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The Regulatory Roles of Cerebellar Glycosphingolipid Microdomains/Lipid Rafts.
Komatsuya, Keisuke; Kikuchi, Norihito; Hirabayashi, Tetsuya; Kasahara, Kohji.
Affiliation
  • Komatsuya K; Laboratory of Biomembrane, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.
  • Kikuchi N; Laboratory of Biomembrane, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.
  • Hirabayashi T; Laboratory of Biomembrane, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.
  • Kasahara K; Laboratory of Biomembrane, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.
Int J Mol Sci ; 24(6)2023 Mar 14.
Article in En | MEDLINE | ID: mdl-36982638
ABSTRACT
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-1α, which induces the tangential migration of cerebellar granule cells, causes heterotrimeric G protein Goα translocation to GD3 rafts. Furthermore, the functional roles of cerebellar raft-binding proteins including cell adhesion molecule L1, heterotrimeric G protein Gsα, and L-type voltage-dependent calcium channels are discussed.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycosphingolipids / Receptor-Like Protein Tyrosine Phosphatases, Class 5 Language: En Journal: Int J Mol Sci Year: 2023 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycosphingolipids / Receptor-Like Protein Tyrosine Phosphatases, Class 5 Language: En Journal: Int J Mol Sci Year: 2023 Document type: Article Affiliation country: Japón