Emory Lipid Research Laboratory, Emory University School of Medicine, 1670 Clairmont Road, Atlanta Veterans Affairs Medical Center, Mail Code 151 Room 4A187, Decatur, GA 30033, USA.
J Clin Lipidol. 2007 Mar;1(1):20-30. doi: 10.1016/j.jacl.2007.01.005. Epub 2007 Feb 15.
Several lines of evidence are available to support the protective effects of high-density lipoproteins (HDL) on atherosclerosis. The exact mechanisms by which HDL protects against atherosclerotic disease development are not understood. In addition to its role in the reverse transport of cholesterol from the peripheral sites to the liver for excretion, HDL also carries a number of enzymes that contribute to the remodeling of plasma lipoproteins and to the protection of other lipoproteins against oxidative modification. Many of these enzymes can play a role in determining the composition of circulating HDL, while others appear to affect specific biologic activities associated with HDL. It is not clear whether the concentrations of HDL particles or the activities associated with this class of particles are more important. One of the problems is that HDL constitutes a heterogeneous population of particles, and analytical tools to characterize the various subpopulations are not widely available. In this article, we will review the enzymes that are associated with plasma HDL and possible mechanisms as to how these may contribute to the protective properties of HDL in humans.
有几条证据支持高密度脂蛋白(HDL)对动脉粥样硬化的保护作用。目前还不了解 HDL 防止动脉粥样硬化发展的确切机制。除了在胆固醇从外周部位逆转运到肝脏排泄中的作用外,HDL 还携带许多酶,这些酶有助于重塑血浆脂蛋白,并保护其他脂蛋白免受氧化修饰。其中许多酶可以在决定循环 HDL 的组成中发挥作用,而其他酶似乎影响与 HDL 相关的特定生物学活性。目前还不清楚是 HDL 颗粒的浓度还是与该颗粒类相关的活性更为重要。其中一个问题是 HDL 是颗粒的不均匀群体,用于描述各种亚群的分析工具并不广泛。在本文中,我们将回顾与血浆 HDL 相关的酶以及这些酶可能如何有助于 HDL 在人类中的保护作用的可能机制。