The Regulatory Roles of Cerebellar Glycosphingolipid Microdomains/Lipid Rafts

被引:6
|
作者
Komatsuya, Keisuke [1 ]
Kikuchi, Norihito [1 ]
Hirabayashi, Tetsuya [1 ]
Kasahara, Kohji [1 ]
机构
[1] Tokyo Metropolitan Inst Med Sci, Lab Biomembrane, Tokyo 1568506, Japan
关键词
lipid rafts; gangliosides; GPI-anchored proteins; Src-family kinases; heterotrimeric G proteins; CELL-ADHESION MOLECULE; ENRICHED MEMBRANE SUBDOMAINS; GPI-ANCHORED PROTEINS; LIPID RAFTS; PLASMA-MEMBRANE; KINASE LYN; RAT-BRAIN; RECEPTOR; GANGLIOSIDES; DOMAINS;
D O I
10.3390/ijms24065566
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid rafts are dynamic assemblies of glycosphingolipids, sphingomyelin, cholesterol, and specific proteins which are stabilized into platforms involved in the regulation of vital cellular processes. Cerebellar lipid rafts are cell surface ganglioside microdomains for the attachment of GPI-anchored neural adhesion molecules and downstream signaling molecules such as Src-family kinases and heterotrimeric G proteins. In this review, we summarize our recent findings on signaling in ganglioside GD3 rafts of cerebellar granule cells and several findings by other groups on the roles of lipid rafts in the cerebellum. TAG-1, of the contactin group of immunoglobulin superfamily cell adhesion molecules, is a phosphacan receptor. Phosphacan regulates the radial migration signaling of cerebellar granule cells, via Src-family kinase Lyn, by binding to TAG-1 on ganglioside GD3 rafts. Chemokine SDF-1 alpha, which induces the tangential migration of cerebellar granule cells, causes heterotrimeric G protein Go alpha translocation to GD3 rafts. Furthermore, the functional roles of cerebellar raft-binding proteins including cell adhesion molecule L1, heterotrimeric G protein Gs alpha, and L-type voltage-dependent calcium channels are discussed.
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页数:13
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