Sphingosine 1-phosphate receptors

被引:112
作者
Hla, T [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Physiol, Ctr Vasc Biol, Farmington, CT 06030 USA
来源
PROSTAGLANDINS & OTHER LIPID MEDIATORS | 2001年 / 64卷 / 1-4期
关键词
D O I
10.1016/S0090-6980(01)00109-5
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 (SPP) is a bioactive lipid produced from the metabolism of sphingomyelin. It is an important constituent of serum and regulates cell growth, survival, migration, differentiation and gene expression. Its mode of action has been enigmatic; however, recent findings have shown that a family of G-protein-coupled receptors (GPCR) of the endothelial differentiation gene (EDG) family serve as plasma membrane-localized receptors for SPP. Furthermore, the EDG receptors appear to be SPP receptor subtypes with distinct signaling characteristics. In vascular endothelial cells, SPP acts on EDG-1 and EDG-3 subtypes of receptors to induce cell survival and morphogenesis. Such pathways appear to be critical for SPP-induced angiogenic response in vivo. In addition, the EDG-1 gene is essential for vascular maturation in development. Moreover, developmental studies in Zebrafish have indicated that SPP signaling via the EDG-5 like receptor Miles Apart (Mil) is essential for heart development. These data strongly suggest that a physiological role of SPP is in the formation of the cardiovascular system. Despite these recent findings, much needs to be clarified with respect to the physiological role of SPP synthesis and action. This review will focus on the recent findings on SPP receptors and the effects on the cardiovascular system. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:135 / 142
页数:8
相关论文
共 47 条
  • [1] Identification of cDNAs encoding two G protein-coupled receptors for lysosphingolipids
    An, SZ
    Bleu, T
    Huang, W
    Hallmark, OG
    Coughlin, SR
    Goetzl, EJ
    [J]. FEBS LETTERS, 1997, 417 (03) : 279 - 282
  • [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] Edsall LC, 1997, J NEUROSCI, V17, P6952
  • [4] Molecular cloning and characterization of a human mitochondrial ceramidase
    El Bawab, S
    Roddy, P
    Qian, T
    Bielawska, A
    Lemasters, JJ
    Hannun, YA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (28) : 21508 - 21513
  • [5] The novel sphingosine 1-phosphate receptor AGR16 is coupled via pertussis toxin-sensitive and -insensitive G-proteins to multiple signalling pathways
    Gonda, K
    Okamoto, H
    Takuwa, N
    Yatomi, Y
    Okazaki, H
    Sakurai, T
    Kimura, S
    Sillard, R
    Harii, K
    Takuwa, Y
    [J]. BIOCHEMICAL JOURNAL, 1999, 337 : 67 - 75
  • [6] LYSOSPHINGOLIPIDS INHIBIT PROTEIN-KINASE-C - IMPLICATIONS FOR THE SPHINGOLIPIDOSES
    HANNUN, YA
    BELL, RM
    [J]. SCIENCE, 1987, 235 (4789) : 670 - 674
  • [7] FUNCTIONS OF SPHINGOLIPIDS AND SPHINGOLIPID BREAKDOWN PRODUCTS IN CELLULAR-REGULATION
    HANNUN, YA
    BELL, RM
    [J]. SCIENCE, 1989, 243 (4890) : 500 - 507
  • [8] Hla T, 1999, BIOCHEM PHARMACOL, V58, P201
  • [9] Characterization of a novel sphingosine 1-phosphate receptor, Edg-8
    Im, DS
    Heise, CE
    Ancellin, N
    O'Dowd, BF
    Shei, GJ
    Heavens, RP
    Rigby, MR
    Hla, T
    Mandala, S
    McAllister, G
    George, SR
    Lynch, KR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (19) : 14281 - 14286
  • [10] Signaling to Rho GTPases
    Kjoller, L
    Hall, A
    [J]. EXPERIMENTAL CELL RESEARCH, 1999, 253 (01) : 166 - 179