Sphingosine 1-phosphate and lysophosphatidic acid receptors: agonist and antagonist binding and progress toward development of receptor-specific ligands

被引:35
作者
Parrill, AL [1 ]
Sardar, VM
Yuan, HB
机构
[1] Memphis State Univ, Dept Chem, Memphis, TN 38152 USA
[2] Memphis State Univ, Computat Res Mat Inst, Memphis, TN 38152 USA
关键词
computational model; lysophosphatidic acid; receptor structure; sphingosine; 1-phosphate; structure activity relationship;
D O I
10.1016/j.semcdb.2004.05.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sphingosine 1-phosphate and lysophosphatidic acid are two phospholipid growth factors whose importance in physiology and pathophysiology is becoming more and more apparent. Structure-activity relationships for agonism and antagonism at the thirteen known cell-surface and one intracellular receptor are described. Particular emphasis is placed on ligands having different selectivity than the parent molecules. Structural insights regarding agonist and antagonist recognition by the receptors from both computational modeling studies and crystallography are also discussed. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:467 / 476
页数:10
相关论文
共 108 条
  • [11] Bittman R, 1996, J LIPID RES, V37, P391
  • [12] 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
  • [13] FTY720: targeting G-protein-coupled receptors for sphingosine 1-phosphate in transplantation and autoimmunity
    Brinkmann, V
    Lynch, KR
    [J]. CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (05) : 569 - 575
  • [14] FTY720: Altered lymphocyte traffic results in allograft protection.
    Brinkmann, V
    Pinschewer, DD
    Feng, L
    Chen, S
    [J]. TRANSPLANTATION, 2001, 72 (05) : 764 - 769
  • [15] Chiba K, 1998, J IMMUNOL, V160, P5037
  • [16] 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
  • [17] Central role of peroxisome proliferator-activated receptors in the actions of peroxisome proliferators
    Corton, JC
    Anderson, SP
    Stauber, A
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2000, 40 : 491 - 518
  • [18] Structure of the PPARα and -γ ligand binding domain in complex with AZ 242;: Ligand selectivity and agonist activation in the PPAR family
    Cronet, P
    Petersen, JFW
    Folmer, R
    Blomberg, N
    Sjöblom, K
    Karlsson, U
    Lindstedt, EL
    Bamberg, K
    [J]. STRUCTURE, 2001, 9 (08) : 699 - 706
  • [19] Oxidized alkyl phospholipids are specific, high affinity peroxisome proliferator-activated receptor γ ligands and agonists
    Davies, SS
    Pontsler, AV
    Marathe, GK
    Harrison, KA
    Murphy, RC
    Hinshaw, JC
    Prestwich, GD
    St Hilaire, A
    Prescott, SM
    Zimmerman, GA
    McIntyre, TM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (19) : 16015 - 16023
  • [20] LPA protects intestinal epithelial cells from apoptosis by inhibiting the mitochondrial pathway
    Deng, WL
    Wang, D
    Gosmanova, E
    Johnson, LR
    Tigyi, G
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 284 (05): : G821 - G829