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Small Molecules Efficiently Reprogram Human Astroglial Cells into Functional Neurons

机译:小分子将人类星形胶质细胞有效地重编程为功能性神经元

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摘要

We have recently demonstrated that reactive glial cells can be directly reprogrammed into functional neurons by a single neural transcription factor, NeuroD1. Here we report that a combination of small molecules can also reprogram human astrocytes in culture into fully functional neurons. We demonstrate that sequential exposure of human astrocytes to a cocktail of nine small molecules that inhibit glial but activate neuronal signaling pathways can successfully reprogram astrocytes into neurons in 8-10 days. This chemical reprogramming is mediated through epigenetic regulation and involves transcriptional activation of NEUROD1 and NEUROGENIN2. The human astrocyte-converted neurons can survive for >5 months in culture and form functional synaptic networks with synchronous burst activities. The chemically reprogrammed human neurons can also survive for >1 month in the mouse brain in vivo and integrate into local circuits. Our study opens a new avenue using chemical compounds to reprogram reactive glial cells into functional neurons.
机译:我们最近证明,反应性神经胶质细胞可以通过单个神经转录因子NeuroD1直接重编程为功能性神经元。在这里,我们报道小分子的组合也可以将人类星形胶质细胞在培养过程中重新编程为功能齐全的神经元。我们证明了人类星形胶质细胞对九种抑制神经胶质但激活神经元信号通路的小分子混合物的连续暴露可以在8-10天之内成功地将星形胶质细胞重新编程为神经元。这种化学重编程通过表观遗传调控介导,涉及NEUROD1和NEUROGENIN2的转录激活。人类星形胶质细胞转化的神经元可以在培养中存活> 5个月,并形成具有同步爆发活动的功能性突触网络。化学重编程的人类神经元在小鼠体内还可以存活超过1个月,并整合到局部回路中。我们的研究为使用化学化合物将神经胶质细胞重编程为功能性神经元开辟了一条新途径。

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