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缺血再灌注损伤中的Toll样受体

Toll-like receptors in ischemia-reperfusion injury.

作者信息

Arumugam Thiruma V, Okun Eitan, Tang Sung-Chun, Thundyil John, Taylor Stephen M, Woodruff Trent M

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, Texas 79106, USA.

出版信息

Shock. 2009 Jul;32(1):4-16. doi: 10.1097/SHK.0b013e318193e333.

Abstract

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.

摘要

缺血再灌注(I/R)损伤与一系列病理状况有关,如心肌梗死、脑卒中和肝、肾及肠道缺血,以及心血管手术和移植手术后的情况。这些病理状况的标志是过度炎症反应。Toll样受体(TLRs)被认为是病原体诱导炎症以及最近损伤诱导炎症的主要促成因素之一。内源性配体,如低分子透明质酸、纤连蛋白、热休克蛋白70和硫酸肝素,均在炎症组织中被切割,并激活TLR2和TLR4,即使在没有病原体和浸润免疫细胞的情况下也能引发炎症反应。在本综述中,我们讨论了TLR激活在肝、肾、脑、肠和心肌I/R损伤中的作用。对TLRs在I/R损伤中的作用有更深入的了解,可能有助于开发针对TLR的特异性疗法来治疗这些疾病。

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