An update on the biology of sphingosine 1-phosphate receptors

被引:418
作者
Blaho, Victoria A. [1 ]
Hla, Timothy [1 ]
机构
[1] Weill Cornell Med Coll, Ctr Vasc Biol, Dept Pathol & Lab Med, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
immunity; endothelium; vascular permeability; nervous system; migration; activation; immune cells; PROTEIN-COUPLED RECEPTOR; SPHINGOSINE-1-PHOSPHATE TRANSPORTER SPNS2; SIGNAL-REGULATED KINASE-1/2; VASCULAR ENDOTHELIAL-CELLS; BREAST-CANCER CELLS; ZONE B-CELLS; LYMPHOCYTE EGRESS; FINGOLIMOD FTY720; DENDRITIC CELLS; T-CELLS;
D O I
10.1194/jlr.R046300
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
Sphingosine 1-phosphate (S1P) is a membrane-derived lysophospholipid that acts primarily as an extracellular signaling molecule. Signals initiated by S1P are transduced by five G protein-coupled receptors, named S1P(1-5). Cellular and temporal expression of the S1P receptors (S1PRs) determine their specific roles in various organ systems, but they are particularly critical for regulation of the cardiovascular, immune, and nervous systems, with the most well-known contributions of S1PR signaling being modulation of vascular barrier function, vascular tone, and regulation of lymphocyte trafficking. However, our knowledge of S1PR biology is rapidly increasing as they become attractive therapeutic targets in several diseases, such as chronic inflammatory pathologies, autoimmunity, and cancer. Understanding how the S1PRs regulate interactions between biological systems will allow for greater efficacy in this novel therapeutic strategy as well as characterization of complex physiological networks. Because of the rapidly expanding body of research, this review will focus on the most recent advances in S1PRs.
引用
收藏
页码:1596 / 1608
页数:13
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