Yui Y, Aoyama T, Morishita H, Takahashi M, Takatsu Y, Kawai C
Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
J Clin Invest. 1988 Sep;82(3):803-7. doi: 10.1172/JCI113682.
Serum PGI2 stabilizing factor (PSF) was purified from human serum to a single protein with a molecular weight of 28,000 D by SDS-PAGE. Analyses of NH2-terminal sequence (32 residues), COOH-terminal sequence (3 residues) and the composition of amino acids disclosed its homology with human apolipoprotein A-I (Apo A-I), a major apolipoprotein of HDL. Apolipoprotein A-II, C-I, C-II, C-III, D and E, as well as LDL, and VLDL did not possess this activity. The alpha-helix structure of Apo A-I is necessary for the binding of PGI2. HDL and nascent HDL reconstituted from Apo A-I and phospholipid significantly prolonged the half-life of PGI2. PGI2 stabilization by HDL and Apo A-I may be an important protective action against the accumulation of platelet thrombi at sites of vascular damage. The beneficial effect of HDL in the prevention of coronary artery disease may be partly due to this action.
血清前列环素稳定因子(PSF)通过SDS-PAGE从人血清中纯化至单一蛋白质,分子量为28,000 D。对其氨基末端序列(32个残基)、羧基末端序列(3个残基)和氨基酸组成的分析揭示了它与人载脂蛋白A-I(Apo A-I)的同源性,Apo A-I是高密度脂蛋白(HDL)的主要载脂蛋白。载脂蛋白A-II、C-I、C-II、C-III、D和E,以及低密度脂蛋白(LDL)和极低密度脂蛋白(VLDL)均不具备这种活性。Apo A-I的α-螺旋结构对于前列环素(PGI2)的结合是必需的。由Apo A-I和磷脂重构的HDL和新生HDL显著延长了PGI2的半衰期。HDL和Apo A-I对PGI2的稳定作用可能是针对血管损伤部位血小板血栓形成的一种重要保护作用。HDL在预防冠状动脉疾病方面的有益作用可能部分归因于这一作用。