Method of improving cell proliferation of pancreatic progenitor cells in a pancreatic cell culture
The invention relates to the discovery that the proliferation and survival of pancreatic progenitor cells can be enhanced by contacting the cells with, (1) a caspase inhibitor sufficient to reduce apoptosis in the pancreatic endocrine cells; and, (2) a growth factor in an amount sufficient to increase the level of activated Akt in the pancreatic endocrine cells.
1. A method of improving insulin or glucagon production in mature pancreatic endocrine cells in a pancreatic cell culture comprising
contacting pancreatic endocrine cells with (1) an exogenous caspase inhibitor in an amount sufficient to reduce apoptosis in the pancreatic endocrine cells; and (2) at least one exogenous growth factor in an amount sufficient to increase the level of activated Akt in the pancreatic endocrine cells; and
differentiating the pancreatic endocrine cells contacted with (1) and (2) into mature pancreatic endocrine cells that express insulin and/or glucagon at a synergistically higher level than differentiated pancreatic endocrine cells contacted only with (1) or (2), wherein glucagon and/or insulin are as measured by qPCR analysis of insulin mRNA or glucagon mRNA, respectively, and wherein the qPCR results are as displayed as the ratio of insulin mRNA to β-actin mRNA, or glucagon mRNA to actin mRNA, respectively.
2. The method of claim 1 , wherein the pancreatic endocrine cells are insulin producing aggregates.
3. The method of claim 1 wherein the caspase inhibitor is selected from the group consisting of: Q-VD-OPH, Z-VAD (OMe)-FMK, Ac-VAD-CHO, Boc-D-FMK, BACMK, BI-9B12, Ac-LDESD-CHO, and DEVD-CHO CPP32/Apopain Inhibitor.
4. The method of claim 1 , wherein the concentration of caspase inhibitor is from about 1 μm to about 100 μm.
5. The method of claim 1 , wherein the caspase inhibitor is an irreversible pan caspase inhibitor, selected from the group consisting of Q-VD-OPH and Z-VAD (OMe)-FMK.
6. The method of claim 5 , wherein the caspase inhibitor is Q-VD-OPH.
7. The method of claim 1 , wherein the growth factor is selected from the group consisting of EGF, IGF-I, IGF-II, heregulin, and PDGF-BB.
8. The method of claim 1 , wherein the growth factor is PDGF-BB and one or more members of the group consisting of IGF-I and IGF-II.
9. The method of claim 8 , wherein the concentration of each growth factor is from about 10 ng/ml to about 100 ng/ml of culture medium.
10. The method of claim 1 , wherein the pancreatic endocrine cells are progenitor pancreatic endocrine cells.