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髓鞘轴突中分子域的组织和维持。

Organization and maintenance of molecular domains in myelinated axons.

机构信息

Curriculum in Neurobiology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.

出版信息

J Neurosci Res. 2013 May;91(5):603-22. doi: 10.1002/jnr.23197. Epub 2013 Feb 13.

Abstract

Over a century ago, Ramon y Cajal first proposed the idea of a directionality involved in nerve conduction and neuronal communication. Decades later, it was discovered that myelin, produced by glial cells, insulated axons with periodic breaks where nodes of Ranvier (nodes) form to allow for saltatory conduction. In the peripheral nervous system (PNS), Schwann cells are the glia that can either individually myelinate the axon from one neuron or ensheath axons of many neurons. In the central nervous system (CNS), oligodendrocytes are the glia that myelinate axons from different neurons. Review of more recent studies revealed that this myelination created polarized domains adjacent to the nodes. However, the molecular mechanisms responsible for the organization of axonal domains are only now beginning to be elucidated. The molecular domains in myelinated axons include the axon initial segment (AIS), where various ion channels are clustered and action potentials are initiated; the node, where sodium channels are clustered and action potentials are propagated; the paranode, where myelin loops contact with the axolemma; the juxtaparanode (JXP), where delayed-rectifier potassium channels are clustered; and the internode, where myelin is compactly wrapped. Each domain contains a unique subset of proteins critical for the domain's function. However, the roles of these proteins in axonal domain organization are not fully understood. In this review, we highlight recent advances on the molecular nature and functions of some of the components of each axonal domain and their roles in axonal domain organization and maintenance for proper neuronal communication.

摘要

一个多世纪以前,拉蒙·卡哈尔(Ramon y Cajal)首次提出了神经传导和神经元通讯中涉及方向性的观点。几十年后,人们发现,少突胶质细胞产生的髓鞘周期性地中断轴突,形成郎飞结(nodes),从而允许跳跃式传导。在周围神经系统(PNS)中,施万细胞(Schwann cells)可以单独对一个神经元的轴突进行髓鞘化,或者对许多神经元的轴突进行包裹。在中枢神经系统(CNS)中,少突胶质细胞对来自不同神经元的轴突进行髓鞘化。对最近的研究进行综述后发现,这种髓鞘化在郎飞结附近形成了极化的域。然而,负责轴突域组织的分子机制直到现在才开始被阐明。髓鞘化轴突中的分子域包括轴突起始段(axon initial segment,AIS),其中各种离子通道聚集,动作电位开始;郎飞结(node),其中钠通道聚集,动作电位传播;节间段(paranode),其中髓鞘环与轴膜接触; juxtaparanode(JXP),其中延迟整流钾通道聚集;和节间段(internode),其中髓鞘紧密包裹。每个域都包含一组独特的蛋白质,这些蛋白质对于域的功能至关重要。然而,这些蛋白质在轴突域组织中的作用还不完全清楚。在这篇综述中,我们重点介绍了每个轴突域的一些成分的分子性质和功能的最新进展,以及它们在轴突域组织和维持中的作用,以实现适当的神经元通讯。

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