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      The Pattern Recognition Receptor (RAGE) Is a Counterreceptor for Leukocyte Integrins : A Novel Pathway for Inflammatory Cell Recruitment

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          Abstract

          The pattern recognition receptor, RAGE (receptor for advanced glycation endproducts), propagates cellular dysfunction in several inflammatory disorders and diabetes. Here we show that RAGE functions as an endothelial adhesion receptor promoting leukocyte recruitment. In an animal model of thioglycollate-induced acute peritonitis, leukocyte recruitment was significantly impaired in RAGE-deficient mice as opposed to wild-type mice. In diabetic wild-type mice we observed enhanced leukocyte recruitment to the inflamed peritoneum as compared with nondiabetic wild-type mice; this phenomenon was attributed to RAGE as it was abrogated in the presence of soluble RAGE and was absent in diabetic RAGE-deficient mice. In vitro, RAGE-dependent leukocyte adhesion to endothelial cells was mediated by a direct interaction of RAGE with the β2-integrin Mac-1 and, to a lower extent, with p150,95 but not with LFA-1 or with β1-integrins. The RAGE–Mac-1 interaction was augmented by the proinflammatory RAGE-ligand, S100-protein. These results were corroborated by analysis of cells transfected with different heterodimeric β2-integrins, by using RAGE-transfected cells, and by using purified proteins. The RAGE–Mac-1 interaction defines a novel pathway of leukocyte recruitment relevant in inflammatory disorders associated with increased RAGE expression, such as in diabetes, and could provide the basis for the development of novel therapeutic applications.

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          Most cited references29

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

          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.
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            Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases.

            The receptor for advanced glycation end products (RAGE), a multi-ligand member of the immunoglobulin superfamily of cell surface molecules, interacts with distinct molecules implicated in homeostasis, development and inflammation, and certain diseases such as diabetes and Alzheimer's disease. Engagement of RAGE by a ligand triggers activation of key cell signalling pathways, such as p21ras, MAP kinases, NF-kappaB and cdc42/rac, thereby reprogramming cellular properties. RAGE is a central cell surface receptor for amphoterin, a polypeptide linked to outgrowth of cultured cortical neurons derived from developing brain. Indeed, the co-localization of RAGE and amphoterin at the leading edge of advancing neurites indicated their potential contribution to cellular migration, and in pathologies such as tumour invasion. Here we demonstrate that blockade of RAGE-amphoterin decreased growth and metastases of both implanted tumours and tumours developing spontaneously in susceptible mice. Inhibition of the RAGE-amphoterin interaction suppressed activation of p44/p42, p38 and SAP/JNK MAP kinases; molecular effector mechanisms importantly linked to tumour proliferation, invasion and expression of matrix metalloproteinases.
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              Ligand binding to integrins.

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                Author and article information

                Journal
                J Exp Med
                The Journal of Experimental Medicine
                The Rockefeller University Press
                0022-1007
                1540-9538
                17 November 2003
                : 198
                : 10
                : 1507-1515
                Affiliations
                [1 ]Department of Internal Medicine I, University Heidelberg, D-69115 Heidelberg, Germany
                [2 ]Institute for Medical Biometry and Informatics, University Heidelberg, D-69120 Heidelberg, Germany
                [3 ]Third Department of Internal Medicine, Justus-Liebig-University, D-35392 Giessen, Germany
                [4 ]Institute for Biochemistry, Justus-Liebig-University, D-35392 Giessen, Germany
                [5 ]Institute for Clinical Chemistry, Justus-Liebig-University, D-35392 Giessen, Germany
                [6 ]Department of Molecular Immunology, German Cancer Research Center, D-69120 Heidelberg, Germany
                [7 ]Berlex Biosciences, Richmond, CA 94806
                Author notes

                Address correspondence to Dr. T. Chavakis, Department of Internal Medicine I, University Heidelberg, Bergheimer Strasse 58, D-69115 Heidelberg, Germany. Phone: 49-6221-5638603; Fax: 49-6221-564101. email: triantafyllos.chavakis@ 123456med.uni-heidelberg.de

                Article
                20030800
                10.1084/jem.20030800
                2194124
                14623906
                06316927-01d8-4cbc-bcc4-df2b23845e69
                Copyright © 2003, The Rockefeller University Press
                History
                : 14 May 2003
                : 22 August 2003
                Categories
                Article

                Medicine
                integrin,adhesion,rage,diabetes,leukocyte
                Medicine
                integrin, adhesion, rage, diabetes, leukocyte

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