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少突胶质细胞分泌的连接蛋白多分子复合物在中枢神经系统结蛋白聚集中的作用。

Role of a Contactin multi-molecular complex secreted by oligodendrocytes in nodal protein clustering in the CNS.

机构信息

Sorbonne Université, Inserm, CNRS, UMR7225, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.

Assistance Publique-Hôpitaux de Paris, GH Pitié-Salpêtrière, Paris, France.

出版信息

Glia. 2019 Dec;67(12):2248-2263. doi: 10.1002/glia.23681. Epub 2019 Jul 22.

Abstract

The fast and reliable propagation of action potentials along myelinated fibers relies on the clustering of voltage-gated sodium channels at nodes of Ranvier. Axo-glial communication is required for assembly of nodal proteins in the central nervous system, yet the underlying mechanisms remain poorly understood. Oligodendrocytes are known to support node of Ranvier assembly through paranodal junction formation. In addition, the formation of early nodal protein clusters (or prenodes) along axons prior to myelination has been reported, and can be induced by oligodendrocyte conditioned medium (OCM). Our recent work on cultured hippocampal neurons showed that OCM-induced prenodes are associated with an increased conduction velocity (Freeman et al., 2015). We here unravel the nature of the oligodendroglial secreted factors. Mass spectrometry analysis of OCM identified several candidate proteins (i.e., Contactin-1, ChL1, NrCAM, Noelin2, RPTP/Phosphacan, and Tenascin-R). We show that Contactin-1 combined with RPTP/Phosphacan or Tenascin-R induces clusters of nodal proteins along hippocampal GABAergic axons. Furthermore, Contactin-1-immunodepleted OCM or OCM from Cntn1-null mice display significantly reduced clustering activity, that is restored by addition of soluble Contactin-1. Altogether, our results identify Contactin-1 secreted by oligodendrocytes as a novel factor that may influence early steps of nodal sodium channel cluster formation along specific axon populations.

摘要

动作电位沿有髓纤维的快速可靠传播依赖于电压门控钠离子通道在郎飞结处的聚集。轴突-神经胶质细胞通讯对于中枢神经系统中节点蛋白的组装是必需的,但潜在的机制仍知之甚少。少突胶质细胞通过形成连接蛋白复合体来支持郎飞结的组装。此外,据报道,在髓鞘形成之前,沿轴突形成早期节点蛋白簇(或前结),并且可以被少突胶质细胞条件培养基(OCM)诱导。我们最近在培养的海马神经元上的工作表明,OCM 诱导的前结与传导速度的增加有关(Freeman 等人,2015)。我们在这里揭示了少突胶质细胞分泌因子的性质。OCM 的质谱分析鉴定了几种候选蛋白(即,接触蛋白-1、ChL1、 NrCAM、Noelin2、RPTP/Phosphacan 和 Tenascin-R)。我们表明,接触蛋白-1与 RPTP/Phosphacan 或 Tenascin-R 结合可诱导海马 GABA 能轴突上节点蛋白的簇集。此外,Contactin-1 免疫耗尽的 OCM 或 Cntn1 敲除小鼠的 OCM 显示出明显降低的聚类活性,可通过添加可溶性 Contactin-1 来恢复。总之,我们的结果确定了少突胶质细胞分泌的 Contactin-1 是一种可能影响特定轴突群中节点钠通道簇形成早期步骤的新型因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2632/6851800/f7a7ee2b2f38/GLIA-67-2248-g001.jpg

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