RAGE mediates a novel proinflammatory axis: A central cell surface receptor for S100/calgranulin polypeptides

被引:41
作者
Hofmann, MA
Drury, S
Fu, CF
Qu, W
Taguchi, A
Lu, Y
Avila, C
Kambham, N
Bierhaus, A
Nawroth, P
Neurath, MF
Slattery, T
Beach, D
McClary, J
Nagashima, M
Morser, J
Stern, D
Schmidt, AM
机构
[1] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
[2] Berlex Biosci, Richmond, CA 94804 USA
[3] Univ Tubingen, D-72076 Tubingen, Germany
[4] Univ Mainz, D-55101 Mainz, Germany
关键词
D O I
10.1016/S0092-8674(00)80801-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S100/calgranulin polypeptides are present at sites of inflammation, likely released by inflammatory cells targeted to such loci by a range of environmental cues. We report here that receptor for AGE (RAGE) is a central cell surface receptor for EN-RAGE (extracellular newly identified RAGE-binding protein) and related members of the S100/calgranulin superfamily. Interaction of EN-RAGEs with cellular RAGE on endothelium, mononuclear phagocytes, and lymphocytes triggers cellular activation, with generation of key proinflammatory mediators. Blockade of EN-RAGE/RAGE quenches delayed-type hypersensitivity and inflammatory colitis in murine models by arresting activation of central signaling pathways and expression of inflammatory gene mediators. These data highlight a novel paradigm in inflammation and identify roles for EN-RAGEs and RAGE in chronic cellular activation and tissue injury.
引用
收藏
页码:889 / 901
页数:13
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