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RAGE 介导体炎症、2 型糖尿病和糖尿病血管并发症。

RAGE-Mediated Inflammation, Type 2 Diabetes, and Diabetic Vascular Complication.

机构信息

Department of Biochemistry and Molecular Vascular Biology, Kanazawa University Graduate School of Medical Sciences , Kanazawa , Japan.

出版信息

Front Endocrinol (Lausanne). 2013 Aug 21;4:105. doi: 10.3389/fendo.2013.00105. eCollection 2013.

Abstract

Obesity is associated with inflammation and type 2 diabetes. Innate immune system comprised of cellular and molecular components plays an important role in the inflammatory reactions. Immune cells like macrophages and their cell surface pattern-recognition receptors (PRRs) are representative for innate immunity promoting inflammatory reactions. The receptor for advanced glycation end-products (RAGE) is a member of PRRs and a proinflammatory molecular device that mediates danger signals to the body. The expression of RAGE is observed in adipocytes as well as immune cells, endothelial cells, and pancreatic β cells under certain conditions. It has been reported that RAGE is implicated in adipocyte hypertrophy and insulin resistance. RAGE-mediated regulation of adiposity and inflammation may attribute to type 2 diabetes and diabetic vascular complications.

摘要

肥胖与炎症和 2 型糖尿病有关。先天免疫系统由细胞和分子组成部分组成,在炎症反应中起着重要作用。免疫细胞如巨噬细胞及其细胞表面模式识别受体 (PRRs) 是促进炎症反应的先天免疫的代表。晚期糖基化终产物 (RAGE) 受体是 PRRs 的成员,也是一种促炎分子装置,可将危险信号传递给身体。在某些情况下,RAGE 在脂肪细胞以及免疫细胞、内皮细胞和胰岛 β 细胞中表达。据报道,RAGE 参与脂肪细胞肥大和胰岛素抵抗。RAGE 介导的脂肪量和炎症调节可能导致 2 型糖尿病和糖尿病血管并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3a1/3748367/5421c45b27ec/fendo-04-00105-g001.jpg

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