Susuki Keiichiro, Rasband Matthew N, Tohyama Koujiro, Koibuchi Katsura, Okamoto Saori, Funakoshi Kei, Hirata Koichi, Baba Hiroko, Yuki Nobuhiro
Department of Neurology and Research Institute for Neuroimmunological Diseases, Dokkyo Medical University School of Medicine, Tochigi 321-0293, Japan.
J Neurosci. 2007 Apr 11;27(15):3956-67. doi: 10.1523/JNEUROSCI.4401-06.2007.
Voltage-gated Na+ (Na(v)) channels are highly concentrated at nodes of Ranvier in myelinated axons and facilitate rapid action potential conduction. Autoantibodies to gangliosides such as GM1 have been proposed to disrupt nodal Nav channels and lead to Guillain-Barré syndrome, an autoimmune neuropathy characterized by acute limb weakness. To test this hypothesis, we examined the molecular organization of nodes in a disease model caused by immunization with gangliosides. At the acute phase with progressing limb weakness, Na(v) channel clusters were disrupted or disappeared at abnormally lengthened nodes concomitant with deposition of IgG and complement products. Paranodal axoglial junctions, the nodal cytoskeleton, and Schwann cell microvilli, all of which stabilize Na(v) channel clusters, were also disrupted. The nodal molecules disappeared in lesions with complement deposition but no localization of macrophages. During recovery, complement deposition at nodes decreased, and Na(v) channels redistributed on both sides of affected nodes. These results suggest that Na(v) channel alterations occur as a consequence of complement-mediated disruption of interactions between axons and Schwann cells. Our findings support the idea that acute motor axonal neuropathy is a disease that specifically disrupts the nodes of Ranvier.
电压门控性钠(Na(v))通道高度集中于有髓轴突的郎飞结处,有助于动作电位的快速传导。有人提出,针对神经节苷脂(如GM1)的自身抗体会破坏结处的Nav通道,导致吉兰 - 巴雷综合征,这是一种以急性肢体无力为特征的自身免疫性神经病。为了验证这一假设,我们在由神经节苷脂免疫引起的疾病模型中研究了结的分子组织。在肢体无力进展的急性期,Na(v)通道簇在异常延长的结处被破坏或消失,同时伴有IgG和补体产物的沉积。郎飞结旁轴突 - 神经胶质连接、结处细胞骨架和施万细胞微绒毛,所有这些维持Na(v)通道簇稳定的结构也被破坏。结处分子在有补体沉积但无巨噬细胞定位的病变中消失。在恢复过程中,结处的补体沉积减少,Na(v)通道在受影响结的两侧重新分布。这些结果表明,Na(v)通道改变是补体介导的轴突与施万细胞之间相互作用破坏的结果。我们的研究结果支持急性运动轴索性神经病是一种特异性破坏郎飞结的疾病这一观点。