標題: Sterol Regulatory Element Binding Protein 2 Activation of NLRP3 Inflammasome in Endothelium Mediates Hemodynamic-Induced Atherosclerosis Susceptibility
作者: Xiao, Han
Lu, Min
Lin, Ting Yang
Chen, Zhen
Chen, Gang
Wang, Wei-Chi
Marin, Traci
Shentu, Tzu-pin
Wen, Liang
Gongol, Brendan
Sun, Wei
Liang, Xiao
Chen, Ju
Huang, Hsien-Da
Pedra, Joao H. F.
Johnson, David A.
Shyy, John Y-J.
生物資訊及系統生物研究所
Institude of Bioinformatics and Systems Biology
關鍵字: atherosclerosis;endothelial cell;NLRP3 protein;human;shear stress;sterol regulatory element binding proteins
公開日期: 6-八月-2013
摘要: Background-The molecular basis for the focal nature of atherosclerotic lesions is poorly understood. Here, we explored whether disturbed flow patterns activate an innate immune response to form the NLRP3 inflammasome scaffold in vascular endothelial cells via sterol regulatory element binding protein 2 (SREBP2). Methods and Results-Oscillatory flow activates SREBP2 and induces NLRP3 inflammasome in endothelial cells. The underlying mechanisms involve SREBP2 transactivating NADPH oxidase 2 and NLRP3. Consistently, SREBP2, NADPH oxidase 2, and NLRP3 levels were elevated in atheroprone areas of mouse aortas, suggesting that the SREBP2-activated NLRP3 inflammasome causes functionally disturbed endothelium with increased inflammation. Mimicking the effect of atheroprone flow, endothelial cell-specific overexpression of the activated form of SREBP2 synergized with hyperlipidemia to increase atherosclerosis in the atheroresistant areas of mouse aortas. Conclusions-Atheroprone flow induces NLRP3 inflammasome in endothelium through SREBP2 activation. This increased innate immunity in endothelium synergizes with hyperlipidemia to cause topographical distribution of atherosclerotic lesions.
URI: http://dx.doi.org/10.1161/CIRCULATIONAHA.113.002714
http://hdl.handle.net/11536/22567
ISSN: 0009-7322
DOI: 10.1161/CIRCULATIONAHA.113.002714
期刊: CIRCULATION
Volume: 128
Issue: 6
起始頁: 632
結束頁: 642
顯示於類別:期刊論文


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