Pedraza L, Huang J K, Colman D R
The Corinne Goldsmith Dickinson Center for Multiple Sclerosis, Department of Neurology, The Mount Sinai School of Medicine, 1425 Madison Avenue, New York, NY 10029, USA.
Neuron. 2001 May;30(2):335-44. doi: 10.1016/s0896-6273(01)00306-3.
On axonal surfaces that flank the node of Ranvier and in overlying glial paranodal loops, proteins are arranged within circumscribed microdomains that defy explanation by conventional biosynthetic mechanisms. We postulate that the constraint of proteins to these loci is accomplished in part by discriminative membrane-embedded molecular sieves and diffusion barriers, which serve to organize and redistribute proteins after delivery by vesicular transport to neural cell plasma membranes. One sieve likely comprises a moveable, macromolecular scaffold of axonal and glial cell-derived transmembrane adhesion molecules and their associated cytoplasmic binding partners, located at the ends of each elongating myelin internode; this sieve contributes to restricting the sodium channel complexes to the node. We also anticipate the existence of a passive paranodal diffusion barrier at the myelin/noncompact membrane border, which prohibits protein diffusion out of contiguous paranodal membranes.
在郎飞结两侧的轴突表面以及覆盖其上的胶质旁结环中,蛋白质排列在特定的微结构域内,这无法用传统的生物合成机制来解释。我们推测,蛋白质在这些位点的受限部分是由具有鉴别性的膜嵌入分子筛和扩散屏障完成的,这些分子筛和扩散屏障在通过囊泡运输将蛋白质递送至神经细胞质膜后,起到组织和重新分布蛋白质的作用。一种分子筛可能由轴突和胶质细胞衍生的跨膜粘附分子及其相关的细胞质结合伴侣组成的可移动大分子支架构成,位于每个延长的髓鞘节间的末端;这种分子筛有助于将钠通道复合物限制在结处。我们还预期在髓鞘/非致密膜边界存在一个被动的旁结扩散屏障,它可阻止蛋白质从相邻的旁结膜中扩散出去。