Induction of hepatocyte proliferation in vitro by inhibition of cell cycle inhibitors

• US 20050148073A1
• Filed: 09/20/2004
• Published: 07/07/2005
• Est. Priority Date: 03/20/2002
• Status: Abandoned Application

• Current Assignee: Regents of The University of Minnesota (University of Minnesota)
• Original Assignee: Regents of The University of Minnesota (University of Minnesota)
• Inventors: Hansen, Linda K., Fassett, John T.
• Application Number:
  US10/945,854
• Publication Number:
  US 20050148073A1
• Time in Patent Office: Days
• US Class Current: 435/370
• CPC Class Codes: A61K 35/12 Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells vaccines or medicinal preparations containing antigens or antibodies A61K39/00
• CPC Class Codes: C07H 19/16 Purine radicals
• CPC Class Codes: C12N 2500/90 Serum-free medium, which may still contain naturally-sourced components
• CPC Class Codes: C12N 2501/11 Epidermal growth factor [EGF]
• CPC Class Codes: C12N 2501/70 Enzymes
• CPC Class Codes: C12N 2503/02 Drug screening
• CPC Class Codes: C12N 2506/03 from non-embryonic pluripotent stem cells
• CPC Class Codes: C12N 2533/52 Fibronectin; Laminin
• CPC Class Codes: C12N 2533/54 Collagen; Gelatin
• CPC Class Codes: C12N 2533/90 Substrates of biological origin, e.g. extracellular matrix, decellularised tissue
• CPC Class Codes: C12N 5/067 Hepatocytes
• CPC Class Codes: G01N 33/5067 Liver cells

Abstract

The present invention provides methods of inducing proliferative and differentiative mammalian hepatocytes, or survival of differentiative mammalian hepatocytes, in vitro comprising contacting the hepatocytes with protein kinase A (PKA) inhibitor.

Claims

1. A method of inducing proliferative and differentiative mammalian hepatocytes in vitro comprising (a) contacting the hepatocytes with protein kinase A (PKA) inhibitor.

2. The method of claim 1, wherein the protein kinase A inhibitor is a nucleotide or nucleoside derivative of formula I:

3. The method of claim 1, wherein the protein kinase A inhibitor is a peptide having SEQ ID NO:

2, Xaa-Arg-Arg-Xaa-Ala-Xaa, wherein Xaa is any amino acid.

4. The method of claim 1, wherein the protein kinase A inhibitor is a peptide or polypeptide with SEQ ID NO:

3, SEQ ID NO;

4, SEQ ID NO;

5, SEQ ID NO;

6, SEQ ID NO;

7, SEQ ID NO;

8, SEQ ID NO;

9, or SEQ ID NO;

10.

5. The method of claim 1, wherein the protein kinase A inhibitor is N-[2-((p-bromocinnamyl)amino)ethyl]-5-isoquinolinesulfonamide.

6. The method of claim 1, wherein the protein kinase A inhibitor is:

7. The method of claim 1, wherein the protein kinase A inhibitor is:

8. The method of claim 1, wherein the protein kinase A inhibitor is:

4,4′

,5,5′

,6,6′

-hexahydroxydiphenic acid 2,6,2′

,6′

-dilactone, 1-(5-Isoquinolinesulfonyl)-2-methylpiperazine, N-[2-(methylamino)ethyl]-5-isoquinolinesulfonamide, N-(2-aminoethyl)-5-isoquinolinesulfonamide, or (5-isoquinolinesulfonyl)piperazine.

9. The method of claim 1, wherein the hepatocytes are primary hepatocytes.

10. The method of claim 1, wherein the hepatocytes are generated from stem cells.

11. The method of claim 1, comprising (b) growing the hepatocytes on a biocompatible support matrix.

12. The method of claim 11, wherein the support matrix is a collagen gel matrix.

13. The method of claim 11, wherein the support matrix is a collagen film.

14. The method of claim 11, wherein the solid substrate is a collagen gel sandwich.

15. The method of claim 11, further comprising (c) growing the hepatocytes in the absence of PKA inhibitor for an interval of time.

16. The method of claim 15, further comprising (d) repeating steps (a) and (b).

17. The method of claim 1, wherein the hepatocytes are of human origin.

18. The method of claim 1, wherein the hepatocytes are of porcine origin.

19. The method of claim 1, wherein the protein kinase A inhibitor is present at a concentration of 0. 1, 0.5, 1, 3, or 5 μ

M.

20. The method of claim 1, wherein the protein kinase A inhibitor is present at a concentration of about 1 to 3 μ

M.

21. A method of promoting survival of differentiative mammalian hepatocytes in vitro comprising contacting the hepatocytes with protein kinase A inhibitor.

22. A method of screening a compound for its effect on hepatocytes or a hepatocyte activity, comprising:

(a) combining the compound with a cell population obtained by treating hepatocytes with a protein kinase A;

(b) determining any change to cells in the population or their activity that results from being combined with the compound; and

(c) correlating the change with the effect of the compound on hepatocytes or a hepatocyte.

23. The method of claim 22, comprising determining whether the compound is toxic to cells in the population.

24. The method of claim 22, comprising determining whether the compound affects cell proliferation in the population or maintenance in culture of cells in the population.

25. The method of claim 22, comprising determining whether the compound changes enzyme activity or secretion.

26. The method of claim 25 comprising determining whether the compound changes activity of a hepatocyte Phase I metabolizing enzyme.

27. The method of claim 25, comprising determining whether the compound changes activity of a hepatocyte Phase II metabolizing enzyme.

28. The method of claim 25, comprising determining whether the compound changes cytochrome p450 expression or activity.

29. The method of claim 25, comprising determining whether the compound changes CYP3A3-5 activity, CYP2D activity, or CYP2C9 activity.

30. The method of claim 25, comprising determining whether the compound affects CYP1A1 or CYP1A2 activity.

31. The method of claim 22, comprising determining whether the compound affects the activity of 7-ethoxycoumarin O-de-ethylase, aloxyresorufin O-de-alkylase, coumarin 7-hydroxylase, p-nitrophenol hydroxylase, testosterone hydroxylation, UDP-glucuronyltransferase, glutathione S-transferase, gamma-glutamyl tranpeptidase, or glucose-6-phosphatase.

32. The method of claim 22, comprising determining whether the compound affects the synthesis of a plasma protein.

33. The method of claim 32, wherein the plasma protein is albumin, transferrin, alpha₁-antitrypsin, or alpha-fetoprotein.

34. The method of claim 22, comprising determining whether the compound affects gluconeogenesis, ureagenesis, bilirubin conjugation, or bile acid conjugation.

35. The method of claim 22, comprising determining whether the compound affects synthesis or secretion of cholesterol or lipoprotein, levels of glutathione, nucleoside phosphate metabolism, intracellular K²⁺ or Ca⁺ concentration, release of nuclear matrix proteins or oligonucleosomes, induction of apoptosis, or glycogen storage.

36. The method of claim 22, wherein the hepatocytes are human in origin.

37. The method of claim 22, wherein cells in the population have been genetically altered.

38. A bioartificial liver device comprising a proliferative and differentiative mammalian hepatocyte.

39. The bioartificial liver device of claim 38, further comprising a biocompatible support matrix.

40. The device of claim 39, wherein the support matrix is a collagen gel matrix.

41. The device of claim 39, wherein the support matrix is a collagen film.

42. The device of claim 39, wherein the support matrix is a collagen gel sandwich.

43. An artificial liver device comprising:

(a) a cell culture layer comprising cells from an isolated cell line of normal hepatocytes and a protein kinase A inhibitor, and

(b) a support matrix that provides means for fluid circulation across the cell culture layer.

44. The artificial liver device of claim 43, wherein the fluids are culture medium, plasma or blood.

45. A method of transplanting hepatocytes comprising:

(a) inducing a population of proliferative and differentiative mammalian hepatocytes in vitro comprising contacting the hepatocytes with protein kinase A inhibitor; and

(b) transplanting the population of hepatocytes.