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Peroxisome proliferator-activated receptor-γ agonists increase vascular endothelial growth factor expression in human vascular smooth muscle cells
被引:131
|作者:
Yamakawa, K
Hosoi, M
[1
]
Koyama, H
Tanaka, S
Fukumoto, S
Morii, H
Nishizawa, Y
机构:
[1] Osaka City Univ, Sch Med, Dept Internal Med 2, Osaka 5458586, Japan
[2] Osaka City Gen Hosp, Dept Internal Med, Miyakojima, Osaka 5340021, Japan
关键词:
vascular endothelial growth factor;
troglitazone;
thiazolidinedione;
PPAR;
atherosclerosis;
diabetes mellitus;
D O I:
10.1006/bbrc.2000.2665
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:
Vascular endothelial growth factor (VEGF), expressed in a variety of mesenchymal cells including vascular smooth muscle cells (VSMC), is a potent mitogen for endothelial cells, and is used clinically applied for ischemic disease of peripheral vessels. To determine whether peroxisome proliferator-activated receptor gamma (PPAR gamma) regulates VEGF production in VSMC, we examined VEGF secretion from VSMC treated with PPAR agonists. Troglitazone increased VEGF secretion in a time- and dose-dependent manner (261 +/- 35% with 25 mM of troglitazone for 24 h), and also increased levels of VEGF mRNA. VEGF secretion was also increased by other PPAR gamma agonists, pioglitazone, LY171883, and 15d-PGJ2 (224 +/- 17.1%, 247 +/- 36.8% and 171 +/- 7.8%, respectively), but not the PPAR gamma agonists bezafibrate and Wy14643 (85.2 +/- 1.5%, 94.6 +/- 3.2, respectively). Our findings suggest that thiazolidinediones might be useful for the therapeutic angiogenesis for ischemic artery disease. (C) 2000 Academic Press.
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页码:571 / 574
页数:4
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