Max-Planck-Institute for Experimental Medicine, Hermann-Rein-Str. 3, Göttingen, Germany.
Curr Opin Cell Biol. 2013 Aug;25(4):512-9. doi: 10.1016/j.ceb.2013.04.007. Epub 2013 May 24.
The formation of myelin in the central nervous system is a multi-step process that involves coordinated cell-cell interactions and dramatic changes in plasma membrane architecture. First, oligodendrocytes send our numerous highly ramified processes to sample the axonal environment and decide which axon(s) to select for myelination. After this decision is made and individual axon to oligodendrocyte contact has been established, the exploratory process of the oligodendrocyte is converted into a flat sheath that spreads and winds along and around its associated axon to generate a multilayered membrane stack. By compaction of the opposing extracellular layers of membrane and extrusion of almost all cytoplasm from the intracellular domain of the sheath, the characteristic membrane-rich multi-lamellar structure of myelin is formed. Here we highlight recent advances in identifying biophysical and signalling based mechanisms that are involved in axonal selection and myelin sheath generation by oligodendrocytes. A thorough understanding of the mechanisms underlying these events is a prerequisite for the design of novel myelin repair strategies in demyelinating and dysmyelinating diseases.
中枢神经系统髓鞘的形成是一个多步骤的过程,涉及协调的细胞-细胞相互作用和质膜结构的巨大变化。首先,少突胶质细胞伸出它们众多高度分支的突起,以探测轴突环境,并决定对哪个(些)轴突进行髓鞘化。做出这个决定并建立了单个轴突与少突胶质细胞的接触后,少突胶质细胞的探索过程就会转化为一个扁平的鞘,它沿着并围绕着与之相关的轴突展开和缠绕,从而产生一个多层膜堆。通过膜的外胞质层的压缩和鞘内细胞质的几乎全部挤出,形成了具有特征性的富含膜的多层结构的髓鞘。在这里,我们重点介绍了最近在鉴定参与少突胶质细胞轴突选择和髓鞘鞘生成的基于生物物理和信号的机制方面的进展。深入了解这些事件的机制是设计脱髓鞘和发育不良疾病中髓鞘修复策略的前提。