Novel Strategies in the Early Detection and Treatment of Endothelial Cell-Specific Mitochondrial Dysfunction in Coronary Artery Disease

被引:8
作者
Lee, Weiqian E. [1 ,2 ]
Genetzakis, Elijah [1 ,2 ]
Figtree, Gemma A. [1 ,2 ,3 ]
机构
[1] Univ Sydney, Kolling Inst, Sydney, NSW 2006, Australia
[2] Univ Sydney, Fac Med & Hlth, Sydney, NSW 2006, Australia
[3] Northern Sydney Local Hlth Dist, Royal North Shore Hosp, Dept Cardiol, Sydney, NSW 2065, Australia
基金
英国医学研究理事会;
关键词
coronary artery disease; endothelial dysfunction; mitochondrial dysfunction; endothelial colony forming cells; drug screening; atherosclerosis; SMuRFless; OXIDATIVE STRESS; APOLIPOPROTEIN-E; P2X7; RECEPTOR; ATHEROSCLEROTIC LESIONS; UNCOUPLING PROTEIN-2; CAPTIVE CHIMPANZEES; HYPOCHLOROUS ACID; P2X(7) RECEPTOR; HEART-FAILURE; OXIDIZED ATP;
D O I
10.3390/antiox12071359
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although elevated cholesterol and other recognised cardiovascular risk factors are important in the development of coronary artery disease (CAD) and heart attack, the susceptibility of humans to this fatal process is distinct from other animals. Mitochondrial dysfunction of cells in the arterial wall, particularly the endothelium, has been strongly implicated in the pathogenesis of CAD. In this manuscript, we review the established evidence and mechanisms in detail and explore the potential opportunities arising from analysing mitochondrial function in patient-derived cells such as endothelial colony-forming cells easily cultured from venous blood. We discuss how emerging technology and knowledge may allow us to measure mitochondrial dysfunction as a potential biomarker for diagnosis and risk management. We also discuss the "pros and cons" of animal models of atherosclerosis, and how patient-derived cell models may provide opportunities to develop novel therapies relevant for humans. Finally, we review several targets that potentially alleviate mitochondrial dysfunction working both via direct and indirect mechanisms and evaluate the effect of several classes of compounds in the cardiovascular context.
引用
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页数:27
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