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Role of Hepatic Lipase and Endothelial Lipase in High-Density Lipoprotein—Mediated Reverse Cholesterol Transport

机译:肝脂肪酶和内皮脂肪酶在高密度脂蛋白介导的胆固醇逆向转运中的作用

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摘要

Reverse cholesterol transport (RCT) constitutes a key part of the atheroprotective properties of high-density lipoproteins (HDL). Hepatic lipase (HL) and endothelial lipase (EL) are negative regulators of plasma HDL cholesterol levels. Although overexpression of EL decreases overall macrophage-to-feces RCT, knockout of both HL and EL leaves RCT essentially unaffected. With respect to important individual steps of RCT, current data on the role of EL and HL in cholesterol efflux are not conclusive. Both enzymes increase hepatic selective cholesterol uptake; however, this does not translate into altered biliary cholesterol secretion, which is regarded the final step of RCT. Also, the impact of HL and EL on atherosclerosis is not clear cut; rather it depends on respective experimental conditions and chosen models. More mechanistic insights into the diverse biological properties of these enzymes are therefore required to firmly establish EL and HL as targets for the treatment of atherosclerotic cardiovascular disease.
机译:胆固醇逆向转运(RCT)构成高密度脂蛋白(HDL)的抗动脉粥样硬化特性的关键部分。肝脂肪酶(HL)和内皮脂肪酶(EL)是血浆HDL胆固醇水平的负调节剂。尽管EL的过表达降低了从巨噬细胞到粪便的总体RCT,但HL和EL的敲除均未影响RCT。关于RCT的重要单个步骤,关于EL和HL在胆固醇外流中作用的最新数据尚无定论。两种酶均会增加肝脏对胆固醇的选择性吸收。然而,这不会转化为胆汁胆固醇分泌的改变,这被认为是RCT的最后一步。此外,HL和EL对动脉粥样硬化的影响尚不清楚。而是取决于各自的实验条件和所选模型。因此,需要对这些酶的多种生物学特性有更多的机械见解,才能将EL和HL牢固地确立为治疗动脉粥样硬化性心血管疾病的靶标。

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