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少突胶质细胞连接蛋白 47 和星形胶质细胞连接蛋白 43 缝隙连接的定向偶联。

Directional coupling of oligodendrocyte connexin-47 and astrocyte connexin-43 gap junctions.

机构信息

Unit of Experimental Neurology and Neurobiology, "Ramón y Cajal" Hospital-IRYCIS, Carretera de Colmenar km 9, Madrid, 28034, Spain.

Structural Biology Unit of CIC bioGUNE, Bizkaia Technology Park, Building 800, Derio, 48160, Spain.

出版信息

Glia. 2018 Nov;66(11):2340-2352. doi: 10.1002/glia.23471. Epub 2018 Aug 25.

DOI:10.1002/glia.23471
PMID:30144323
Abstract

Intercellular communication via gap junction channels between oligodendrocytes and between astrocytes as well as between these cell types is essential to maintain the integrity of myelin in the central nervous system. Oligodendrocyte gap junction connexin-47 (Cx47) is a key element in this crosstalk and indeed, mutations in human Cx47 cause severe myelin disorders. However, the permeation properties of channels of Cx47 alone and in heterotypic combination with astrocyte Cx43 remain unclear. We show here that Cx47 contains three extra residues at 5' amino-terminus that play a critical role in the channel pore structure and account for relative low ionic conductivity, cationic permselectivity and voltage-gating properties of oligodendrocyte-oligodendrocyte Cx47 channels. Regarding oligodendrocyte-astrocyte coupling, heterotypic channels formed by Cx47 with Cx43 exhibit ionic and chemical rectification, which creates a directional diffusion barrier for the movement of ions and larger negatively charged molecules from cells expressing Cx47 to those with Cx43. The restrictive permeability of Cx47 channels and the diffusion barrier of Cx47-Cx43 channels was abolished by a mutation associated with leukodystrophy, the Cx47P90S, suggesting a novel pathogenic mechanism underlying myelin disorders that involves alterations in the panglial permeation.

摘要

细胞间通讯通过少突胶质细胞和星形胶质细胞之间以及这些细胞类型之间的缝隙连接通道对于维持中枢神经系统髓鞘的完整性至关重要。少突胶质细胞缝隙连接连接蛋白-47(Cx47)是这种串扰的关键要素,事实上,人类 Cx47 的突变会导致严重的髓鞘疾病。然而,Cx47 单独和与星形胶质细胞 Cx43 异质组合的通道的渗透特性仍不清楚。我们在这里表明,Cx47 在 5'氨基末端有三个额外的残基,这些残基在通道孔结构中起着关键作用,并解释了少突胶质细胞-少突胶质细胞 Cx47 通道相对较低的离子电导率、阳离子选择性和电压门控特性的原因。关于少突胶质细胞-星形胶质细胞偶联,Cx47 与 Cx43 形成的异型通道表现出离子和化学整流,这为从表达 Cx47 的细胞向表达 Cx43 的细胞中离子和较大带负电荷的分子的运动创建了一个定向扩散屏障。与白质营养不良相关的突变(Cx47P90S)消除了 Cx47 通道的限制渗透性和 Cx47-Cx43 通道的扩散屏障,这表明涉及潘盖尔渗透改变的髓鞘疾病的新发病机制。

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