Amnion-Derived Cell Compositions, Methods of Making and Uses Thereof

• US 20100028306A1
• Filed: 03/29/2006
• Published: 02/04/2010
• Est. Priority Date: 03/31/2005
• Status: Abandoned Application

• Current Assignee: Stemnion, Inc.
• Original Assignee: Stemnion, Inc.
• Inventors: Smith, Charlotte A., Clarke, Diana L., Marshall, Vivienne S., Banas, Richard A.
• Application Number:
  US11/887,291
• Publication Number:
  US 20100028306A1
• Time in Patent Office: Days
• US Class Current: 424/93.700
• 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: C12N 2501/11 Epidermal growth factor [EGF]
• CPC Class Codes: C12N 2502/1323 Adult fibroblasts
• CPC Class Codes: C12N 2506/02 from embryonic cells
• CPC Class Codes: C12N 2531/00 Microcarriers
• CPC Class Codes: C12N 5/0605 Cells from extra-embryonic tissues, e.g. placenta, amnion, yolk sac, Wharton's jelly
• CPC Class Codes: C12N 5/0676 Pancreatic cells
• CPC Class Codes: C12N 5/0678 Stem cells; Progenitor cells; Precursor cells

Abstract

The invention is directed to substantially purified amnion-derived cell populations, compositions comprising the substantially purified amnion-derived cell populations, and to methods of creating such substantially purified amnion-derived cell populations, as well as methods of use. The invention is further directed to antibodies, in particular, monoclonal antibodies, that bind to amnion-derived cells or, alternatively, to one or more amnion-derived cell surface protein markers. The invention is further directed to methods for producing the antibodies, methods for using the antibodies, and kits comprising the antibodies.

Claims

1. (canceled)

2. (canceled)

3. (canceled)

4. (canceled)

5. (canceled)

6. (canceled)

7. (canceled)

8. (canceled)

9. (canceled)

10. (canceled)

11. (canceled)

12. (canceled)

13. (canceled)

14. (canceled)

15. (canceled)

16. (canceled)

17. A population of early pancreatic progenitor cells differentiated from a substantially purified population of amnion-derived cells that is negative for the expression of the protein markers CD90 and CD117, wherein the early pancreatic progenitor cells express a pancreatic progenitor cell marker protein.

18. The population of claim 17, wherein the progenitor cell marker is PDX1 protein and wherein the cells further optionally express any one or more of the protein markers selected from the group consisting of Foxa2, p48, Hblx9, Ngn3, NKx2.2, Nkx6. 1, insulin and islet-1.

19. The population of claim 18, wherein the PDX1 protein is expressed in the nucleus.

20. The population of claim 17 wherein the cells are differentiated pancreatic progenitor cells.

21. The population of claim 20, wherein the differentiated progenitor cells express any one or more of the protein markers selected from the group consisting of PDX1, insulin, C-peptide, somatostatin, pancreatic polypeptide, and glucagon.

22. The population of claim 20 wherein the differentiated pancreatic progenitor cells are islet-like cells.

23. The population of claim 22, wherein the islet-like cells are functional alpha, beta, delta or phi cells.

24. The population of claim 23, wherein functionality of the islet-like cells is incremental glucose-dependent insulin secretion.

25. The population of claim 18, wherein the cells form spheroids.

26. The population or composition of claim 25, wherein the spheroids form buds.

27. The population of claim 26, wherein the buds express PDX1 protein.

28. The population of claim 27, wherein the PDX1 protein is expressed in the nucleus.

29. The population of claim 20, which comprises one or more mammalian islet cells.

30. The population of claim 29, wherein the mammalian islet cells are human cells.

41. A pharmaceutical composition comprising an effective amount of the population of claim 17 and a carrier.

46. The population of claim 29 wherein the islet cells are islet progenitor cells.

47. The population of claim 46 wherein the islet progenitor cells are embryonic islet progenitor cells.

48. An in vivo method for promoting the generation of islet progenitor cells and/or islet cells in a subject comprising:

a) transplanting the population of claim 17 into the pancreas of the subject;

b) introducing factors into the pancreas of the subject; and

c) allowing the introduced factors to promote generation of islet progenitor cells and/or islet cells from the transplanted population.

31. (canceled)

33. (canceled)

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40. (canceled)

42. An islet progenitor cell population differentiated from amnion-derived cells that are negative for the expression of the protein markers CD90 and CD117, wherein the islet progenitor cell population expresses at least one early pancreatic determination gene.

32. The population of claim 43, wherein the cells have the identifying characteristics of endoderm, wherein the identifying characteristics of endoderm are expression of HNF1α

, HNF1β

, HNF4α

, HNF6, Foxa2 and PDX1 proteins and wherein the cells further optionally expressing any one or more of the protein markers Sox17, Cerberus, Hesx1, LeftyA, Otx1 or Otx2.

43. The islet progenitor cell population of claim 42, wherein the early pancreatic determination gene is PDX1.

44. A cell population differentiated from amnion-derived cells that are negative for the expression of the protein markers CD90 and CD117, wherein the cell population has the identifying characteristics of endoderm.

45. The cell population of claim 44 that is a pancreatic progenitor cell population.

49. An in vivo method for promoting the differentiation of amnion-derived cells into pancreatic cells comprising

(a) introducing factors to the population of amnion-derived cells in vitro;

and

(b) subsequently transplanting the amnion-derived cells into the pancreas of a subject.