Relationship of molecular structure to the mechanism of lysophospholipid-induced smooth muscle cell proliferation

被引:19
作者
Chai, YC [1 ]
Binion, DG [1 ]
Chisolm, GM [1 ]
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Cell Biol, Cleveland, OH 44195 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2000年 / 279卷 / 04期
关键词
basic fibroblast growth factor; lysophosphatidylcholine; lysophosphatidic acid; platelet-activating factor; vitamin E;
D O I
10.1152/ajpheart.2000.279.4.H1830
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We previously reported that oxidized low-density lipoprotein and one of its constituents, lysophosphatidylcholine (lysoPC), caused smooth muscle cell proliferation that was inhibitable by vitamin E and by a neutralizing antibody against basic fibroblast growth factor-2 (FGF-2). We now show that the mitogenic activity of lysolipids is highly dependent on structure. Phospholipids with palmitoyl fatty acid and phosphocholine induced DNA synthesis optimally. Shorter and longer fatty acids were significantly less potent, as were phosphoserine and phosphoethanolamine head groups. Structurally related phospholipids [platelet-activating factor (PAF) and lysoPAF] were also mitogens and acted via an analogous FGF-2-dependent, vitamin E-inhibitable mechanism. The mechanism of lysoPC stimulation was distinct from that of another phospholipid mitogen, lysophosphatidic acid (lysoPA), in that lysoPC stimulation was not pertussis toxin inhibitable. Furthermore, lysoPA stimulation was not inhibitable by vitamin E. Despite its distinct cellular pathway for stimulation, lysoPA also ultimately led to FGF-2 release. Our data show that specific structural attributes of lysoPC, PAF, and lysoPAF enable these agents to mediate smooth muscle cell release of FGF-2, which in turn stimulates proliferation.
引用
收藏
页码:H1830 / H1838
页数:9
相关论文
共 48 条
[1]   ANGIOTENSIN INCREASES CYTOSOLIC FREE CALCIUM IN CULTURED VASCULAR SMOOTH-MUSCLE CELLS [J].
BROCK, TA ;
ALEXANDER, RW ;
EKSTEIN, LS ;
ATKINSON, WJ ;
GIMBRONE, MA .
HYPERTENSION, 1985, 7 (03) :I105-I109
[2]   Oxidized low density lipoprotein and lysophosphatidylcholine stimulate cell cycle entry in vascular smooth muscle cells - Evidence for release of fibroblast growth factor-2 [J].
Chai, YC ;
Howe, PH ;
DiCorleto, PE ;
Chisolm, GM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :17791-17797
[3]  
CHATTERJEE S, 1992, MOL CELL BIOCHEM, V111, P143
[4]   LYSOPHOSPHATIDYLCHOLINE CAUSES CA2+ INFLUX, ENHANCED DNA-SYNTHESIS AND CYTOTOXICITY IN CULTURED VASCULAR SMOOTH-MUSCLE CELLS [J].
CHEN, Y ;
MORIMOTO, S ;
KITANO, S ;
KOH, E ;
FUKUO, K ;
JIANG, B ;
CHEN, S ;
YASUDA, O ;
HIROTANI, A ;
OGIHARA, T .
ATHEROSCLEROSIS, 1995, 112 (01) :69-76
[5]   Induction of DNA synthesis by a single transient mechanical stimulus of human vascular smooth muscle cells - Role of fibroblast growth factor-2 [J].
Cheng, GC ;
Libby, P ;
Grodzinsky, AJ ;
Lee, RT .
CIRCULATION, 1996, 93 (01) :99-105
[6]  
Chisolm GM, 1997, DEV CARDIOVASC MED, P389
[7]  
CHISOLM GM, 1996, ATHEROSCLEROSIS CORO, P129
[8]   Lysophosphatidylcholine regulates cationic amino acid transport and metabolism in vascular smooth muscle cells - Role in polyamine biosynthesis [J].
Durante, W ;
Liao, L ;
Peyton, KJ ;
Schafer, AI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (48) :30154-30159
[9]   Lysophosphatidylcholine stimulates activator protein 1 and the c-Jun N-terminal kinase activity [J].
Fang, XJ ;
Gibson, S ;
Flowers, M ;
Furui, T ;
Bast, RC ;
Mills, GB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (21) :13683-13689
[10]   Molecular cloning of a high-affinity receptor for the growth factor-like lipid mediator lysophosphatidic acid from Xenopus oocytes [J].
Guo, Z ;
Liliom, K ;
Fischer, DJ ;
Bathurst, IC ;
Tomei, LD ;
Kiefer, MC ;
Tigyi, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14367-14372