Suppr超能文献

靶向 RAGE 信号在炎症性疾病中的作用。

Targeting RAGE Signaling in Inflammatory Disease.

机构信息

Department of Cell Biology, Leonard M. Miller School of Medicine, University of Miami, Miami, Florida 33136, USA; email:

University of Miami Sylvester Comprehensive Cancer Center, Miami, Florida 33136, USA.

出版信息

Annu Rev Med. 2018 Jan 29;69:349-364. doi: 10.1146/annurev-med-041316-085215. Epub 2017 Nov 6.

Abstract

The receptor for advanced glycation end-products (RAGE) is a multiligand pattern recognition receptor implicated in diverse chronic inflammatory states. RAGE binds and mediates the cellular response to a range of damage-associated molecular pattern molecules (DAMPs) including AGEs, HMGB1, S100s, and DNA. RAGE can also act as an innate immune sensor of microbial pathogen-associated molecular pattern molecules (PAMPs) including bacterial endotoxin, respiratory viruses, and microbial DNA. RAGE is expressed at low levels under normal physiology, but it is highly upregulated under chronic inflammation because of the accumulation of various RAGE ligands. Blocking RAGE signaling in cell and animal models has revealed that targeting RAGE impairs inflammation and progression of diabetic vascular complications, cardiovascular disease (CVD), and cancer progression and metastasis. The clinical relevance of RAGE in inflammatory disease is being demonstrated in emerging clinical trials of novel small-molecule RAGE inhibitors.

摘要

晚期糖基化终产物受体(RAGE)是一种多配体模式识别受体,与多种慢性炎症状态有关。RAGE 结合并介导细胞对一系列损伤相关分子模式分子(DAMPs)的反应,包括 AGEs、HMGB1、S100 蛋白和 DNA。RAGE 还可以作为微生物病原体相关分子模式分子(PAMPs)的先天免疫传感器,包括细菌内毒素、呼吸道病毒和微生物 DNA。在正常生理条件下,RAGE 的表达水平较低,但由于各种 RAGE 配体的积累,在慢性炎症下其表达水平会显著上调。在细胞和动物模型中阻断 RAGE 信号通路已表明,靶向 RAGE 可损害糖尿病血管并发症、心血管疾病(CVD)以及癌症进展和转移的炎症和进展。在新型小分子 RAGE 抑制剂的新兴临床试验中,正在证明 RAGE 在炎症性疾病中的临床相关性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验