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神经胶质βII spectrin 有助于连接蛋白形成和维持。

Glial βII Spectrin Contributes to Paranode Formation and Maintenance.

机构信息

Department of Neuroscience,

Department of Neuroscience, Cell Biology, and Physiology, Boonshoft School of Medicine, Wright State University, Dayton, Ohio 45435, and.

出版信息

J Neurosci. 2018 Jul 4;38(27):6063-6075. doi: 10.1523/JNEUROSCI.3647-17.2018. Epub 2018 May 31.

Abstract

Action potential conduction along myelinated axons depends on high densities of voltage-gated Na channels at the nodes of Ranvier. Flanking each node, paranodal junctions (paranodes) are formed between axons and Schwann cells in the peripheral nervous system (PNS) or oligodendrocytes in the CNS. Paranodal junctions contribute to both node assembly and maintenance. Despite their importance, the molecular mechanisms responsible for paranode assembly and maintenance remain poorly understood. βII spectrin is expressed in diverse cells and is an essential part of the submembranous cytoskeleton. Here, we show that Schwann cell βII spectrin is highly enriched at paranodes. To elucidate the roles of glial βII spectrin, we generated mutant mice lacking βII spectrin in myelinating glial cells by crossing mice with a floxed allele of with mice, and analyzed both male and female mice. Juvenile (4 weeks) and middle-aged (60 weeks) mutant mice showed reduced grip strength and sciatic nerve conduction slowing, whereas no phenotype was observed between 8 and 24 weeks of age. Consistent with these findings, immunofluorescence microscopy revealed disorganized paranodes in the PNS and CNS of both postnatal day 13 and middle-aged mutant mice, but not in young adult mutant mice. Electron microscopy confirmed partial loss of transverse bands at the paranodal axoglial junction in the middle-aged mutant mice in both the PNS and CNS. These findings demonstrate that a spectrin-based cytoskeleton in myelinating glia contributes to formation and maintenance of paranodal junctions. Myelinating glia form paranodal axoglial junctions that flank both sides of the nodes of Ranvier. These junctions contribute to node formation and maintenance and are essential for proper nervous system function. We found that a submembranous spectrin cytoskeleton is highly enriched at paranodes in Schwann cells. Ablation of βII spectrin in myelinating glial cells disrupted the paranodal cell adhesion complex in both peripheral and CNSs, resulting in muscle weakness and sciatic nerve conduction slowing in juvenile and middle-aged mice. Our data show that a spectrin-based submembranous cytoskeleton in myelinating glia plays important roles in paranode formation and maintenance.

摘要

动作电位沿有髓轴突的传导依赖于郎飞结处电压门控钠通道的高密度。在每个郎飞结的两侧,轴突和周围神经系统(PNS)中的施万细胞或中枢神经系统(CNS)中的少突胶质细胞之间形成了连接结(连接结)。连接结有助于节点的组装和维持。尽管它们很重要,但负责连接结组装和维持的分子机制仍知之甚少。βII spectrin 在多种细胞中表达,是亚膜细胞骨架的重要组成部分。在这里,我们表明施万细胞βII spectrin 在连接结处高度富集。为了阐明神经胶质βII spectrin 的作用,我们通过将带有 floxed 等位基因的小鼠与 小鼠杂交,在有髓鞘形成的神经胶质细胞中生成了缺乏βII spectrin 的突变小鼠,并分析了雄性和雌性小鼠。幼鼠(4 周龄)和中年(60 周龄)突变小鼠表现出握力下降和坐骨神经传导速度减慢,而在 8 至 24 周龄之间没有观察到表型。与这些发现一致,免疫荧光显微镜显示,出生后第 13 天和中年突变小鼠的 PNS 和 CNS 中的连接结排列紊乱,但年轻成年突变小鼠没有。电子显微镜证实,中年突变小鼠的 PNS 和 CNS 中,连接结的轴突-神经胶质交界处的横向带部分缺失。这些发现表明,髓鞘形成神经胶质中的 spectrin 基细胞骨架有助于连接结的形成和维持。髓鞘形成的神经胶质形成连接结,两侧为郎飞结。这些连接结有助于节点的形成和维持,是神经系统正常功能所必需的。我们发现,施万细胞中的连接结处高度富集亚膜 spectrin 细胞骨架。髓鞘形成神经胶质细胞中βII spectrin 的缺失破坏了周围和中枢神经系统中的连接结细胞粘附复合物,导致幼年和中年小鼠出现肌肉无力和坐骨神经传导速度减慢。我们的数据表明,髓鞘形成神经胶质中的 spectrin 基亚膜细胞骨架在连接结的形成和维持中发挥重要作用。

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