim 23, wherein said TPPs consist of at least a 00 O significant amount of albumin. The hepatocyte according to claim 23, wherein said TPPs consist of at least a 0 significant amount of a-1 antitrypsin. \0

26. The hepatocyte according to claim 23, wherein said TPPs consist of at least a significant amount of a blood-clotting factor. 00 N

27. The hepatocyte according to claim 26, wherein said blood clotting factor is cN factor VIII or factor IX. 00

28. The hepatocyte according to claim 23, wherein said TPPs consist of a significant amount oftransferrin.

29. The hepatocyte according to claim 23, wherein said TPPs consist of at least a significant amount ofinter-a-inhibitor proteins (lalp). The hepatocyte according to claim 1, wherein said hepatocyte can be used to perform a procedure selected from the group consisting of: studies of malignant transformation by chemical, physical and viral agents, and transferred genes including oncogenes and high molecular weight genomic DNA from tumors, using standard assays such as anchorage independent growth or tumor formation in athymic nude mice; use of cells altered by transfer of oncogenes to screen for potential chemotherapeutic agents; studies of cellular biochemistry, including changes in intracellular pH and calcium levels, as correlated with cell growth and action of exogenous agents; 00 studies of cellular responses to growth factors and production of O Sgrowth factors; 0 studies of intracellular communication; O O characterization of cell surface antigens; cell-cell hybrid studies for identification of tumor suppressor activity; 0 identification of novel genes; growth of replicating hepatitis virus (as HBV, HCV, non-A non- O B, HAV and other livertropic virus, CMV); 0 identification of new drugs to treat hepatitis C virus (HCV) infection; (11) expanding of cells for liver transplant and liver function assist devices, both implanted and extracorporeal; (12) studies of liver parasites; (13) studies of liver diseases; (14) identification of potential therapeutic drugs; (15) identification of new drug targets; (16) identification of chemical and biological agents that induce terminal differentiation; (17) studies of the metabolism of carcinogens and other xenobiotics; (18) studies of DNA mutagenesis; (19) studies of chromosome damaging agents; studies of cytotoxicity of drugs, chemical entities, carcinogens, and xenobiotics; (21) production of hepatocyte-derived proteins; and (22) use of recombinant DNA expression vectors to produce proteins of interest. 00

31. The hepatocyte according to claim 1, wherein said hepatocyte is Fa2N-4 O S(ATCC PTA-5566).

32. The hepatocyte according to claim 1, wherein said hepatocyte is O S(ATCC PTA-5565).

33. A virally-immortalized human primary hepatocyte cell line Fa2N-4 (ATCC PTA-5566). 00

34. A virally-immortalized human primary hepatocyte cell line Eal C-35 (ATCC 00 PTA-5565). A method of using the immortalized hepatocyte of claim 1 to assess the effects of a chemical entity on the liver.

36. The method of claim 35, wherein said chemical entity is a drug candidate.

37. The method of claim 36, wherein said hepatocyte retains hepatic function.

38. The method of claim 37, wherein said hepatic function comprises the ability to express hepatic enzyme activity.

39. The method of claim 38, wherein said hepatic enzyme activity comprises cytochrome P450 (CYP) enzymatic activity. The method of claim 39, wherein said immortalized hepatocyte is selected from the group consisting of the EalC-35 cell line (ATCC PTA-5565) and the Fa2N-4 cell line (ATCC PTA-5566).

41. A method of using the immortalized hepatocyte of claim 1 to assess enzyme induction.

42. The method of claim 41, wherein said hepatocyte retains hepatic function.

43. The method of claim 42, wherein said hepatic function comprises the ability to express hepatic enzyme activity. 00 44. The method of claim 43, wherein said hepatic enzyme activity comprises O 0 cytochrome P450 (CYP) enzymatic activity. The method of claim 44, wherein said immortalized hepatocyte is selected O Sfrom the group consisting of the EalC-35 cell line (ATCC PTA-5565) and the Fa2N-4 cell line (ATCC PTA-5566).

46. A method of using the immortalized hepatocyte of claim 1 to assess cellular 00 toxicity. 0, 47. The method of claim 46, wherein said hepatocyte retains hepatic function. O0

48. The method of claim 47, wherein said hepatic function comprises the ability to express hepatic enzyme activity.

49. The method of claim 48, wherein said hepatic enzyme activity comprises cytochrome P450 (CYP) enzymatic activity. The method of claim 49, wherein said immortalized hepatocyte is selected from the group consisting of the EalC-35 cell line (ATCC PTA-5565) and the Fa2N-4 cell line (ATCC PTA-5566).

51. A method of using the immortalized hepatocyte of claim 1 to assess the effect of a liver on a chemical entity.

52. The method of claim 51, wherein said hepatocyte retains hepatic function.

53. The method of claim 52, wherein said hepatic function comprises the ability to express hepatic enzyme activity.

54. The method of claim 53, wherein said hepatic enzyme activity comprises cytochrome P450 (CYP) enzymatic activity. The method of claim 54, wherein said immortalized hepatocyte is selected from the group consisting of the EalC-35 cell line (ATCC PTA-5565) and the Fa2N-4 cell line (ATCC PTA-5566). OO 56. The method of claim 51, wherein said liver effect on the chemical entity O Scomprises drug metabolism. S57. The method of claim 56, wherein said drug metabolism is measured by the O O formation of an acetaminophen conjugate.

58. A method using the immortalized hepatocytes of claim 1 to perform a S procedure selected from the group consisting of: 00 studies of malignant transformation by chemical, physical and viral O, agents, and transferred genes including oncogenes and high molecular Sweight genomic DNA from tumors, using standard assays such as anchorage independent growth or tumor formation in athymic nude mice; use of cells altered by transfer of oncogenes to screen for potential chemotherapeutic agents; studies of cellular biochemistry, including changes in intracellular pH and calcium levels, as correlated with cell growth and action of exogenous agents; studies of cellular responses to growth factors and production of growth factors; studies of intracellular communication; characterization of cell surface antigens; cell-cell hybrid studies for identification of tumor suppressor activity; identification of novel genes; growth of replicating hepatitis virus (as HBV, HCV, non-A non- B, HAV and other livertropic virus, CMV); 00 (10) identification of new drugs to treat hepatitis C virus (HCV) infection; O (11) expanding of cells for liver transplant and liver function assist devices, both implanted and extracorporeal; O S(12) studies of liver parasites; (13) studies of liver diseases; (14) identification of potential therapeutic drugs; 00 identification of new drug targets; 0, (16) identification of chemical and biological agents that induce terminal 0differentiation; (17) studies of the metabolism of carcinogens and other xenobiotics; (18) studies of DNA mutagenesis; (19) studies of chromosome damaging agents; studies of cytotoxicity of drugs, chemical entities, carcinogens, and xenobiotics; (21) production of hepatocyte-derived proteins; and (22) use of recombinant DNA expression vectors to produce proteins of interest.