Structural and functional characteristics of S1P receptors

被引:405
作者
Sanchez, T [1 ]
Hla, T [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Ctr Vasc Biol, Dept Cell Biol, Farmington, CT 06030 USA
关键词
Rho GTPases; migration; vascular maturation; vascular permeability; sphingosine kinase;
D O I
10.1002/jcb.20127
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
The sphingosine-1-phosphate (SIP) family of G protein-coupled receptors (GPCR) regulates essential cellular processes Such as proliferation, migration, cytoskeletal organization, adherens junction assembly, and morphogenesis. SIP, a product from the breakdown of sphingomyelin, binds to the five members of this receptor family, S1P(1), S1P(2), S1P(3), S1P(4), and S1P(5), previously referred to as endothelial differentiation gene (EDG)-1, -5, -3, -6, and -8. SIP receptors are widely expressed in different tissues, so it is not surprising that the SI P receptor family regulates many physiological processes, such as vascular maturation, cardiac development, lymphocyte trafficking, and vascular permeability. FTY720, a new S1P receptor agonist, is undergoing clinical trials as an immunosuppressor. Understanding the physiological role of these receptors and the basics of the ligand-receptor interaction will potentially provide new therapies to control a variety of diseases. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:913 / 922
页数:10
相关论文
共 71 条
  • [1] G-protein-coupled receptor S1P1 acts within endothelial cells to regulate vascular maturation
    Allende, ML
    Yamashita, T
    Proia, RL
    [J]. BLOOD, 2003, 102 (10) : 3665 - 3667
  • [2] Differential pharmacological properties and signal transduction of the sphingosine 1-phosphate receptors EDG-1, EDG-3, and EDG-5
    Ancellin, N
    Hla, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) : 18997 - 19002
  • [3] Cardiac transplant vasculopathy
    Aranda, JM
    Hill, J
    [J]. CHEST, 2000, 118 (06) : 1792 - 1800
  • [4] Ligand-dependent inhibition of B16 melanoma cell migration and invasion via endogenous S1P2 G protein-coupled receptor -: Requirement of inhibition of cellular Rac activity
    Arikawa, K
    Takuwa, N
    Yamaguchi, H
    Sugimoto, N
    Kitayama, J
    Nagawa, H
    Takehara, K
    Takuwa, Y
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (35) : 32841 - 32851
  • [5] Phosphorylation of the immunomodulatory drug FTY720 by sphingosine kinases
    Billich, A
    Bornancin, F
    Dévay, P
    Mechtcheriakova, D
    Urtz, N
    Baumruker, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) : 47408 - 47415
  • [6] SPHINGOSINE-1-PHOSPHATE INHIBITS PDGF-INDUCED CHEMOTAXIS OF HUMAN ARTERIAL SMOOTH-MUSCLE CELLS - SPATIAL AND TEMPORAL-MODULATION OF PDGF CHEMOTACTIC SIGNAL-TRANSDUCTION
    BORNFELDT, KE
    GRAVES, LM
    RAINES, EW
    IGARASHI, Y
    WAYMAN, G
    YAMAMURA, S
    YATOMI, Y
    SIDHU, JS
    KREBS, EG
    HAKOMORI, S
    ROSS, R
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 130 (01) : 193 - 206
  • [7] The immune modulator FTY720 targets sphingosine 1-phosphate receptors
    Brinkmann, V
    Davis, MD
    Heise, CE
    Albert, R
    Cottens, S
    Hof, R
    Bruns, C
    Prieschl, E
    Baumruker, T
    Hiestand, P
    Foster, CA
    Zollinger, M
    Lynch, KR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) : 21453 - 21457
  • [8] Candelore MR, 2002, BIOCHEM BIOPH RES CO, V297, P600
  • [9] FTY720, a novel transplantation drug, modulates lymphocyte migratory responses to chemokines
    Chen, S
    Bacon, KB
    Garcia, G
    Liao, R
    Pan, ZK
    Sullivan, SK
    Nakano, H
    Matsuzawa, A
    Brinkmann, V
    Feng, L
    [J]. TRANSPLANTATION PROCEEDINGS, 2001, 33 (7-8) : 3057 - 3063
  • [10] Synthesis of para-alkyl aryl amide analogues of sphingosine-1-phosphate:: Discovery of potent S1P receptor agonists
    Clemens, JJ
    Davis, MD
    Lynch, KR
    Macdonald, TL
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (20) : 3401 - 3404