SREBP inhibits VEGF expression in human smooth muscle cells

被引:21
作者
Motoyama, K
Fukumoto, S [1 ]
Koyama, H
Emoto, M
Shimano, H
Maemura, K
Nishizawa, Y
机构
[1] Osaka City Univ, Grad Sch Med, Osaka 558, Japan
[2] Univ Tsukuba, Inst Clin Med, Dept Internal Med, Tsukuba, Ibaraki 305, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Tokyo, Japan
基金
日本学术振兴会;
关键词
SREBP; VEGF; atherosclerosis; statin; Sp1; transcription; vascular cell;
D O I
10.1016/j.bbrc.2006.01.139
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
Sterol regulatory element-binding proteins (SREBPs) are transcription factors that regulate expression of genes encoding enzymes for lipid biosynthesis. SREBPs are activated by HMG-CoA reductase inhibitors (statins). Statins have been also reported to suppress vascular endothelial growth factor (VEGF) expression in vascular smooth muscle cells (VSMCs). Therefore, we hypothesized that SREBPs are involved in statin-mediated regulation of VEGF production in VSMCs. SREBP1 was robustly expressed, and was activated by atorvastatin in VSMCs, as demonstrated by increased levels of the mature nuclear form of SREBP1, and increased promoter activities of a reporter containing sterol regulatory elements by atorvastatin. Moreover, overexpression of SREBP1a dose-dependently suppressed VEGF promoter activity. Site-specific mutation or deletion of the proximal Sp1 sites reduced the inhibitory effects of SREBP1a on VEGF promoter activity. These data demonstrated that SREBP1, activated by atorvastatin, suppressed VEGF expression through the indirect interaction with the proximal tandem Sp1 sites in VSMCs. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:354 / 360
页数:7
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