Atherosclerosis: integration of its pathogenesis as a self-perpetuating propagating inflammation: a review

被引:45
作者
Poston, Robin N. [1 ]
机构
[1] Queen Mary Univ London, Ctr Microvasc Res, William Harvey Res Inst, Barts & London Sch Med & Dent, Charterhouse Sq, London EC1M 6BQ, England
关键词
adhesion molecule; atherosclerosis; dynamics; endothelium; inflammation; inflammatory mediator; low density lipoprotein; macrophage; oxidation; atherosclerotic plaque; positive feedback; LOW-DENSITY-LIPOPROTEIN; INTERCELLULAR-ADHESION MOLECULE-1; TUMOR-NECROSIS-FACTOR; ENDOTHELIUM-DEPENDENT VASODILATION; SMOOTH-MUSCLE CELLS; NF-KAPPA-B; CORONARY-ARTERY; OXIDIZED LDL; COMPLEMENT ACTIVATION; SCAVENGER RECEPTOR;
D O I
10.1097/XCE.0000000000000172
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This review proposes that the development of the atherosclerotic plaque is critically dependent on its inflammatory components forming a self-perpetuating and propagating positive feedback loop. The components involved are: (1) LDL oxidation, (2) activation of the endothelium, (3) recruitment of inflammatory monocytes, (4) macrophage accumulation, which induces LDL oxidation, and (5) macrophage generation of inflammatory mediators, which also activate the endothelium. Through these stages, the positive feedback loop is formed, which generates and promotes expansion of the atherosclerotic process. To illustrate this dynamic of lesion development, the author previously produced a computer simulation, which allowed realistic modelling. This hypothesis on atherogenesis can explain the existence and characteristic focal morphology of the atherosclerotic plaque. Each of the components contributing to the feedback loop is discussed. Many of these components also contain subsidiary positive feedback loops, which could exacerbate the overall process. Copyright (c) 2019 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:51 / 61
页数:11
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