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推动髓鞘形成——肌球蛋白表达的发育调控驱动少突胶质细胞形态分化。

Pushing myelination - developmental regulation of myosin expression drives oligodendrocyte morphological differentiation.

机构信息

International Iberian Nanotechnology Laboratory (INL), 4715-330 Braga, Portugal.

Instituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, 4200-135 Porto, Portugal.

出版信息

J Cell Sci. 2020 Aug 5;133(15):jcs232264. doi: 10.1242/jcs.232264.

Abstract

Oligodendrocytes are the central nervous system myelin-forming cells providing axonal electrical insulation and higher-order neuronal circuitry. The mechanical forces driving the differentiation of oligodendrocyte precursor cells into myelinating oligodendrocytes are largely unknown, but likely require the spatiotemporal regulation of the architecture and dynamics of the actin and actomyosin cytoskeletons. In this study, we analyzed the expression pattern of myosin motors during oligodendrocyte development. We report that oligodendrocyte differentiation is regulated by the synchronized expression and non-uniform distribution of several members of the myosin network, particularly non-muscle myosins 2B and 2C, which potentially operate as nanomechanical modulators of cell tension and myelin membrane expansion at different cell stages.This article has an associated First Person interview with the first author of the paper.

摘要

少突胶质细胞是中枢神经系统髓鞘形成细胞,为轴突提供电绝缘和更高阶的神经元回路。驱动少突胶质前体细胞分化为髓鞘形成少突胶质细胞的力学力在很大程度上是未知的,但可能需要肌动球蛋白细胞骨架的架构和动力学的时空调节。在这项研究中,我们分析了肌球蛋白马达在少突胶质细胞发育过程中的表达模式。我们报告说,少突胶质细胞分化受几种肌球蛋白网络成员的同步表达和不均匀分布调节,特别是非肌肉肌球蛋白 2B 和 2C,它们可能作为细胞张力和不同细胞阶段髓鞘膜扩张的纳米力学调节剂发挥作用。本文有与论文第一作者的相关第一人称访谈。

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本文引用的文献

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