Nie Du-Yu, Ma Quan-Hong, Law Janice W S, Chia Chern-Pang, Dhingra Narender K, Shimoda Yasushi, Yang Wu-Lin, Gong Neng, Chen Qing-Wen, Xu Gang, Hu Qi-Dong, Chow Pierce K H, Ng Yee-Kong, Ling Eng-Ang, Watanabe Kazutada, Xu Tian-Le, Habib Amyn A, Schachner Melitta, Xiao Zhi-Cheng
Institute of Molecular and Cell Biology, Singapore.
Neuron Glia Biol. 2006 Aug;2(3):151-64. doi: 10.1017/S1740925X06000251.
The molecular mechanisms underlying the involvement of oligodendrocytes in formation of the nodes of Ranvier (NORs) remain poorly understood. Here we show that oligodendrocyte-myelin glycoprotein (OMgp) aggregates specifically at NORs. Nodal location of OMgp does not occur along demyelinated axons of either Shiverer or proteolipid protein (PLP) transgenic mice. Over-expression of OMgp in OLN-93 cells facilitates process outgrowth. In transgenic mice in which expression of OMgp is down-regulated, myelin thickness declines, and lateral oligodendrocyte loops at the node-paranode junction are less compacted and even join together with the opposite loops, which leads to shortened nodal gaps. Notably, each of these structural abnormalities plus modest down-regulation of expression of Na(+) channel alpha subunit result in reduced conduction velocity in the spinal cords of the mutant mice. Thus, OMgp that is derived from glia has distinct roles in regulating nodal formation and function during CNS myelination.
少突胶质细胞参与郎飞结(NORs)形成的分子机制仍知之甚少。在此我们表明,少突胶质细胞髓鞘糖蛋白(OMgp)特异性聚集在NORs处。OMgp的结区定位不会出现在颤抖小鼠或蛋白脂蛋白(PLP)转基因小鼠的脱髓鞘轴突上。在OLN - 93细胞中过表达OMgp可促进突起生长。在OMgp表达下调的转基因小鼠中,髓鞘厚度减小,结旁结交界处的外侧少突胶质细胞环不那么紧密,甚至与相对的环连接在一起,这导致结间隙缩短。值得注意的是,这些结构异常中的每一种加上Na(+)通道α亚基表达的适度下调都会导致突变小鼠脊髓中的传导速度降低。因此,来源于神经胶质细胞的OMgp在中枢神经系统髓鞘形成过程中对调节结的形成和功能具有独特作用。