Chuah Yaw Kuang, Basir Rusliza, Talib Herni, Tie Tung Hing, Nordin Norshariza
Department of Human Anatomy, Faculty of Medicine and Health Sciences, University Putra Malaysia, 43400 Serdang, Selangor, Malaysia.
Int J Inflam. 2013;2013:403460. doi: 10.1155/2013/403460. Epub 2013 Sep 11.
The receptor for advanced glycation end products (RAGE) is a transmembrane receptor of the immunoglobulin superfamily, capable of binding a broad repertoire of ligands. RAGE-ligands interaction induces a series of signal transduction cascades and lead to the activation of transcription factor NF-κB as well as increased expression of cytokines, chemokines, and adhesion molecules. These effects endow RAGE with the role in the signal transduction from pathogen substrates to cell activation during the onset and perpetuation of inflammation. RAGE signaling and downstream pathways have been implicated in a wide spectrum of inflammatory-related pathologic conditions such as arteriosclerosis, Alzheimer's disease, arthritis, acute respiratory failure, and sepsis. Despite the significant progress in other RAGE studies, the functional importance of the receptor in clinical situations and inflammatory diseases still remains to be fully realized. In this review, we will summarize current understandings and lines of evidence on the molecular mechanisms through which RAGE signaling contributes to the pathogenesis of the aforementioned inflammation-associated conditions.
晚期糖基化终末产物受体(RAGE)是免疫球蛋白超家族的一种跨膜受体,能够结合多种配体。RAGE与配体的相互作用会引发一系列信号转导级联反应,导致转录因子NF-κB的激活以及细胞因子、趋化因子和黏附分子表达的增加。这些效应使RAGE在炎症发生和持续过程中,从病原体底物到细胞激活的信号转导中发挥作用。RAGE信号传导及其下游途径与多种炎症相关病理状况有关,如动脉粥样硬化、阿尔茨海默病、关节炎、急性呼吸衰竭和脓毒症。尽管在其他RAGE研究方面取得了重大进展,但该受体在临床情况和炎症性疾病中的功能重要性仍有待充分认识。在本综述中,我们将总结目前关于RAGE信号传导促成上述炎症相关病症发病机制的分子机制的理解和证据。