Thaxton Courtney, Bhat Manzoor A
Department of Cell and Molecular Physiology, Curriculum in Neurobiology, UNC-Neuroscience Center and Neurodevelopmental Disorders Research Center, University of North Carolina School of Medicine, Chapel Hill, NC 27599-7545, USA.
Results Probl Cell Differ. 2009;48:1-28. doi: 10.1007/400_2009_3.
During evolution, as organisms increased in complexity and function, the need for the ensheathment and insulation of axons by glia became vital for faster conductance of action potentials in nerves. Myelination, as the process is termed, facilitates the formation of discrete domains within the axolemma that are enriched in ion channels, and macromolecular complexes consisting of cell adhesion molecules and cytoskeletal regulators. While it is known that glia play a substantial role in the coordination and organization of these domains, the mechanisms involved and signals transduced between the axon and glia, as well as the proteins regulating axo-glial junction formation remain elusive. Emerging evidence has shed light on the processes regulating myelination and domain differentiation, and key molecules have been identified that are required for their assembly and maintenance. This review highlights these recent findings, and relates their significance to domain disorganization as seen in several demyelinating disorders and other neuropathies.
在进化过程中,随着生物体的复杂性和功能不断增加,神经胶质细胞对轴突进行包裹和绝缘对于神经中动作电位的更快传导变得至关重要。这个过程被称为髓鞘形成,它促进了轴膜内富含离子通道以及由细胞粘附分子和细胞骨架调节因子组成的大分子复合物的离散结构域的形成。虽然已知神经胶质细胞在这些结构域的协调和组织中发挥着重要作用,但轴突与神经胶质细胞之间涉及的机制、转导的信号以及调节轴突-胶质细胞连接形成的蛋白质仍然不清楚。新出现的证据揭示了调节髓鞘形成和结构域分化的过程,并且已经鉴定出了它们组装和维持所需的关键分子。这篇综述强调了这些最新发现,并将它们的重要性与几种脱髓鞘疾病和其他神经病变中出现的结构域紊乱联系起来。