Lysophospholipids and the cardiovascular system

被引:70
作者
Karliner, JS [1 ]
机构
[1] Univ Calif San Francisco, Vet Adm Med Ctr 111C, San Francisco, CA 94121 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2002年 / 1582卷 / 1-3期
关键词
sphingosine-1-phosphate; vascular development; cardioprotection; lysophosphatidic acid; atherosclerosis; G-protein-coupled receptors; ischemia/reperfusion;
D O I
10.1016/S1388-1981(02)00174-9
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 lysophospholipids sphingosine-1-phosphate (S1P) and lysophosphatidic acid (LPA) have varied effects on the cardiovascular system. S1P is necessary for normal vascular development and may play an important role in angiogenesis. These molecules may exert potentially detrimental effects. Both S1P and LPA are released from activated platelets and can in turn stimulate platelet aggregation. These thrombogenic effects would further enhance ischemia in acute coronary syndromes and myocardial infarction. LPA is a major component of the lipid core of human atherosclerotic plaques and can stimulate vascular smooth muscle proliferation. Both LPA and S1P cause cardiac myocyte hypertrophy in vitro. Beneficial effects include cardioprotection both in vitro and during ischemia/reperfusion in an ex vivo whole heart mouse model. Understanding both the acute and the chronic physiologic and pathophysiologic roles of the lysophospholipids and their cognate receptors and signaling pathways in the cardiovascular system, which are likely to be species-, tissue-, and cell-specific, may allow the development of molecules that can be targeted to stimulate or inhibit a specific function. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:216 / 221
页数:6
相关论文
共 60 条
[1]  
ALTER M, 1994, STROKE, V25, P1141
[2]   Sphingosine 1-phosphate-induced cell proliferation, survival, and related signaling events mediated by G protein-coupled receptors Edg3 and Edg5 [J].
An, SZ ;
Zheng, YH ;
Bleu, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) :288-296
[3]   GM1 GANGLIOSIDE THERAPY IN ACUTE ISCHEMIC STROKE [J].
ARGENTINO, C ;
SACCHETTI, ML ;
TONI, D ;
SAVOINI, G ;
DARCANGELO, E ;
ERMINIO, F ;
FEDERICO, F ;
MILONE, FF ;
GALLAI, V ;
GAMBI, D ;
MAMOLI, A ;
OTTONELLO, GA ;
PONARI, O ;
REBUCCI, G ;
SENIN, U ;
FIESCHI, C .
STROKE, 1989, 20 (09) :1143-1149
[4]   Role of sphingosine 1-phosphate in the mitogenesis induced by oxidized low density lipoprotein in smooth muscle cells via activation of sphingomyelinase, ceramidase, and sphingosine kinase [J].
Augé, N ;
Nikolova-Karakashian, M ;
Carpentier, S ;
Parthasarathy, S ;
Négre-Salvayre, A ;
Salvayre, R ;
Merrill, AH ;
Levade, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (31) :21533-21538
[5]   Sphingosine-1-phosphate reduces rat renal and mesenteric blood flow in vivo in a pertussis toxin-sensitive manner [J].
Bischoff, A ;
Czyborra, P ;
Heringdorf, DMZ ;
Jakobs, KH ;
Michel, MC .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 130 (08) :1878-1883
[6]  
Bunemann M, 1995, J PHYSIOL-LONDON, V489, P701
[7]   A novel membrane receptor with high affinity for lysosphingomyelin and sphingosine 1-phosphate in atrial myocytes [J].
Bunemann, M ;
Liliom, K ;
Brandts, BK ;
Pott, L ;
Tseng, JL ;
Desiderio, DM ;
Sun, GP ;
Miller, D ;
Tigyi, G .
EMBO JOURNAL, 1996, 15 (20) :5527-5534
[8]   Ganglioside GM1 protection from apoptosis of rat heart fibroblasts [J].
Cavallini, L ;
Venerando, R ;
Miotto, G ;
Alexandre, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1999, 370 (02) :156-162
[9]   Suppression of ceramide-mediated programmed cell death by sphingosine-1-phosphate [J].
Cuvillier, O ;
Pirianov, G ;
Kleuser, B ;
Vanek, PG ;
Coso, OA ;
Gutkind, JS ;
Spiegel, S .
NATURE, 1996, 381 (6585) :800-803
[10]  
Edsall LC, 1997, J NEUROSCI, V17, P6952