Rapamycin reduces VEGF expression in retinal pigment epithelium (RPE) and inhibits RPE-induced sprouting angiogenesis in vitro

被引:63
|
作者
Stahl, A. [1 ]
Paschek, L. [1 ]
Martin, G. [1 ]
Gross, N. J. [1 ]
Feltgen, N. [1 ]
Hansen, L. L. [1 ]
Agostini, H. T. [1 ]
机构
[1] Univ Eye Hosp Freiburg, Cell Biol Lab, D-79106 Freiburg, Germany
关键词
angiogenesis; spheroid; RPE; endothelial; CNV; rapamycin;
D O I
10.1016/j.febslet.2008.08.005
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
Anti-VEGF treatment has become accepted first-line treatment for choroidal neovascularisation (CNV) in age-related macular degeneration. However, VEGF-inhibition does not always lead to sustained CNV-reduction. In this study, the effect of rapamycin was superior to VEGF-inhibition in a co-culture assay of endothelial cells (ECs) and retinal pigment epithelium (RPE). Rapamycin reduced EC sprouting in groups that did not respond to anti-VEGF treatment. Rapamycin did not induce EC apoptosis, but reduced both VEGF-production in RPE and the responsiveness of ECs to stimulation. Rapamycin might therefore be a therapeutic option for CNV patients that do not respond sufficiently to the established anti-VEGF treatments. (C) 2008 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:3097 / 3102
页数:6
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