RAGE in tissue homeostasis, repair and regeneration

被引:175
|
作者
Sorci, Guglielmo [1 ,2 ]
Riuzzi, Francesca [1 ,2 ]
Giambanco, Ileana [1 ]
Donato, Rosario [1 ,2 ]
机构
[1] Univ Perugia, Dept Expt Med & Biochem Sci, I-06122 Perugia, Italy
[2] Univ Perugia, Interuniv Inst Myol, I-06122 Perugia, Italy
来源
关键词
RAGE; Inflammation; Cancer; Tissue regeneration/repair; HMGB1; S100; protein; GLYCATION END-PRODUCTS; NEURITE OUTGROWTH; ENDPRODUCTS RAGE; MICROGLIAL RECEPTOR; ALZHEIMERS-DISEASE; CYTOPLASMIC DOMAIN; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; SINGLE RECEPTOR; CELL-MIGRATION;
D O I
10.1016/j.bbamcr.2012.10.021
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
RAGE (receptor for advanced glycation end-products) is a multiligand receptor of the immunoglobulin superfamily involved in inflammation, diabetes, atherosclerosis, nephropathy, neurodegeneration, and cancer. Advanced glycation end-products, high mobility group box-1 (amphoterin), beta-amyloid fibrils, certain S100 proteins, and DNA and RNA are RAGE ligands. Upon RAGE ligation, adaptor proteins (i.e., diaphanous-1, TIRAP, MyD88 and/or other as yet unidentified adaptors) associate with RAGE cytoplasmic domain resulting in signaling. However, RAGE activation may not be restricted to pathological statuses, the receptor being involved in tissue homeostasis and regeneration/repair upon acute injury, and in resolution of inflammation. RAGE effects are strongly dependent on the cell type and the context, which may condition therapeutic strategies aimed at reducing RAGE signaling. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 109
页数:9
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