Liu Sibo, Bi Hongfeng, Jiang Meiling, Chen Yuanli, Jiang Meixiu
The QUEEN MARY school, Nanchang University, 999 Xuefu Road, Nanchang, Jiangxi 330031, China.
Medical Equipment Department, Dongying Shengli Oilfield Central Hospital, Dongying, Shandong 257034, China.
Biomed Pharmacother. 2023 Apr;160:114321. doi: 10.1016/j.biopha.2023.114321. Epub 2023 Feb 1.
Atherosclerosis (AS) is a chronic inflammatory disease of large and medium arteries that includes lipid metabolism disorder and recruitment of immune cells to the artery wall. An increasing number of studies have confirmed that inflammasome over-activation is associated with the onset and progression of atherosclerosis. The NLRP3 inflammasome, in particular, has been proven to increase the incidence rate of cardiovascular diseases (CVD) by promoting pro-inflammatory cytokine release and reducing plaque stability. The strict control of inflammasome and prevention of excessive inflammatory reactions have been the research focus of inflammatory diseases. Tripartite motif (TRIM) is a protein family with a conservative structure and rapid evolution. Several studies have demonstrated the TRIM family's regulatory role in mediating inflammation. This review aims to clarify the relationship between TRIMs and NLRP3 inflammasome and provide insights for future research and treatment discovery.
动脉粥样硬化(AS)是一种发生于大中型动脉的慢性炎症性疾病,包括脂质代谢紊乱以及免疫细胞向动脉壁募集。越来越多的研究证实,炎性小体过度激活与动脉粥样硬化的发生和发展相关。尤其是NLRP3炎性小体,已被证明可通过促进促炎细胞因子释放和降低斑块稳定性来增加心血管疾病(CVD)的发病率。严格控制炎性小体并预防过度炎症反应一直是炎症性疾病的研究重点。三联基序(TRIM)是一个结构保守且进化迅速的蛋白质家族。多项研究已证明TRIM家族在介导炎症过程中的调节作用。本综述旨在阐明TRIMs与NLRP3炎性小体之间的关系,并为未来的研究和治疗发现提供思路。