| Literature DB >> 17428969 |
Keiichiro Susuki1, Matthew N Rasband, Koujiro Tohyama, Katsura Koibuchi, Saori Okamoto, Kei Funakoshi, Koichi Hirata, Hiroko Baba, Nobuhiro Yuki.
Abstract
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.Entities:
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Year: 2007 PMID: 17428969 PMCID: PMC6672537 DOI: 10.1523/JNEUROSCI.4401-06.2007
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167