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N-WASp 对于施万细胞细胞骨架动态、正常髓鞘基因表达和周围神经髓鞘形成是必需的。

N-WASp is required for Schwann cell cytoskeletal dynamics, normal myelin gene expression and peripheral nerve myelination.

机构信息

Department of Haematology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.

出版信息

Development. 2011 Apr;138(7):1329-37. doi: 10.1242/dev.058677.

Abstract

Schwann cells elaborate myelin sheaths around axons by spirally wrapping and compacting their plasma membranes. Although actin remodeling plays a crucial role in this process, the effectors that modulate the Schwann cell cytoskeleton are poorly defined. Here, we show that the actin cytoskeletal regulator, neural Wiskott-Aldrich syndrome protein (N-WASp), is upregulated in myelinating Schwann cells coincident with myelin elaboration. When N-WASp is conditionally deleted in Schwann cells at the onset of myelination, the cells continue to ensheath axons but fail to extend processes circumferentially to elaborate myelin. Myelin-related gene expression is also severely reduced in the N-WASp-deficient cells and in vitro process and lamellipodia formation are disrupted. Although affected mice demonstrate obvious motor deficits these do not appear to progress, the mutant animals achieving normal body weights and living to advanced age. Our observations demonstrate that N-WASp plays an essential role in Schwann cell maturation and myelin formation.

摘要

许旺细胞通过螺旋包裹和压缩其质膜来围绕轴突形成髓鞘。尽管肌动蛋白重塑在这个过程中起着关键作用,但调节许旺细胞细胞骨架的效应物还未被明确界定。在这里,我们发现肌动蛋白细胞骨架调节剂神经 Wiskott-Aldrich 综合征蛋白(N-WASp)在髓鞘形成时在髓鞘形成的许旺细胞中上调。当 N-WASp 在髓鞘形成开始时在许旺细胞中条件性缺失时,细胞继续包裹轴突,但未能围绕轴突延伸以形成髓鞘。在 N-WASp 缺陷细胞中和体外过程中,髓鞘相关基因的表达也严重减少,并且过程和片状伪足的形成受到破坏。尽管受影响的小鼠表现出明显的运动缺陷,但这些缺陷似乎没有进展,突变动物达到了正常体重并活到老年。我们的观察表明,N-WASp 在许旺细胞成熟和髓鞘形成中发挥着重要作用。

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