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Ascl1 介导的星形胶质细胞向神经元转化的分子机制。

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

机构信息

Institute of Neuroscience, State Key Laboratory of Neuroscience, CAS center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai 200031, China; University of Chinese Academy of Sciences, Beijing 100049, China; Engineering Research Center of Molecular-imaging and Neuro-imaging of Ministry of Education, School of Life Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.

State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, 320 Yue Yang Road, Shanghai 200031, China.

出版信息

Stem Cell Reports. 2021 Mar 9;16(3):534-547. doi: 10.1016/j.stemcr.2021.01.006. Epub 2021 Feb 11.

Abstract

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.

摘要

直接神经元重编程为基于细胞的治疗提供了有价值的细胞来源。神经前体细胞基因 Ascl1 能够有效地将星形胶质细胞体外和体内转化为诱导性神经元 (iN) 细胞。然而,其潜在的机制在很大程度上仍是未知的。通过结合 RNA 测序和染色质免疫沉淀结合高通量测序,我们发现,在 Ascl1 诱导的星形胶质细胞向神经元转化的早期阶段,有 1501 个基因的表达明显改变,并且 107 个差异表达基因的调控区域被 ASCL1 直接结合。在 Ascl1 的直接靶点中,Klf10 调节 iN 细胞的早期神经突生成,Myt1 和 Myt1l 对 iN 细胞的电生理成熟至关重要,Neurod4 和 Chd7 则是将星形胶质细胞有效转化为神经元所必需的。总之,这项研究为理解 Ascl1 介导的星形胶质细胞向神经元转化的分子机制提供了更多的见解,并将有助于直接神经元重编程的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a53c/7940254/7a9d3acb75ec/fx1.jpg

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