TOLL-LIKE RECEPTORS IN ISCHEMIA-REPERFUSION INJURY

被引:308
作者
Arumugam, Thiruma V. [1 ]
Okun, Eitan [2 ]
Tang, Sung-Chun [3 ]
Thundyil, John [1 ]
Taylor, Stephen M. [4 ]
Woodruff, Trent M. [4 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Pharmaceut Sci, Sch Pharm, Amarillo, TX 79106 USA
[2] NIA, Neurosci Lab, Intramural Res Program, Baltimore, MD 21224 USA
[3] Natl Taiwan Univ Hosp, Dept Neurol, Yunlin, Taiwan
[4] Univ Queensland, Sch Biomed Sci, Brisbane, Qld, Australia
来源
SHOCK | 2009年 / 32卷 / 01期
关键词
Toll-like receptors; ischemia-reperfusion injury; myocardial infarction; neuron; stroke; apoptosis; NF-KAPPA-B; MEDIATES ISCHEMIA/REPERFUSION INJURY; NECROSIS-FACTOR-ALPHA; IN-VIVO EXPRESSION; OXIDATIVE STRESS; INFLAMMATORY RESPONSE; DENDRITIC CELLS; INNATE IMMUNITY; UP-REGULATION; LUNG INJURY;
D O I
10.1097/SHK.0b013e318193e333
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Ischemia-reperfusion (I/R) injuries are implicated in a large array of pathological conditions such as myocardial infarction, cerebral stroke, and hepatic, renal, and intestinal ischemia, as well as following cardiovascular and transplant surgeries. The hallmark of these pathologies is excessive inflammation. Toll-like receptors (TLRs) are recognized as one of the main contributors to pathogen-induced inflammation and, more recently, injury-induced inflammation. Endogenous ligands such as low-molecular hyaluronic acid, fibronectin, heat shock protein 70, and heparin sulfate were all found to be cleaved in the inflamed tissue and to activate TLR2 and TLR4, initiating an inflammatory response even in the absence of pathogens and infiltrating immune cells. In this review, we discuss the contribution of TLR activation in hepatic, renal, cerebral, intestinal, and myocardial I/R injuries. A greater understanding of the role of TLRs in I/R injuries may aid in the development of specific TLR-targeted therapeutics to treat these conditions.
引用
收藏
页码:4 / 16
页数:13
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