Sphingosine-1-phosphate receptor 1 signalling in T cells: trafficking and beyond

被引:122
|
作者
Garris, Christopher S. [1 ]
Blaho, Victoria A. [2 ]
Hla, Timothy [2 ]
Han, May H. [3 ]
机构
[1] Harvard Univ, Sch Med, Div Med Sci, Grad Program Immunol, Boston, MA USA
[2] Cornell Univ, Weill Cornell Med Coll, Ctr Vasc Biol, Dept Pathol & Lab Med, New York, NY 10021 USA
[3] Stanford Univ, Dept Neurol & Neurol Sci, Sch Med, Stanford, CA 94305 USA
关键词
immune cells; sphingosine; 1-phosphate; T cells; CENTRAL-NERVOUS-SYSTEM; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; PROTEIN-COUPLED RECEPTOR; ORAL FINGOLIMOD FTY720; SPHINGOSINE; 1-PHOSPHATE; LYMPHOCYTE EGRESS; TGF-BETA; CENTRAL MEMORY; DIFFERENTIATION; S1P(1);
D O I
10.1111/imm.12272
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sphingosine-1-phosphate (S1P) is a lipid second messenger that signals via five G protein-coupled receptors (S1P1-5). S1P receptor (S1PR) signalling is associated with a wide variety of physiological processes including lymphocyte biology, their recirculation and determination of T-cell phenotypes. The effect of FTY720 (Fingolimod, Gilenya) to regulate lymphocyte egress and to ameliorate paralysis in experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis led to the use of FTY720 as a first-line oral agent for treatment of relapsing-remitting multiple sclerosis. However, a significant body of research suggests that S1P signalling may participate in diverse immune regulatory functions other than lymphocyte trafficking. This review article discusses the current knowledge of S1P signalling in the fate and function of T regulatory, T helper type 17 and memory T cells in health and disease.
引用
收藏
页码:347 / 353
页数:7
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