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RAGE 在炎症及其他方面的调控和信号转导。

RAGE regulation and signaling in inflammation and beyond.

机构信息

Department of Neuropathology, University of Freiburg, Freiburg, Germany.

出版信息

J Leukoc Biol. 2013 Jul;94(1):55-68. doi: 10.1189/jlb.1012519. Epub 2013 Mar 29.

Abstract

RAGE is a key molecule in the onset and sustainment of the inflammatory response. New studies indicate that RAGE might represent a new link between the innate and adaptive immune system. RAGE belongs to the superfamily of Ig cell-surface receptors and is expressed on all types of leukocytes promoting activation, migration, or maturation of the different cells. RAGE expression is prominent on the activated endothelium, where it mediates leukocyte adhesion and transmigration. Moreover, proinflammatory molecules released from the inflamed or injured vascular system induce migration and proliferation of SMCs. RAGE binds a large number of different ligands and is therefore considered as a PRR, recognizing a structural motif rather than a specific ligand. In this review, we summarize the current knowledge about the signaling pathways activated in the different cell types and discuss a potential activation mechanism of RAGE, as well as putative options for therapeutic intervention.

摘要

RAGE 是炎症反应发生和持续的关键分子。新的研究表明,RAGE 可能代表先天免疫和适应性免疫系统之间的新联系。RAGE 属于 Ig 细胞表面受体超家族,在所有类型的白细胞上表达,促进不同细胞的激活、迁移或成熟。RAGE 表达在上皮细胞激活时更为明显,介导白细胞黏附和迁移。此外,从炎症或受损的血管系统释放的促炎分子诱导平滑肌细胞的迁移和增殖。RAGE 结合大量不同的配体,因此被认为是一种 PRR,识别结构基序而不是特定的配体。在这篇综述中,我们总结了目前关于不同细胞类型中激活的信号通路的知识,并讨论了 RAGE 的潜在激活机制以及潜在的治疗干预选择。

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