Vascular endothelial growth factor upregulates pigment epithelium-derived factor expression via VEGFR-1 in human retinal pigment epithelial cells

被引:91
作者
Ohno-Matsui, K
Yoshida, T
Uetama, T
Mochizuki, M
Morita, I
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Dept Ophthalmol & Visual Sci, Bunkyo Ku, Tokyo 1138519, Japan
[2] Tokyo Med & Dent Univ, Grad Sch, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138519, Japan
基金
日本学术振兴会;
关键词
retinal pigment epithelium; age-related macular degeneration; VEGF; PEDF; choroidal neovascularization; VEGFR-1;
D O I
10.1016/S0006-291X(03)00446-7
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
We previously demonstrated that differentiated retinal pigment epithelial (RPE) cells express high levels of vascular endothelial growth factor (VEGF) and pigment epithelium-derived factor (PEDF), and a critical balance between VEGF and PEDF is important to prevent the development of choroidal neovascularization. We report here that VEGF secreted by RPE cells upregulates PEDF expression via VEGFR-1 in an autocrine manner. PEDF mRNA and protein expression was downregulated by neutralizing antibody against VEGF in differentiated human RPE cells. VEGFR-1 neutralization decreased PEDF mRNA and protein expression whereas anti-VEGFR-2 antibody had no effect. Addition of placenta growth factor (PIGF) restored PEDF expression in the presence of anti-VEGF antibody. These results demonstrate a regulatory interaction between angiogenesis stimulators and inhibitors to maintain homeostasis in normal human retina. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:962 / 967
页数:6
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