Differentiation of human embryonic stem cells
The present invention provides methods to promote the differentiation of pluripotent stem cells into insulin producing cells. In particular, the present invention provides a method to produce a population of cells expressing markers characteristic of the pancreatic endoderm lineage, wherein greater than 50% of the cells in the population co-express PDX1 and NKX6.1.
1. A cell culture comprising:
a medium supplemented with ALK5 inhibitor II and a protein kinase C activator;
human definitive endoderm cells; and
a population of human cells expressing markers characteristic of the pancreatic endoderm lineage,
wherein the presence of ALK5 inhibitor II and the protein kinase C activator in the culture increases the percentage of pancreatic endoderm cells that co-express PDX1 and NKX6.1, and results in a culture wherein greater than 60% of the cells in the population are pancreatic endoderm cells co-expressing PDX1 and NKX6.1,
wherein the human definitive endoderm cells are derived from established lines of human pluripotent cells, and
wherein cells in the isolated PDX1 and NKX6.1 co-expressing population express CDX2.
2. The cell culture of claim 1 wherein greater than 70% of the cells in the population co-express PDX1 and NKX6.1.
3. The cell culture of claim 1 wherein greater than 80% of the cells in the population co-express PDX1 and NKX6.1.
4. The cell culture of claim 1 wherein greater than 90% of the cells in the population co-express PDX1 and NKX6.1.
5. The cell culture of claim 1 , wherein cells in the cell population express ISL1 and/or NEUROD1.
6. The cell culture of claim 1 , wherein the protein kinase C activator is selected from the group consisting of (2S, 5S)-(E, E)-8-(5-(4-(Trifluoromethyl)phenyl)-2,4-pentadiemoylamino) benzolactam (TPB), phorbol-12-myristate-13-acetate (PMA), and phorbol-12,13-dibutyrate (PDBu).
7. A cell culture comprising:
a medium supplemented with ALK5 inhibitor II and a protein kinase C activator;
human definitive endoderm cells; and
a population of human cells expressing markers characteristic of the pancreatic endoderm lineage,
wherein the presence of ALK5 inhibitor II and the protein kinase C activator in the culture increases the percentage of pancreatic endoderm cells that co-express PDX1 and NKX6.1, and results in a culture wherein greater than 60% of the cells in the population are pancreatic endoderm cells co-expressing PDX1 and NKX6.1,
wherein the human definitive endoderm cells are derived from established lines of human pluripotent cells, and
wherein the PDX1 and NKX6.1 co-expressing cells in the isolated population differentiate into insulin secreting cells in vivo.
8. The cell culture of claim 7 , wherein cells in the cell population express ISL1 and/or NEUROD1.
9. The cell culture of claim 7 , wherein greater than 70% of the cells in the population co-express PDX1 and NKX6.1.
10. The cell culture of claim 7 , wherein greater than 80% of the cells in the population co-express PDX1 and NKX6.1.
11. The cell culture of claim 7 , wherein greater than 90% of the cells in the population co-express PDX1 and NKX6.1.
12. The cell culture of claim 7 , wherein the protein kinase C activator is selected from the group consisting of (2S, 5S)-(E, E)-8-(5-(4-(Trifluoromethyl)phenyl)-2,4-pentadiemoylamino) benzolactam (TPB), phorbol-12-myristate-13-acetate (PMA), and phorbol-12,13-dibutyrate (PDBu).
13. The cell culture of claim 1 , wherein the cells expressing markers characteristic of the pancreatic endoderm lineage are pancreatic endoderm cells.
14. The cell culture of claim 7 , wherein the cells expressing markers characteristic of the pancreatic endoderm lineage are pancreatic endoderm cells.
15. A cell culture comprising:
a medium supplemented with ALK5 inhibitor II and a protein kinase C activator;
human definitive endoderm cells; and
a population comprising pancreatic endoderm cells,
wherein the presence of ALK5 inhibitor II and the protein kinase C activator in the culture increases the percentage of pancreatic endoderm cells that co-express PDX1 and NKX6.1, and results in a culture wherein greater than 90% of the cells in the population are pancreatic endoderm cells co-expressing PDX1 and NKX6.1, and
wherein the human definitive endoderm cells are derived from established lines of human pluripotent cells.
16. The cell culture of claim 1 , wherein cells in the cell population express NEUROD1.
17. The cell culture of claim 1 , wherein the cells are obtained by culturing a population of cells expressing markers characteristic of the definitive endoderm lineage in a medium supplemented with a protein kinase C activator and lacking FGF10.
18. The cell culture of claim 7 , wherein cells in the cell population express NEUROD1.
19. The cell culture of claim 1 , wherein the cells are obtainable by culturing a population of cells expressing markers characteristic of the definitive endoderm lineage in a medium supplemented with a protein kinase C activator and lacking FGF10.
20. A cell culture comprising:
a medium supplemented with (2S, 5S)-(E, E)-8-(5-(4-(Trifluoromethyl)phenyl)-2,4-pentadiemoylamino) benzolactam (TPB);
human definitive endoderm cells; and
a population of human cells expressing markers characteristic of the pancreatic endoderm lineage,
wherein the presence of TPB in the culture increases the percentage of pancreatic endoderm cells that co-express PDX1 and NKX6.1, and results in a culture wherein greater than 60% of the cells in the population are pancreatic endoderm cells co-expressing PDX1 and NKX6.1,
wherein the human definitive endoderm cells are derived from established lines of human pluripotent cells, and
wherein cells in the isolated population express CDX2.
21. The cell culture of claim 1 , wherein the culturing of the first population of cells expressing markers characteristic of the definitive endoderm does not require purification.
22. The cell culture of claim 7 , wherein the culturing of the first population of cells expressing markers characteristic of the definitive endoderm does not require purification.
23. The cell culture of claim 15 , wherein the culturing of the first population of cells expressing markers characteristic of the definitive endoderm does not require purification.
24. The cell culture of claim 20 , wherein the culturing of the first population of cells expressing markers characteristic of the definitive endoderm does not require purification.