吡喃结构域
炎症体
受体
炎症
缺血
细胞内
再灌注损伤
模式识别受体
细胞生物学
医学
生物
内科学
免疫学
先天免疫系统
心脏病学
作者
Zhiliang Guo,Shuhong Yu,Xin Chen,Ruidong Ye,Wusheng Zhu,Xinfeng Liu
出处
期刊:Cns & Neurological Disorders-drug Targets
[Bentham Science Publishers]
日期:2016-03-25
卷期号:15 (6): 699-712
被引量:92
标识
DOI:10.2174/1871527315666160321111829
摘要
Inflammation plays a pivotal role in the ischemia/reperfusion (I/R) injury. Inflammatory response is initiated by the detection of pathogen-associated molecular patterns and/or damage-associated molecular patterns via extracellular and intracellular pattern recognition receptors. The nucleotide-binding oligomerization domain–like receptor family, pyrin domain containing protein 3 (NLRP3) is a component of pattern recognition receptors and serves a vital role in inflammatory response by forming an intracellular multi-protein complex known as NLRP3 inflammasome. There is increasing evidence that NLRP3 inflammasome acts as guardians against host-derived danger materials. The inappropriate activation of NLRP3 contributes to the progression of I/R injury such as myocardial, cerebral, renal, hepatic and retinal I/R injuries. In this review, we summarize the role of NLRP3 in inflammatory response and discuss the relationship between NLRP3 and I/R injury. We also provide insights into new treatment strategies for targeting NLRP3 inflammasome, as well as the upstream and downstream components of NLRP3 in alleviating I/R injury. Keywords: Inflammasome, ischemia/reperfusion injury, NLRP3, treatment, targets.
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