Blockade of receptor for advanced glycation endproducts: a new target for therapeutic intervention in diabetic complications and inflammatory disorders

被引:145
作者
Hudson, BI [1 ]
Bucciarelli, LG
Wendt, T
Sakaguchi, T
Lalla, E
Qu, W
Lu, Y
Lee, L
Stern, DM
Naka, Y
Ramasamy, R
Yan, SD
Yan, SF
D'Agati, V
Schmidt, AM
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Surg, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[4] Med Coll Georgia, Deans Off, Augusta, GA 30912 USA
关键词
glycation; oxidation; receptors; RAGE; diabetes; inflammation;
D O I
10.1016/j.abb.2003.08.030
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
The glycation and oxidation of proteins/lipids leads to the generation of a new class of biologically active moieties, the advanced glycation endproducts (AGEs). Recent studies have elucidated that carboxymethyllysine (CML) adducts of proteins/lipids are a highly prevalent AGE in vivo. CML-modified adducts are signal transduction ligands of the receptor for AGE (RAGE), a member of the immunoglobulin superfamily. Importantly, CML-modified adducts accumulate in diverse settings. In addition to enhanced formation in settings of high glucose, these adducts form in inflammatory milieu. Studies performed both in vitro and it) vivo have suggested that the proinflammatory/tissue destructive consequences of RAGE activation in the diabetic/inflamed environment may be markedly attenuated by blockade of the ligand-RAGE axis. Here, we will summarize the known consequences of RAGE activation in the tissues and highlight novel areas for therapeutic intervention in these disease states. (C) 2003 Published by Elsevier Inc.
引用
收藏
页码:80 / 88
页数:9
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