首页> 外国专利> A PROCESS FOR DIFFERENTIATING A NEURAL PROGENITOR CELL TO A DOPAMINERGIC NEURAL CELL AND A CULTURE MEDIUM THEREFOR

A PROCESS FOR DIFFERENTIATING A NEURAL PROGENITOR CELL TO A DOPAMINERGIC NEURAL CELL AND A CULTURE MEDIUM THEREFOR

机译:将神经祖细胞分化为多巴胺能神经细胞的方法及其培养基

摘要

A process for differentiating a neural progenitor cell to a dopaminergic neural cell, and a culture medium therefor are provided to improve differentiation efficiency from a mesenchymal stem cell to the dopaminergic neural cell by using specific medium. The process for differentiating the neural progenitor cell to the dopaminergic neural cell comprises the steps of: (a) culturing the neural progenitor cell in N2 medium containing 20-100 ng/ml of fibroblast growth factor 8(FGF 8), 200-500 ng/ml of sonic hedgehog(SHH), 100-300 muM of ascorbic acid(AA) and 10-20 ng/ml of brain-derived neurotrophic factor(BDNF); and (b) culturing the cultured product in N2 medium containing 100-300 muM of ascorbic acid(AA), 10-20 ng/ml of brain-derived neurotrophic factor(BDNF), 2-20 ng/ml of glial cell-derived neurotrophic factor(GDNF) and 0.5-2 mM of dibutyryl cyclic adenosine monophosphate(dcAMP).
机译:提供了一种将神经祖细胞分化为多巴胺能神经细胞的方法及其培养基,以通过使用特定培养基来提高从间充质干细胞向多巴胺能神经细胞的分化效率。将神经祖细胞分化为多巴胺能神经细胞的过程包括以下步骤:(a)在含有20-100 ng / ml成纤维细胞生长因子8(FGF 8),200-500 ng的N2培养基中培养神经祖细胞/ ml的声音刺猬(SHH),100-300μM的抗坏血酸(AA)和10-20 ng / ml的脑源性神经营养因子(BDNF); (b)在含有100-300μM抗坏血酸(AA),10-20ng / ml脑源性神经营养因子(BDNF),2-20ng / ml神经胶质细胞源的N2培养基中培养培养产物。神经营养因子(GDNF)和0.5-2 mM的二丁酰基环磷酸腺苷(dcAMP)。

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