Aix-Marseille Université, CNRS, CRN2M-UMR7286 Marseille, France.
Front Cell Neurosci. 2013 Oct 29;7:196. doi: 10.3389/fncel.2013.00196.
Specific cell adhesion molecules (CAMs) are dedicated to the formation of axo-glial contacts at the nodes of Ranvier of myelinated axons. They play a central role in the organization and maintenance of the axonal domains: the node, paranode, and juxtaparanode. In particular, CAMs are essential for the accumulation of voltage-gated sodium channels at the nodal gap that ensures the rapid and saltatory propagation of the action potentials (APs). The mechanisms regulating node formation are distinct in the central and peripheral nervous systems, and recent studies have highlighted the relative contribution of paranodal junctions and nodal extracellular matrix. In addition, CAMs at the juxtaparanodal domains mediate the clustering of voltage-gated potassium channels which regulate the axonal excitability. In several human pathologies, the axo-glial contacts are altered leading to disruption of the nodes of Ranvier or mis-localization of the ion channels along the axons. Node alterations and the failure of APs to propagate correctly from nodes to nodes along the axons both contribute to the disabilities in demyelinating diseases. This article reviews the mechanisms regulating the association of the axo-glial complexes and the role of CAMs in inherited and acquired neurological diseases.
特定的细胞粘附分子(CAM)专门用于形成有髓轴突的郎飞结处的轴突-胶质接触。它们在轴突结构域的组织和维持中起着核心作用:节点、旁节点和近旁节点。特别是,CAM 对于在节点间隙处积聚电压门控钠离子通道是必不可少的,这确保了动作电位(AP)的快速跳跃传播。调节节点形成的机制在中枢和周围神经系统中是不同的,最近的研究强调了旁节点连接和节点细胞外基质的相对贡献。此外,近旁节点域的 CAM 介导电压门控钾通道的簇集,调节轴突兴奋性。在几种人类病理学中,轴突-胶质接触发生改变,导致郎飞结的破坏或离子通道沿着轴突的错误定位。节点改变以及 AP 不能正确地从节点传播到轴突上的节点,都导致脱髓鞘疾病的残疾。本文综述了调节轴突-胶质复合物的关联的机制以及 CAM 在遗传性和获得性神经疾病中的作用。