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Induction of neural progenitor cells, oligodendrocyte progenitor cells, and oligodendrocytes by stem cell differentiation using landmark transcription factors

机译:使用标志性转录因子通过干细胞分化诱导神经祖细胞,少突胶质祖细胞和少突胶质细胞

摘要

A novel method for inducing human iPSC-derived neural progenitor cells, oligodendrocyte progenitor cells, and oligodendrocytes with unprecedented efficiency and functionality. The core of the present invention is a previously unknown mode at multiple key differentiation determinants along the pathway from pluripotency to ectoderm, neuroectoderm, from these to NPCs, from OPCs to oligodendrocytes. Is the use of transcription factors discovered experimentally. The present disclosure presents a specific combination and range of cell densities, reagents for the differentiation cascade of pluripotent stem cells into neural progenitor cells, oligodendrocyte progenitor cells, oligodendrocytes by a dynamically controlled cell growth process. Concerning induction and / or orientation utilizing concentrations, as well as specific combinations of mRNA.
机译:一种以前所未有的效率和功能诱导人iPSC衍生的神经祖细胞,少突胶质祖细胞和少突胶质细胞的新方法。本发明的核心是沿从多能性到外胚层,神经外胚层,从这些到NPC,从OPC到少突胶质细胞的途径的多个关键分化决定簇的先前未知的模式。是利用转录因子通过实验发现的。本公开提出了细胞密度,通过动态控制的细胞生长过程将多能干细胞分化级联成神经祖细胞,少突胶质祖细胞,少突胶质细胞的试剂的特定组合和范围。关于利用浓度以及mRNA的特定组合的诱导和/或定向。

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