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

机译:MicroRNA miR-204调节植物中少压细胞的增殖和分化

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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.
机译:少突胶质用髓鞘包裹和物理屏蔽中枢神经系统的轴突,导致信号转导和准确的神经元功能。从不成熟的少突胶质细胞前体细胞(OPC)到髓鞘寡核细胞(OLS)的复合寡突发性发育深切依赖于SOX蛋白家族的转录因子的活性。最近关键调节剂SOX10的靶基因已扩展到MicroRNA。在这里,我们将MIR-204报告为SOX10的新转录目标。 miR-204的调节区域显示出报告基因测定和电磁体移测的SOX10的反应性和结合。一旦表达,MIR-204抑制OPC增殖,并在SOX10存在下,从原发性大鼠和小鼠寡突培养物中的过表达明显,促进在OL中的分化。表型至少部分地由促进的Pro-proMiferative CCND2和分化抑制SOX4依赖性抑制引起的。这些发现认为转录活化剂SOX10迫使少突术细胞从细胞周期出来并通过MiR-204诱导开始分化。

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