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AssigneeCornell Research Foundation, Inc.
InventorsSteven A. Goldman, Su Wang
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The present invention is directed to a method of separating oligodendrocyte cells or progenitor cells thereof from a mixed population of cells. It comprises selecting a promoter which functions only in the oligodendrocyte cells or progenitor cells thereof, introducing a nucleic acid molecule encoding a fluorescent protein under control of that promoter into the mixed population cells, allowing the oligodendrocyte cells or progenitor cells thereof to express the fluorescent protein, and separating the fluorescent cells from the mixed population cells, where the separated cells are the oligodendrocyte cells or progenitor cells thereof. The invention also relates to the isolated and enriched human oligodendrocyte cells or progenitor cells thereof.
An enriched or purified preparation of human mitotic oligodendrocyte progenitor cells, wherein the majority of cells in the enriched or purified preparation differentiate into O4 positive oligodendrocytes, when cultured in PDGF, FGF2, and NT3, and further develop into galactocerebroside positive oligodendrocytes in the presence of 5% FBS/IGF-1, the mitotic oligodendrocyte progenitor cells are from a post-natal human, and a human cyclic nucleotide phosphodiesterase gene P2 promoter is transcriptionally active in the oligodendrocyte progenitor cells.
An enriched or purified preparation of human mitotic oligodendrocyte progenitor cells, wherein the majority of cells in the enriched or purified preparation differentiate into O4 positive oligodendrocytes, when cultured in PDGF, FGF2, and NT3, and further develop into galactocerebroside positive oligodendrocytes in the presence of 5% FBS/IGF-1, the mitotic oligodendroctye progenitor cells are from an adult human, and a human cyclic nucleotide phosphodiesterase gene P2 promoter is transcriptionally active in the oligodendrocyte progenitor cells.
An enriched or purified preparation of human mitotic oligodendrocyte progenitor cells, wherein the majority of cells in the enriched or purified preparation differentiate into O4 positive oligodendrocytes, when cultured in PDGF, FGF2, and NT3, and further develop into galactocerebroside positive oligodendrocytes in the presence of 5% FBS/IGF-1, the oligodendrocyte progenitor cells express A2B5 antigen and do not express O4 antigen.
An enriched or purified preparation of human mitotic oligodendrocyte progenitor cells, wherein the majority of cells in the enriched or purified preparation differentiate into O4 positive oligodendrocytes, when cultured in PDGF, FGF2, and NT3, and further develop into galactocerebroside positive oligodendrocytes in the presence of 5% FBS/IGF-1, the mitotic oligodendrocyte progenitor cells are from a fetal human and a human cyclic nucleotide phosphodiesterase gene P2 promoter is transcriptionally active in the oligodendrocyte progenitor cells.
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