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

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

机译:将神经祖细胞分化为胆碱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 cholinergic neural cell, and a culture medium therefor are provided to differentiate adult stem cells containing mesenchymal stem cell derived from cord blood into the cholinergic neural cell in vitro, and improve differentiation rate from the neural progenitor cell to the cholinergic neural cell. The process for differentiating the neural progenitor cell into the cholinergic neural cell comprises the steps of: (a) culturing the neural progenitor cell in N2 medium containing 50-500 ng/ml of sonic hedgehog(SHH) and 0.1-2 muM of retinoic acid(RA); (b) culturing the culture product of step(a) in N2 medium containing 1-20 ng/ml of basic fibroblast growth factor(bFGF) and 50-500 ng/ml of sonic hedgehog(SHH); and (c) culturing the culture product of step(b) in N2 medium containing 100-300 muM of ascorbic acid(AA) and 10-20 ng/ml of brain-derived neurotrophic factor(BDNF), wherein the neural progenitor cell is obtained from the mesenchymal stem cell derived from cord blood.
机译:提供了一种将神经祖细胞分化为胆碱能神经细胞的方法及其培养基,以在体外将含有源自脐带血的间充质干细胞的成体干细胞分化为胆碱能神经细胞,并提高了从神经祖细胞的分化率。细胞到胆碱能神经细胞。将神经祖细胞分化为胆碱能神经细胞的过程包括以下步骤:(a)在含有50-500 ng / ml的声波刺猬(SHH)和0.1-2μM视黄酸的N2培养基中培养神经祖细胞。 (RA); (b)在含有1-20ng / ml的碱性成纤维细胞生长因子(bFGF)和50-500ng / ml的声波刺猬(SHH)的N2培养基中培养步骤(a)的培养产物; (c)在含有100-300μM抗坏血酸(AA)和10-20ng / ml脑源性神经营养因子(BDNF)的N2培养基中培养步骤(b)的培养产物,其中神经祖细胞是来源于脐带血的间充质干细胞。

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