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Review
. 2012 Oct;38(10):1588-98.
doi: 10.1007/s00134-012-2624-y. Epub 2012 Jul 10.

The receptor for advanced glycation end products and acute lung injury/acute respiratory distress syndrome

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Review

The receptor for advanced glycation end products and acute lung injury/acute respiratory distress syndrome

Weidun Alan Guo et al. Intensive Care Med. 2012 Oct.

Abstract

The receptor for advanced glycation end products (RAGE) is a pattern-recognition receptor and evolutionary member of the immunoglobulin superfamily that is involved in the host response to infection, injury, and inflammation. It exists in two forms: membrane-bound and soluble forms (sRAGE). RAGE recognizes a variety of ligands and, via a receptor-driven signaling cascade, activates the transcription factor NF-κB, leading to the expression of proinflammatory cytokines. The soluble form, sRAGE, is a decoy receptor and competitively inhibits membrane RAGE activation. RAGE is constitutively expressed abundantly in the lung under basal conditions. This expression is enhanced during inflammatory states such as with acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). This review summarizes the characteristics of RAGE, RAGE isoforms, RAGE ligands, and signaling pathways in the pathogenesis of ALI and ARDS. Additionally, the review explores the potential of RAGE as an important therapeutic target in ALI/ARDS.

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References

    1. Genes Cells. 2004 Feb;9(2):165-74 - PubMed
    1. Blood. 2010 Aug 5;116(5):841-9 - PubMed
    1. Cell Tissue Res. 2006 Mar;323(3):475-88 - PubMed
    1. Nat Genet. 2010 Jan;42(1):36-44 - PubMed
    1. J Gerontol A Biol Sci Med Sci. 2009 Jun;64(6):629-35 - PubMed

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