IP Library Granted Patent US 8,546,101
Granted Patent B2
US 8,546,101 · App. 13/021,497 · Granted Oct 1, 2013

Compound screening using chondrocytes derived from primate pluripotent stem cells

Inventor: R. Scott Thies (Pleasanton, CA)
Assignee: Geron Corporation
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Quick Facts
Patent No.
US 8,546,101
App. No.
13/021,497
Granted
Oct 1, 2013
Kind
B2
Abstract

This invention provides a system for obtaining cells of the chondrocyte lineage by differentiating primate pluripotent stem cells. The process involves culturing the cells as a micromass or other aggregate form in a cocktail of differentiation agents that facilitates outgrowth of the desired cell type. Progeny are capable of synthesizing Type II collagen or aggrecan, or other products that are characteristic of the chondrocyte lineage. Chondrocytes and chondrocyte precursor cells obtained according to this disclosure are suitable for use in both research and clinical therapy.

Claims (30)

1. A method of screening a compound for an effect on cultured chondrocytes, comprising:

a) providing primate pluripotent stem cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81;

b) culturing the primate pluripotent stem cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81 in a medium comprising one or more of transforming growth factor (TGF), fibroblast growth factor (FGF), growth differentiation factor (GDF), bone morphogenic protein (BMP), hedgehog protein, L-ascorbic acid and para-thyroid hormone related protein to produce cultured chondrocytes;

c) contacting the cultured chondrocytes with the compound; and

d) observing a change in the cultured chondrocytes.

2. The method of claim 1 , wherein the compound is a peptide.

3. The method of claim 1 , wherein the compound is an oligonucleotide.

4. The method of claim 1 , wherein the compound is a toxin.

5. The method of claim 1 , wherein the compound is a small molecule.

6. The method of claim 1 , wherein the compound is a solvent.

7. The method of claim 1 , wherein the cultured chondrocytes have chromosomal DNA that is at least 99.6% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

8. The method of claim 1 , wherein the cultured chondrocytes have chromosomal DNA that is at least 99.7% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

9. The method of claim 1 , wherein the cultured chondrocytes have chromosomal DNA that is at least 99.8% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

10. The method of claim 1 , wherein the cultured chondrocytes have chromosomal DNA that is at least 99.9% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

11. The method of claim 1 , wherein the cultured chondrocytes have chromosomal DNA that is genetically identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

12. A method of screening a compound for an effect on cultured cells expressing collagen type II and/or aggrecan chondrocytes, comprising:

a) providing primate pluripotent stem cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81;

b) culturing the primate pluripotent stem cells which express SSEA3, SSEA4,Tra-1-60 and Tra-1-81 in a medium comprising one or more of transforming growth factor (TGF), fibroblast growth factor (FGF), growth differentiation factor (GDF), bone morphogenic protein (BMP), hedgehog protein, L-ascorbic acid and para-thyroid hormone related protein to produce cultured cells expressing collagen type II and/or aggrecan;

c) contacting the cultured cells expressing collagen type II and/or aggrecan with the compound; and

d) observing a change in the cultured cells expressing collagen type II and/or aggrecan.

13. The method of claim 12 , wherein the compound is a peptide.

14. The method of claim 12 , wherein the compound is an oligonucleotide.

15. The method of claim 12 , wherein the compound is a toxin.

16. The method of claim 12 , wherein the compound is a small molecule.

17. The method of claim 12 , wherein the compound is a solvent.

18. The method of claim 12 , wherein the cultured collagen type II expressing chondrocytes have chromosomal DNA that is at least 99.6% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

19. The method of claim 12 , wherein the cultured collagen type II expressing chondrocytes have chromosomal DNA that is at least 99.7% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

20. The method of claim 12 , wherein the cultured collagen type II expressing chondrocytes have chromosomal DNA that is at least 99.8% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

21. The method of claim 12 , wherein the cultured collagen type II expressing chondrocytes have chromosomal DNA that is at least 99.9% identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

22. The method of claim 12 , wherein the cultured collagen type II expressing chondrocytes have chromosomal DNA that is identical to the chromosomal DNA of an established line of cells which express SSEA3, SSEA4, Tra-1-60 and Tra-1-81.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2013
From: GERON CORPORATION
To: ASTERIAS BIOTHERAPEUTICS, INC.
Reel/Frame 031620/0567 →
Continuity (4)
Division 11345878 · Feb 1, 2006
Continuation 10313740 · Dec 6, 2002
Provisional Application 60339043 · Dec 7, 2001
Related Publication 20110129867A1 · Jun 2, 2011