The sphingosine 1-phosphate receptor 5 and sphingosine kinases 1 and 2 are localised in centrosomes: Possible role in regulating cell division

被引:29
|
作者
Gillies, Laura [2 ]
Lee, Sue Chin [2 ]
Long, Jaclyn S. [2 ]
Ktistakis, Nicholas [2 ]
Pyne, Nigel J. [1 ]
Pyne, Susan [2 ]
机构
[1] Babraham Inst, Dept Signaling, Cambridge CB2 4AT, England
[2] Univ Strathclyde, Cell Biol Grp, SIPBS, Glasgow G4 0NR, Lanark, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
Sphingosine; 1-phosphate; Centrosomal; Mitosis; Sphingosine kinase; Sphingosine 1-phosphate receptor 5; G-ALPHA; PLASMA-MEMBRANE; GOLOCO MOTIF; PROTEIN; INTEGRATION; METABOLISM; ACTIVATION; INHIBITORS; TYPE-2; GAMMA;
D O I
10.1016/j.cellsig.2009.01.023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We show here that the endogenous sphingosine 1-phosphate 5 receptor (S1P(5), a G protein coupled receptor (GPCR) whose natural ligand is sphingosine 1-phosphate (S1P)) and sphingosine kinases 1 and 2 (SK1 and SK2), which catalyse formation of SIP, are co-localised in the centrosome of mammalian cells, where they may participate in regulating mitosis. The centrosome is a site for active GTP-GDP cycling involving the G-protein, G(i) and tubulin, which are required for spindle pole organization and force generation during cell division. Therefore, the presence of S1P(5) (which normally functions as a plasma membrane guanine nucleotide exchange factor, GEF) and sphingosine kinases in the centrosome might suggest that S1P(5) may function as a ligand activated GEF in regulating G-protein-dependent spindle formation and mitosis. The addition of SIP to cells inhibits trafficking of S1P(5) to the centrosome, suggesting a dynamic shuttling endocytic mechanism controlled by ligand occupancy of cell surface receptor. We therefore propose that the centrosomal S1P(5) receptor might function as an intracellular target of SIP linked to regulation of mitosis. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:675 / 684
页数:10
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