Methods for identifying factors for differentiating definitive endoderm
Disclosed herein are methods of identifying one or more differentiation factors that are useful for differentiating cells in a cell population comprising definitive endoderm cells into cells which are capable of forming tissues and/or organs that are derived from the gut tube.
1. A method of identifying a factor that promotes the differentiation of human definitive endoderm cells, said method comprising the steps of:
obtaining a human cell population comprising human definitive endoderm cells, wherein said human definitive endoderm cells comprise at least 10% of the human cells in said cell population;
providing a candidate differentiation factor to said cell population;
determining expression of a marker of a cell differentiated from definitive endoderm in said cell population at a first time point;
determining expression of the same marker in said cell population at a second time point, wherein said second time point is subsequent to said first time point and wherein said second time point is subsequent to providing said cell population with said candidate differentiation factor; and
determining if expression of the marker in said cell population at said second time point is increased as compared to the expression of the marker in said definitive endoderm cell population at said first time point, wherein an increase in expression of said marker in said cell population indicates that said candidate differentiation factor promotes the differentiation of said human definitive endoderm cells.
2. The method of claim 1 , wherein human feeder cells are present in said cell population and wherein at least 10% of the human cells other than said feeder cells are definitive endoderm cells.
3. The method of claim 1 , wherein said human definitive endoderm cells comprise at least 90% of the human cells in said cell population.
4. The method of claim 1 , wherein said human feeder cells are present in said cell population and wherein at least 90% of the human cells other than said feeder cells are definitive endoderm cells.
5. The method of claim 1 , wherein said marker is selected from the group consisting of pancreatic-duodenal homeobox factor-1 (PDX1), homeobox A13 (HOXA13) and homeobox C6 (HOXC6) in response to said candidate differentiation factor.
6. The method of claim 1 , wherein said marker is selected from the group consisting of albumin, prospero-related homeobox 1 (PROX1) and hepatocyte specific antigen (HSA) in response to said candidate differentiation factor.
7. The method of claim 1 , wherein said marker is thyroid transcription factor 1 (TITF1) in response to said candidate differentiation factor.
8. The method of claim 1 , wherein said marker is selected from the group consisting of villin and caudal type homeobox transcription factor 2 (CDX2)) in response to said candidate differentiation factor.
9. The method of claim 1 , wherein said first time point is prior to providing said candidate differentiation factor to said cell population.
10. The method of claim 1 , wherein said first time point is at approximately the same time as providing said candidate differentiation factor to said cell population.
11. The method of claim 1 , wherein said first time point is subsequent to providing said candidate differentiation factor to said cell population.
12. The method of claim 1 , wherein expression of said marker is increased.
13. The method of claim 1 , wherein expression of said marker is determined by quantitative polymerase chain reaction (Q-PCR).
14. The method of claim 1 , wherein expression of said marker is determined by immunocytochemistry.
15. The method of claim 1 , wherein said candidate differentiation factor comprises a small molecule.
16. The method of claim 1 , wherein said candidate differentiation factor comprises a retinoid.
17. The method of claim 1 , wherein said candidate differentiation factor comprises retinoic acid.
18. The method of claim 1 , wherein said candidate differentiation factor comprises a polypeptide.
19. The method of claim 1 , wherein said candidate differentiation factor comprises a growth factor.
20. The method of claim 1 , wherein said candidate differentiation factor comprises FGF-10.
21. The method of claim 1 , wherein said candidate differentiation factor comprises FGF-2.
22. The method of claim 1 , wherein said candidate differentiation factor comprises Wnt3B.
23. The method of claim 1 , wherein said candidate differentiation factor is not a foregut differentiation factor.
24. The method of claim 1 , wherein said candidate differentiation factor is not a retinoid.
25. The method of claim 1 , wherein said candidate differentiation factor is not retinoic acid.
26. The method of claim 1 , wherein said candidate differentiation factor is provided to said cell population at a concentration of between 0.1 ng/ml to 10 mg/ml.
27. The method of claim 1 , wherein said candidate differentiation factor is provided to said cell population at a concentration of between 1 ng/ml to 1 mg/ml.
28. The method of claim 1 , wherein said candidate differentiation factor is provided to said cell population at a concentration of between 10 ng/ml to 100 μg/ml.
29. The method of claim 1 , wherein said candidate differentiation factor is provided to said cell population at a concentration of between 100 ng/ml to 10 μg/ml.
30. The method of claim 1 , wherein said candidate differentiation factor is provided to said cell population at a concentration of 1 μg/ml.
31. The method of claim 1 , wherein said candidate differentiation factor is provided to said cell population at a concentration of 100 ng/ml.