Lipid trafficking in cardiovascular disease

被引:10
作者
Sposito, Andrei C. [1 ]
Zimetti, Francesca [2 ]
Barreto, Joaquim [1 ]
Zanotti, Ilaria [2 ]
机构
[1] State Univ Campinas Unicamp, Atherosclerosis & Vasc Biol Lab Aterolab, Sao Paulo, Brazil
[2] Univ Parma, Dept Food & Drug, Parma, Italy
来源
ADVANCES IN CLINICAL CHEMISTRY, VOL 92 | 2019年 / 92卷
关键词
LOW-DENSITY-LIPOPROTEIN; PHOSPHOLIPID TRANSFER PROTEIN; ESTER TRANSFER PROTEIN; HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; TRIGLYCERIDE TRANSFER PROTEIN; ACID LIPASE DEFICIENCY; SCAVENGER RECEPTOR BI; CORONARY-ARTERY-DISEASE; FLUID-PHASE PINOCYTOSIS; FOAM CELL-FORMATION;
D O I
10.1016/bs.acc.2019.04.002
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The reduction of plasma apolipoprotein B (apoB) containing lipoproteins has long been pursued as the main modifiable risk factor for the development of cardiovascular disease (CVD). This has led to an intense search for strategies aiming at reducing plasma apoB-lipoproteins, culminating in reduction of overall CV risk. Despite 3 decades of progress, CVD remains the leading cause of morbidity and mortality worldwide and, as such, new therapeutic targets are still warranted. Clinical and preclinical research has moved forward from the original concept, under which some lipids must be accumulated and other removed to achieve the ideal condition in disease prevention, into the concept that mechanisms that orchestrate lipid movement between lipoproteins, cells and organelles is equally involved in CVD. As such, this review scrutinizes potentially atherogenic changes in lipid trafficking and assesses the molecular mechanisms behind it. New developments in risk assessment and new targets for the mitigation of residual CVD risk are also addressed.
引用
收藏
页码:105 / 140
页数:36
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