Advanced glycation end products and RAGE: a common thread in aging, diabetes, neurodegeneration, and inflammation

被引:644
作者
Ramasamy, R
Vannucci, SJ
Yan, SSD
Herold, K
Yan, SF
Schmidt, AM [1 ]
机构
[1] Columbia Univ, Med Ctr, Dept Surg, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Dept Pediat, New York, NY 10032 USA
[3] Columbia Univ, Med Ctr, Dept Med, New York, NY 10032 USA
[4] Columbia Univ, Med Ctr, Dept Pathol, New York, NY 10032 USA
关键词
age; glucose; injury; oxidative stress; receptors;
D O I
10.1093/glycob/cwi053
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 products of nonenzymatic glycation and oxidation of proteins and lipids, the advanced glycation end products (AGEs), accumulate in a wide variety of environments. AGEs may be generated rapidly or over long times stimulated by a range of distinct triggering mechanisms, thereby accounting for their roles in multiple settings and disease states. A critical property of AGEs is their ability to activate receptor for advanced glycation end products (RAGE), a signal transduction receptor of the immunoglobulin superfamily. It is our hypothesis that due to such interaction, AGEs impart a potent impact in tissues, stimulating processes linked to inflammation and its consequences. We hypothesize that AGEs cause perturbation in a diverse group of diseases, such as diabetes, inflammation, neurodegeneration, and aging. Thus, we propose that targeting this pathway may represent a logical step in the prevention/treatment of the sequelae of these disorders.
引用
收藏
页码:16R / 28R
页数:13
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