کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1963509 1058458 2013 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The receptor for advanced glycation end-products: A complex signaling scenario for a promiscuous receptor
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
The receptor for advanced glycation end-products: A complex signaling scenario for a promiscuous receptor
چکیده انگلیسی

Firstly described in 1992, the receptor for advanced glycation end-products has attracted increasing attention due to its diverse ligand repertoire and involvement in several pathophysiological processes associated with inflammation such as in diabetes, cancer, autoimmune diseases and neurodegenerative diseases.This receptor in addition to its binding capacity for advanced glycation end-products also recognizes some molecules classified as both, pathogen- and damage-associated molecular patterns and thus triggering the transcription of genes encoding inflammatory mediators. Some of these ligands are common for both, the receptor of advanced glycation end-products and members of the Toll-like receptor family, generating shared signaling cascades. Furthermore, these receptors may cooperate as essential partners through the recruitment and assembly of homo- and hetero-oligomers in order to strengthen the inflammatory response. The purpose of this review is to highlight the importance of some particular features of this multiligand receptor, its signaling cascade as well as the cross-talk with some members of the Toll-like receptor family.

Figure optionsDownload high-quality image (272 K)Download as PowerPoint slideHighlights
► RAGE is involved in both, physiological and physiopathological contexts.
► It works as a pattern-recognition receptor and cooperate with Toll-like receptors.
► RAGE engagement activates a complex downstream signaling network.
► Structural features, emerging ligands and signaling cascade are reviewed.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cellular Signalling - Volume 25, Issue 3, March 2013, Pages 609–614
نویسندگان
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