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微小RNA miR-204调控培养的少突胶质细胞的增殖与分化。

MicroRNA miR-204 regulates proliferation and differentiation of oligodendroglia in culture.

作者信息

Wittstatt Jan, Weider Matthias, Wegner Michael, Reiprich Simone

机构信息

Institut für Biochemie, Emil-Fischer-Zentrum, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

出版信息

Glia. 2020 Oct;68(10):2015-2027. doi: 10.1002/glia.23821. Epub 2020 Mar 16.

Abstract

Oligodendrocytes wrap and physically shield axons of the central nervous system with myelin sheaths, resulting in rapid signal transduction and accurate neuronal function. The complex oligodendroglial development from immature oligodendrocyte precursor cells (OPCs) to myelinating oligodendrocytes (OLs) is profoundly dependent on the activity of transcription factors of the Sox protein family. Target genes of the crucial regulator Sox10 have recently been expanded to microRNAs. Here, we report miR-204 as a novel transcriptional target of Sox10. Regulatory regions of miR-204 show responsiveness to and binding of Sox10 in reporter gene assays and electromobility shift assays. Once expressed, miR-204 inhibits OPC proliferation and facilitates differentiation into OLs in the presence of Sox10 as evident from overexpression in primary rat and mouse oligodendroglial cultures. Phenotypes are at least in part caused by miR-204-dependent repression of the pro-proliferative Ccnd2 and the differentiation inhibiting Sox4. These findings argue that the transcriptional activator Sox10 forces oligodendroglial cells to exit the cell cycle and start differentiation by gene inhibition via miR-204 induction.

摘要

少突胶质细胞用髓鞘包裹并物理性地保护中枢神经系统的轴突,从而实现快速的信号转导和精确的神经元功能。从少突胶质前体细胞(OPC)到髓鞘形成少突胶质细胞(OL)的复杂少突胶质细胞发育过程,在很大程度上依赖于Sox蛋白家族转录因子的活性。关键调节因子Sox10的靶基因最近已扩展到微小RNA。在此,我们报告miR-204是Sox10的一个新的转录靶标。在报告基因分析和电泳迁移率变动分析中,miR-204的调控区域显示出对Sox10的反应性和结合性。一旦表达,miR-204在原代大鼠和小鼠少突胶质细胞培养中过表达时,会抑制OPC增殖并促进其向OL分化。这些表型至少部分是由miR-204对促增殖的Ccnd2和抑制分化的Sox4的依赖性抑制引起的。这些发现表明,转录激活因子Sox10通过诱导miR-204抑制基因,促使少突胶质细胞退出细胞周期并开始分化。

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