Target populations of oligodendrocyte precursor cells and methods of making and using same
This application provides for enriched target populations oligodendrocyte precursor cells (OPCs) that can differentiate into oligodendrocytes. The target OPCs may be expanded and optionally subjected to conditions to induce their differentiation into oligodendrocytes. The target OPCs and their progeny are useful for the treatment of disease associated with demyelination of central nervous system axons.
1. A method of producing a population enriched for oligodendrocyte precursor cells comprising:
(a) contacting neural or neural derived cells comprising one or more multipotent central nervous system stem cell with an antibody that specifically binds to PDGFRα; and
(b) selecting said neural or neural derived cells that are PDGFRα hi , wherein the selected cells are enriched for oligodendrocyte precursor cells as compared with the neural or neural derived cells.
2. The method of claim 1 , wherein said neural or neural derived cells are obtained from a neurosphere culture or an adherent culture.
3. The method of claim 1 , wherein the method further comprises the step of eliminating those cells that are PDGFRα lo/med .
4. The method of claim 1 , wherein the method further comprises the step of eliminating cells that are CD105 + .
5. The method of claim 4 , wherein the oligodendrocyte precursor cells are PSA-NCAM lo/− .
6. The method of claim 4 , wherein the oligodendrocyte precursor cells are A2B5 lo/− .
7. The method of claim 4 , wherein the oligodendrocyte precursor cells are CD133 + .
8. The method of claim 7 , wherein the oligodendrocyte precursor cells are A2B5 lo/− .
9. The method of claim 8 , wherein the oligodendrocyte precursor cells are PSA-NCAM lo/− .
10. The method of claim 1 , wherein the oligodendrocyte precursor cells are CD105 − .
11. The method of claim 1 , wherein the oligodendrocyte precursor cells are PSA-NCAM lo/− .
12. The method of claim 1 , wherein the oligodendrocyte precursor cells are A2B5 lo/− .
13. The method of claim 1 , wherein the oligodendrocyte precursor cells are CD133 + .