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

被引:69
|
作者
Guo, Weidun Alan [1 ]
Knight, Paul R. [2 ]
Raghavendran, Krishnan [3 ]
机构
[1] SUNY Buffalo, Dept Surg, Buffalo, NY 14215 USA
[2] SUNY Buffalo, Dept Anesthesiol, Buffalo, NY 14215 USA
[3] Univ Michigan Hlth Syst, Dept Surg, Ann Arbor, MI USA
关键词
Receptor for advanced glycation end products; Acute lung injury; Acute respiratory distress syndrome; Damage-associated molecular patterns; ALVEOLAR FLUID CLEARANCE; CELL-SURFACE RECEPTOR; MOBILITY GROUP BOX-1; SOLUBLE RECEPTOR; MULTILIGAND RECEPTOR; EXPERIMENTAL-MODELS; SEVERE TRAUMA; EARLY RELEASE; I CELLS; RAGE;
D O I
10.1007/s00134-012-2624-y
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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-kappa B, 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.
引用
收藏
页码:1588 / 1598
页数:11
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