敲除非常规肌球蛋白ID的表达可诱导少突胶质细胞的形态变化

IF 3.9 4区 医学 Q2 NEUROSCIENCES
ASN NEURO Pub Date : 2016-09-21 Print Date: 2016-10-01 DOI:10.1177/1759091416669609
Reiji Yamazaki, Tomoko Ishibashi, Hiroko Baba, Yoshihide Yamaguchi
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引用次数: 0

摘要

髓鞘是一种特殊的多纤层结构,参与神经系统的各种功能。在中枢神经系统中,少突胶质细胞(OL)产生髓鞘,并具有独特的形态。少突胶质细胞具有与细胞骨架组织相关的动态膜分选系统,有助于髓鞘的生成。最近有报道称,肌动蛋白丝的组装和拆卸对髓鞘化至关重要。然而,在髓鞘化过程中与肌动蛋白丝结合的伙伴肌球蛋白分子尚未确定。一个候选肌球蛋白是非常规肌球蛋白 ID(Myo1d),它分布于整个中枢神经系统髓鞘中,但其功能仍不清楚。我们在此报告,Myo1d 与髓鞘蛋白脂质(PLP)一起在 OL 分化的后期阶段表达。此外,Myo1d分布在培养的OL髓鞘样膜的前缘,主要与肌动蛋白丝、2',3'-环核苷酸磷酸二酯酶共聚焦,部分与PLP共聚焦。用特异性 siRNA 敲除 Myo1d 可诱导明显的形态学变化,如突触回缩和髓鞘样膜变性,最终导致细胞凋亡。此外,通过 siRNA 缺失 Myo1d 会导致细胞内 PLP 转运受损。这些结果表明,在髓鞘的形成和维持过程中,Myo1d可能在包裹或转运髓鞘膜蛋白方面对膜的动力学做出了贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Knockdown of Unconventional Myosin ID Expression Induced Morphological Change in Oligodendrocytes.

Myelin is a special multilamellar structure involved in various functions in the nervous system. In the central nervous system, the oligodendrocyte (OL) produces myelin and has a unique morphology. OLs have a dynamic membrane sorting system associated with cytoskeletal organization, which aids in the production of myelin. Recently, it was reported that the assembly and disassembly of actin filaments is crucial for myelination. However, the partner myosin molecule which associates with actin filaments during the myelination process has not yet been identified. One candidate myosin is unconventional myosin ID (Myo1d) which is distributed throughout central nervous system myelin; however, its function is still unclear. We report here that Myo1d is expressed during later stages of OL differentiation, together with myelin proteolipid protein (PLP). In addition, Myo1d is distributed at the leading edge of the myelin-like membrane in cultured OL, colocalizing mainly with actin filaments, 2',3'-cyclic nucleotide phosphodiesterase and partially with PLP. Myo1d-knockdown with specific siRNA induces significant morphological changes such as the retraction of processes and degeneration of myelin-like membrane, and finally apoptosis. Furthermore, loss of Myo1d by siRNA results in the impairment of intracellular PLP transport. Together, these results suggest that Myo1d may contribute to membrane dynamics either in wrapping or transporting of myelin membrane proteins during formation and maintenance of myelin.

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来源期刊
ASN NEURO
ASN NEURO NEUROSCIENCES-
CiteScore
7.70
自引率
4.30%
发文量
35
审稿时长
>12 weeks
期刊介绍: ASN NEURO is an open access, peer-reviewed journal uniquely positioned to provide investigators with the most recent advances across the breadth of the cellular and molecular neurosciences. The official journal of the American Society for Neurochemistry, ASN NEURO is dedicated to the promotion, support, and facilitation of communication among cellular and molecular neuroscientists of all specializations.
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