共 41 条
Transmembrane scaffolding proteins in the formation and stability of nodes of Ranvier
被引:19
作者:

Girault, JA
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机构: INSERM, Signal Transduct & Plast Nervous Syst, F-75005 Paris, France

Oguievetskaia, K
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机构: INSERM, Signal Transduct & Plast Nervous Syst, F-75005 Paris, France

Carnaud, M
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h-index: 0
机构: INSERM, Signal Transduct & Plast Nervous Syst, F-75005 Paris, France

Denisenko-Nehrbass, N
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机构: INSERM, Signal Transduct & Plast Nervous Syst, F-75005 Paris, France

Goutebroze, L
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h-index: 0
机构: INSERM, Signal Transduct & Plast Nervous Syst, F-75005 Paris, France
机构:
[1] INSERM, Signal Transduct & Plast Nervous Syst, F-75005 Paris, France
[2] Univ Paris 06, INSERM, U536, Inst Fer Moulin, F-75005 Paris, France
关键词:
D O I:
10.1016/S0248-4900(03)00073-X
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 [细胞生物学];
090102 [作物遗传育种];
摘要:
The function of myelinated fibers depends on the clustering of sodium channels at nodes of Ranvier, the integrity of the myelin sheath, and the existence of tight axoglial junctions at paranodes, on either sides of the nodes. While the ultrastructure of these regions has been known for several decades, recent progress has been accomplished in the identification of proteins essential for their organization, which depends on the interplay between axons and myelinating glial cells. Evolutionary conserved intercellular multimolecular complexes comprising proteins of the Neurexin IV/Caspr/paranodin (NCP) family and of the immunoglobulin-like cell adhesion molecules superfamily, are essential components for the axoglial contacts at the level of paranodes and juxtaparanodes. These complexes are able to interact with cytoplasmic proteins of the band 4.1 family, providing possible links to the axonal cytoskeleton. While the identification of these proteins represents a significant progress for understanding axoglial contacts, they also raise exciting questions concerning the molecular organization of these contacts and the mechanisms of their local enrichment. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
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页码:447 / 452
页数:6
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