Loeb J, Dawson G
Mol Cell Biochem. 1983;52(2):161-76. doi: 10.1007/BF00224925.
The term human serum high density lipoprotein (HDL) represents a range of lipid-protein complexes which are identified by their density and hence their relative lipid-protein content. Because HDL composition is variable, any proposed mechanisms for lipid and protein exchange must account for this variability. More importantly, since HDL has been repeatedly shown to be a negative risk factor in atherosclerosis, physical interactions have to be put in a physiological context. In this review, the lipid and protein exchange reactions of HDL with other lipoproteins, phospholipid vesicles, lipid-coated glass beads and isolated cells, will be considered. Particular emphasis will be placed on the role of the two major apoproteins of HDL, namely apo A-I and apo A-II, in these exchange reactions and a model will be presented to explain how these apoproteins might mediate lipid exchange, interconversions of lipoprotein particles, and the egress and excretion of lipid from cells.
术语“人血清高密度脂蛋白(HDL)”代表了一系列脂质 - 蛋白质复合物,它们通过密度以及相对的脂质 - 蛋白质含量来识别。由于HDL的组成是可变的,任何提出的脂质和蛋白质交换机制都必须考虑到这种变异性。更重要的是,由于HDL已被反复证明是动脉粥样硬化的负性危险因素,因此必须将物理相互作用置于生理背景中。在本综述中,将考虑HDL与其他脂蛋白、磷脂囊泡、脂质包被的玻璃珠和分离细胞之间的脂质和蛋白质交换反应。将特别强调HDL的两种主要载脂蛋白,即载脂蛋白A-I和载脂蛋白A-II在这些交换反应中的作用,并将提出一个模型来解释这些载脂蛋白如何介导脂质交换、脂蛋白颗粒的相互转化以及脂质从细胞中的流出和排泄。