PDX1-expressing dorsal and ventral foregut endoderm
Disclosed herein are cell cultures comprising dorsal and/or ventral PDX1-positive foregut endoderm cells and methods of producing the same. Also disclosed herein are cell populations comprising substantially purified dorsal and/or ventral PDX1-positive foregut endoderm cells as well as methods for enriching, isolating and purifying dorsal and/or ventral PDX1-positive foregut endoderm cells from other cell types. Methods of identifying differentiation factors capable of promoting the differentiation of dorsal and/or ventral PDX1-positive foregut endoderm cells, are also disclosed.
1. An in vitro cell culture comprising human definitive endoderm cells, human pancreatic-duodenal homeobox factor-1 (PDX1) positive foregut endoderm cells, and a medium comprising an effective amount of a TGFβ superfamily member and an effective amount of a retinoid, wherein the effective amount of a TGFβ superfamily member and retinoid promote differentiation of definitive endoderm cells to PDX1-positive foregut endoderm cells, wherein the TGFβ superfamily member is activin A and wherein the retinoid is retinoic acid.
2. The cell culture of claim 1 , wherein at least a portion of the PDX1 positive foregut endoderm cells express the PDX1 protein.
3. The cell culture of claim 1 , wherein at least 10% of human cells in said in vitro culture are PDX1-positive foregut endoderm cells.
4. The cell culture of claim 1 , wherein at least 60% of human cells in said in vitro culture are PDX1-positive foregut endoderm cells.
5. The cell culture of claim 1 , wherein at least 75% of human cells in said in vitro culture are PDX1-positive foregut endoderm cells.
6. The cell culture of claim 1 , wherein the PDX1-positive foregut endoderm cells are selected from the group consisting of PDX1-positive dorsally-biased endoderm cells and PDX1-positive ventrally-biased endoderm cells.
7. The cell culture of claim 1 , wherein the PDX1-positive foregut endoderm cells are PDX1-positive dorsally-biased foregut endoderm cells.
8. The cell culture of claim 1 , wherein said PDX1-positive endoderm cells are derived in vitro from human pluripotent cells.
9. The cell culture of claim 8 , wherein said human pluripotent cells do not form embryoid bodies prior to differentiation.
10. The cell culture of claim 1 , wherein activin A is provided at a concentration of least 25 ng/ml.
11. The cell culture of claim 10 , wherein the retinoic acid is provided at a concentration of about 2 μM.