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pubmed-article:9593635pubmed:abstractTextAdvanced 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.lld:pubmed
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pubmed-article:9593635pubmed:authorpubmed-author:ReiserK MKMlld:pubmed
pubmed-article:9593635pubmed:authorpubmed-author:MatsunagaHHlld:pubmed
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pubmed-article:9593635pubmed:authorpubmed-author:HandaJ TJTlld:pubmed
pubmed-article:9593635pubmed:copyrightInfoCopyright 1998 Academic Press Limited.lld:pubmed
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pubmed-article:9593635pubmed:volume66lld:pubmed
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pubmed-article:9593635pubmed:pagination411-9lld:pubmed
pubmed-article:9593635pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:9593635pubmed:articleTitleThe advanced glycation endproduct pentosidine induces the expression of PDGF-B in human retinal pigment epithelial cells.lld:pubmed
pubmed-article:9593635pubmed:affiliationDepartment of Ophthalmology, University of California, Davis, CA 95616-8794, USA.lld:pubmed
pubmed-article:9593635pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9593635pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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