The advanced glycation endproduct pentosidine induces the expression of PDGF-B in human retinal pigment epithelial cells

被引:57
作者
Handa, JT
Reiser, KM
Matsunaga, H
Hjelmeland, LM
机构
[1] Univ Calif Davis, Sch Med, Vitreoretinal Res Lab, Dept Ophthalmol, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept CRPRC, Davis, CA USA
[3] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA USA
关键词
advanced glycation endproduct (AGE); nonenzymatic glycation; pentosidine; platelet-derived growth factor (PDGF); retinal pigment epithelium (RPE);
D O I
10.1006/exer.1997.0442
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Advanced glycation endproducts have been implicated in a number of diabetic and aging changes. Some of these effects occur in part through induction of cytokines such as platelet-derived growth factor (PDGF), which is expressed by the retinal pigment epithelium (RPE). In this study, cultures of RPE were evaluated for PDGF expression after treatment with pentosidine, a well characterized advanced glycation endproduct. Northern analysis provided evidence for the increased expression of a 3.7 kb PDGF-B transcript over unstimulated controls in the established ARPE-19 cell line. Western analysis demonstrated increased PDGF-BB protein in conditioned medium compared to controls of ARPE-19 cells. In addition, two different early passage cultures of RPE showed increased PDGF-BB protein after pentosidine treatment compared to unstimulated controls. The enhanced production of PDGF-BB could play a role in the maintenance of the RPE-Bruch's membrane complex and influence changes associated with diabetes and aging. (C) 1998 Academic Press Limited.
引用
收藏
页码:411 / 419
页数:9
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