Low oxygen tension enhances endothelial fate of human pluripotent stem cells
Low oxygen tension is a critical regulator of the developing or regenerating vasculature. The present invention is based on the determination that low oxygen tension during early stages of early vascular cell (EVC) derivation induces endothelial commitment and maturation of pluripotent stem cells. Inhibition of reactive oxygen species generation during the early stages of differentiation abrogates the endothelial inductive effects of the low oxygen environments. Methods of generating various types of cells from pluripotent stem cells (PSCs) are described, as well as compositions and methods of use thereof. In particular, generation of EVCs, bicellular vascular populations, early endothelial cells (ECs) and pericytes via culture in a low oxygen environment is described.
1. A method of generating early vascular cells (EVCs) comprising endothelial cells (ECs) and pericytes, comprising:
a) culturing pluripotent stem cells (PSCs) under hypoxic conditions of about 1-5% oxygen on a first two-dimensional culture substrate in a monolayer in a first growth medium for a time suitable to induce differentiation of the PSCs to generate EVCs;
b) differentiating the cells of a) under hypoxic conditions of about 1-5% oxygen on a second culture substrate in a second growth medium comprising a transforming growth factor-β(TGF-β) inhibitor and a vascular endothelial growth factor (VEGF) for a time suitable to induce differentiation of the cells of b) to generate a population of ECs expressing vascular endothelial cadherin and pericytes expressing platelet-derived growth factor receptor beta and neural/glial antigen 2 (NG2), thereby generating EVCs comprising ECs and pericytes.
2. The method of claim 1 , wherein the PSCs are human pluripotent stem cells (hPSCs) that are cultured on a two-dimensional substrate selected from a petri dish, a roller bottle, a flask or a three-dimensional substrate.
3. The method of claim 1 , wherein hypoxic conditions are about 5% oxygen.
4. The method of claim 1 , wherein the first two-dimensional culture substrate is selected from the group consisting of type I collagen, type IV collagen and fibronectin.
5. The method of claim 1 , wherein the ECs are surrounded by the pericytes.
6. The method of claim 1 , wherein the TGF-β inhibitor is SB431542.
7. The method of claim 1 , wherein the second growth medium comprises from about 1 to 25 μM TGF-β inhibitor.
8. The method of claim 1 , wherein the second growth medium comprises 10 μM SB431542.
9. The method of claim 1 , wherein the VEGF is VEGF-A.
10. The method of claim 1 , wherein the second growth medium comprises from about 10 to 80 ng/ml VEGF.
11. The method of claim 1 , wherein the second growth medium comprises 50 ng/ml VEGF.
12. The method of claim 1 , wherein the time suitable to induce differentiation in step a) is about 2 to 12 days.
13. The method of claim 1 , wherein the time suitable to induce differentiation in step b) is about 2 to 12 days.
14. A method of generating early vascular cells (EVCs) comprising endothelial cells (ECs) and pericytes, comprising:
a) culturing pluripotent stem cells (PSCs) under hypoxic conditions of about 1-5% oxygen on a first two-dimensional culture substrate in a monolayer in a first growth medium suitable to induce differentiation of the PSCs to generate EVCs;
b) differentiating the cells of a) under hypoxic conditions of about 1-5% oxygen on a second culture substrate in a second growth medium consisting essentially of a transforming growth factor-β(TGF-β) inhibitor and vascular endothelial growth factor (VEGF), thereby inducing differentiation of the cells of a) into a population of ECs expressing vascular endothelial cadherin and pericytes expressing platelet-derived growth factor receptor beta and neural/glial antigen 2 (NG2), thereby generating EVCs comprising ECs and pericytes.