Differntiation method for production of glial cell population
The present invention provides methods for generating oligodendrocyte progenitor cells from pluripotent cells, as well as methods for sustaining these oligodendrocyte progenitor cells in relatively pure cultures for long periods of time. The present invention also provides methods for further differentiating these oligodendrocyte progenitor cells into various glial cells.
1. A composition comprising mammalian oligodendrocyte progenitor cells, the oligodendrocyte progenitor cells generated by providing a pluripotent cell; inducing development of the pluripotent cell into neuroectoderm by culturing the pluripotent cell in the presence of one or more inhibitors of an activin-nodal pathway and one or more inhibitors of a bone morphogenetic protein pathway; inducing development of patterned neuroectoderm by culturing the neuroectoderm in the presence of two or more of sonic hedgehog, retinoic acid and noggin; and inducing development of oligodendrocyte progenitor cells by culturing the patterned neuroectoderm cells in the presence of one or more of a fibroblast growth factor, a platelet-derived growth factor and sonic hedgehog.
2. The composition of claim 1 , further comprising neurons or neuron precursors.
3. A composition comprising mammalian oligodendrocyte progenitor cells, the oligodendrocyte progenitor cells generated by providing a pluripotent cell; inducing development of the pluripotent cell into neuroectoderm by culturing the pluripotent cell in the presence of one or more inhibitors of an activin-nodal pathway and one or more inhibitors of a bone morphogenetic protein pathway; inducing development of patterned neuroectoderm by culturing the neuroectoderm in the presence of two or more of sonic hedgehog, retinoic acid and noggin; inducing development of oligodendrocyte progenitor cells by culturing the patterned neuroectoderm cells in the presence of one or more of a fibroblast growth factor, a platelet-derived growth factor and sonic hedgehog; and culturing the oligodendrocyte progenitor cells in the presence of an activator of Wnt-13-catenin signaling, wherein the oligodendrocyte progenitor cells remain in a progenitor cell state.
4. The composition of claim 3 , further comprising neurons or neuron precursors.
5. The composition of claim 1 , wherein the oligodendrocyte progenitor cells can be expanded for at least eight passages.
6. The composition of claim 3 , wherein the oligodendrocyte progenitor cells can be expanded for at least eight passages.
7. A method of treating a medical condition of the central nervous system (CNS) in a subject comprising administering to the subject a therapeutically effective amount of the composition of claim 1 .
8. A method of generating the composition of claim 3 , comprising:
providing a pluripotent cell;
inducing development of the pluripotent cell into neuroectoderm by culturing the pluripotent cell in the presence of one of more inhibitors of an activin-nodal pathway and one or more inhibitors of a bone morphogenetic protein pathway;
inducing development of patterned neuroectoderm by culturing the neuroectoderm in the presence of two or more of sonic hedgehog, retinoic acid and noggin;
inducing development of oligodendrocyte progenitor cells by culturing the patterned neuroectoderm cells in the presence of one or more of a fibroblast growth factor, a platelet-derived growth factor and sonic hedgehog; and
culturing the oligodendrocyte progenitor cells in the presence of an activator of Wnt-β-catenin signaling and maintaining the oligodendrocyte progenitor cells in cell culture.
9. The method of claim 8 , wherein the activator of Wnt-β-catenin signaling is a GSK313 inhibitor.
10. The method of claim 9 , wherein the GSK313 inhibitor is CHIR99021.
11. A method of treating a medical condition of the central nervous system (CNS) in a subject comprising administering to the subject a therapeutically effective amount of the composition of claim 3 .
12. The method of claim 8 , further comprising culturing the oligodendrocyte progenitor cells in the absence of FGF and PDGF and in the presence of the thyroid hormone T3.