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晚期糖基化终末产物可溶性受体:从疾病标志物到潜在治疗靶点。

Soluble receptor for advanced glycation end products: from disease marker to potential therapeutic target.

作者信息

Geroldi Diego, Falcone Colomba, Emanuele Enzo

机构信息

Department of Internal Medicine and Medical Therapeutics, IRCCS San Matteo Hospital, Malattie Vascolari e Metaboliche, University of Pavia, Piazzale Golgi 2, 27100 Pavia, Italy.

出版信息

Curr Med Chem. 2006;13(17):1971-8. doi: 10.2174/092986706777585013.

Abstract

The receptor for advanced glycation end products (RAGE) is a cell-bound receptor of the immunoglobulin superfamily which may be activated by a variety of proinflammatory ligands including advanced glycoxidation end products, S100/calgranulins, high mobility group box 1, and amyloid beta-peptide. RAGE has a secretory splice isoform, soluble RAGE (sRAGE), that lacks the transmembrane domain and therefore circulates in plasma. By competing with cell-surface RAGE for ligand binding, sRAGE may contribute to the removal/neutralization of circulating ligands thus functioning as a decoy. Clinical studies have recently shown that higher plasma levels of sRAGE are associated with a reduced risk of coronary artery disease, hypertension, the metabolic syndrome, arthritis and Alzheimer's disease. Increasing the production of plasma sRAGE is therefore considered to be a promising therapeutic target that has the potential to prevent vascular damage and neurodegeneration. This review presents the state of the art in the use of sRAGE as a disease marker and discusses the therapeutic potential of targeting sRAGE for the treatment of inflammation-related diseases such as atherosclerosis, arthritis and Alzheimer's disease.

摘要

晚期糖基化终末产物受体(RAGE)是免疫球蛋白超家族的一种细胞结合受体,它可被多种促炎配体激活,包括晚期糖氧化终产物、S100/钙粒蛋白、高迁移率族蛋白B1和β-淀粉样肽。RAGE有一种分泌性剪接异构体,即可溶性RAGE(sRAGE),它缺乏跨膜结构域,因此在血浆中循环。通过与细胞表面RAGE竞争配体结合,sRAGE可能有助于清除/中和循环中的配体,从而起到诱饵的作用。临床研究最近表明,血浆中sRAGE水平较高与冠状动脉疾病、高血压、代谢综合征、关节炎和阿尔茨海默病的风险降低有关。因此,提高血浆sRAGE的产生被认为是一个有前景的治疗靶点,有可能预防血管损伤和神经退行性变。本文综述了sRAGE作为疾病标志物的应用现状,并讨论了针对sRAGE治疗动脉粥样硬化、关节炎和阿尔茨海默病等炎症相关疾病的治疗潜力。

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