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.
引用
收藏
页码:571 / 574
页数:4
相关论文
共 21 条
[1]   VASCULAR ENDOTHELIAL GROWTH-FACTOR IN OCULAR FLUID OF PATIENTS WITH DIABETIC-RETINOPATHY AND OTHER RETINAL DISORDERS [J].
AIELLO, LP ;
AVERY, RL ;
ARRIGG, PG ;
KEYT, BA ;
JAMPEL, HD ;
SHAH, ST ;
PASQUALE, LR ;
THIEME, H ;
IWAMOTO, MA ;
PARK, JE ;
NGUYEN, HV ;
AIELLO, LM ;
FERRARA, N ;
KING, GL .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (22) :1480-1487
[2]   Vascular permeability in experimental diabetes is associated with reduced endothelial occludin content - Vascular endothelial growth factor decreases occludin in retinal endothelial cells [J].
Antonetti, DA ;
Barber, AJ ;
Khin, S ;
Lieth, E ;
Tarbell, JM ;
Gardner, TW .
DIABETES, 1998, 47 (12) :1953-1959
[3]  
Arroyo MVA, 1998, KIDNEY INT, V54, pS7
[4]   VASCULAR-PERMEABILITY FACTOR (VASCULAR ENDOTHELIAL GROWTH-FACTOR) GENE IS EXPRESSED DIFFERENTIALLY IN NORMAL-TISSUES, MACROPHAGES, AND TUMORS [J].
BERSE, B ;
BROWN, LF ;
VANDEWATER, L ;
DVORAK, HF ;
SENGER, DR .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (02) :211-220
[5]   Immunohistochemical expression of vascular endothelial growth factor vascular permeability factor in atherosclerotic intimas of human coronary arteries [J].
Chen, YX ;
Nakashima, Y ;
Tanaka, K ;
Shiraishi, S ;
Nakagawa, K ;
Sueishi, K .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (01) :131-139
[6]   Protein kinase C delta inhibits the proliferation of vascular smooth muscle cells by suppressing G(1) cyclin expression [J].
Fukumoto, S ;
Nishizawa, Y ;
Hosoi, M ;
Koyama, H ;
Yamakawa, K ;
Ohno, S ;
Morii, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (21) :13816-13822
[7]   Vascular endothelial growth factor (VEGF) expression in human coronary atherosclerotic lesions - Possible pathophysiological significance of VEGF in progression of atherosclerosis [J].
Inoue, M ;
Itoh, H ;
Ueda, M ;
Naruko, T ;
Kojima, A ;
Komatsu, R ;
Doi, K ;
Ogawa, Y ;
Tamura, N ;
Takaya, K ;
Igaki, T ;
Yamashita, J ;
Chun, TH ;
Masatsugu, K ;
Becker, AE ;
Nakao, K .
CIRCULATION, 1998, 98 (20) :2108-2116
[8]   Clinical evidence of angiogenesis after arterial gene transfer of phVEGF(165) in patient with ischaemic limb [J].
Isner, JM ;
Pieczek, A ;
Schainfeld, R ;
Blair, R ;
Haley, L ;
Asahara, T ;
Rosenfield, K ;
Razvi, S ;
Walsh, E ;
Symes, JF .
LANCET, 1996, 348 (9024) :370-374
[9]  
Izumi T, 1996, J PHARMACOL EXP THER, V277, P1630
[10]   Troglitazone enhances glucose uptake and inhibits mitogen-activated protein kinase in human aortic smooth muscle cells [J].
Kihara, S ;
Ouchi, N ;
Funahashi, T ;
Shinohara, E ;
Tamura, R ;
Yamashita, S ;
Matsuzawa, Y .
ATHEROSCLEROSIS, 1998, 136 (01) :163-168