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Molecular Mechanisms Underlying Ascl1-Mediated Astrocyte-to-Neuron Conversion

机译:依旧介导的星形胶质细胞对神经元转化的分子机制

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Direct neuronal reprogramming potentially provides valuable sources for cell-based therapies. Proneural gene Ascl1 converts astrocytes into induced neuronal (iN) cells efficiently both in?vitro and in?vivo . However, the underlying mechanisms are largely unknown. By combining RNA sequencing and chromatin immunoprecipitation followed by high-throughput sequencing, we found that the expression of 1,501 genes was markedly changed during the early stages of Ascl1 -induced astrocyte-to-neuron conversion and that the regulatory regions of 107 differentially expressed genes were directly bound by ASCL1. Among Ascl1 's direct targets, Klf10 regulates the neuritogenesis of iN cells at the early stage, Myt1 and Myt1l are critical for the electrophysiological maturation of iN cells, and Neurod4 and Chd7 are required for the efficient conversion of astrocytes into neurons. Together, this study provides more insights into understanding the molecular mechanisms underlying Ascl1 -mediated astrocyte-to-neuron conversion and will be of value for the application of direct neuronal reprogramming.
机译:直接神经元重编程可能为细胞疗法提供有价值的来源。脓性基因AsCl1在体外和体内有效地将星形胶质细胞转化为诱导的神经元(In)细胞。然而,潜在机制在很大程度上是未知的。通过组合RNA测序和染色质免疫沉淀,然后通过高通量测序,我们发现在ASCL1诱导的星形胶质细胞与神经元转化的早期阶段期间,1,501个基因的表达显着改变,并且107个差异表达基因的调节区域是直接受ASCL1绑定。在ASCL1的直接靶标中,KLF10调节在早期阶段的细胞中的神经发生,MyT1和MyT1L对于细胞的电生理学成熟至关重要,并且Neurod4和CHD7需要将星形胶质细胞的有效转化为神经元。这项研究在一起,了解更多洞察力,以了解ASCL1介导的星形胶质细胞与神经元转化率下面的分子机制,并将具有直接神经元重编程的价值。

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