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Direct reprogramming of human astrocytes into neural stem cells and neurons

机译:将人类星形胶质细胞直接重编程为神经干细胞和神经元

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Generating neural stem cells and neurons from reprogrammed human astrocytes is a potential strategy for neurological repair. Here we show dedifferentiation of human cortical astrocytes into the neural stem/progenitor phenotype to obtain progenitor and mature cells with a neural fate. Ectopic expression of the reprogramming factors OCT4, SOX2, or NANOG into astrocytes in specific cytokine/culture conditions activated the neural stem gene program and induced generation of cells expressing neural stem/precursor markers. Pure CD44 + mature astrocytes also exhibited this lineage commitment change and did not require passing through a pluripotent state. These astrocyte-derived neural stem cells gave rise to neurons, astrocytes, and oligodendrocytes and showed in vivo engraftment properties. ASCL1 expression further promoted neuronal phenotype acquisition in vitro and in vivo. Methylation analysis showed that epigenetic modifications underlie this process. The restoration of multipotency from human astrocytes has potential in cellular reprogramming of endogenous central nervous system cells in neurological disorders.
机译:从重编程的人类星形胶质细胞生成神经干细胞和神经元是神经修复的潜在策略。在这里,我们显示人类皮层星形胶质细胞去分化为神经干/祖细胞表型,以获得具有神经命运的祖细胞和成熟细胞。在特定的细胞因子/培养条件下,重编程因子OCT4,SOX2或NANOG在星形胶质细胞中的异位表达激活了神经干基因程序,并诱导了表达神经干/前体标志物的细胞的生成。纯CD44 +成熟的星形胶质细胞也表现出这种谱系承诺变化,并且不需要通过多能状态。这些源自星形胶质细胞的神经干细胞产生神经元,星形胶质细胞和少突胶质细胞,并显示出体内植入特性。 ASCL1表达进一步促进了体外和体内神经元表型的获得。甲基化分析表明,表观遗传修饰是该过程的基础。从人类星形胶质细胞恢复多能性在神经系统疾病中内源性中枢神经系统细胞的细胞重编程中具有潜力。

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