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RAGE regulation and signaling in inflammation and beyond

Journal of Leukocyte Biology · 2013 · Vol. 94(1) · pp. 55–68
Katrin KierdorfG. Fritz

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.

Advanced Glycation End Products researchImmune Response and InflammationDiabetes and associated disordersRage (emotion)BiologyCell biologyProinflammatory cytokineInflammationReceptorSignal transductionCell adhesion moleculeInnate immune systemImmune system

MeSH terms

Receptor for Advanced Glycation End ProductsAnimalsHumansInflammationReceptors, ImmunologicSignal Transduction

Funding

  • Deutsche Forschungsgemeinschaft
Citations
419
FWCI
11.33
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178
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99%
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