Barenholz Y, Yechiel E, Cohen R, Deckelbaum R J
Cell Biophys. 1981 Jun;3(2):115-26. doi: 10.1007/BF02788128.
Acanthocytic red blood cells in patients with abetalipoproteinemia have a decrease membrane fluidity that is associated with increased sphingomyelin/phosphatidylcholine (SM/PC) ratios. Here we describe studies designed to gain better insight into (i) the interrelationship between the composition of lipoprotein and red blood cell membrane in abetalipoproteinemia patients and normal controls; and (ii) how the differences in lipid composition of the red blood cell membrane affect its fluidity. The increased SM/PC ratio found in abetalipoproteinemia plasma high density lipoproteins (HDL) (3 times greater than controls) was paralleled by an increase in this ratio in acanthocytic red cells, but to a lesser degree (almost twice greater than control red cells). Cholesterol/phospholipid mole ratios (C/P) were increased 3-fold in abetalipoproteinemia HDL, but only slightly increased in red cells compared to controls values. As in the controls, 80-85% of abetalipoproteinemia red cell sphingomyelin was found to be in the outer half of the erythrocyte membrane. Membrane fluidity was defined in terms of microviscosity (eta) between 5 and 42 degrees C by the fluorescent polarization of 1,6-diphenylhexatriene (DPH) present in erythrocyte ghost membranes. At all temperatures, membrane microviscosity was higher in abetalipoproteinemia ghosts than controls, but these differences decreased at higher temperatures (12.34 vs 9.79 poise, respectively at 10 degrees C; 4.63 vs 4.04 poise at 37 degrees C). These differences were eliminated after oxidation of all membrane cholesterol to cholest-4-en-3-one by incubation with cholesterol oxidase. Following cholesterol oxidation, the membrane microviscosity decreased in patient ghosts more than in normal red blood cells so that at all temperatures no significant differences were present relative to control ghosts, in which the apparent microviscosity was also diminished but to a lesser degree. Therefore, although increased SM/PC ratios in abetalipoproteinemia may be responsible for decreased erythrocyte membrane fluidity, these effects are dependent upon normal interactions of cholesterol with red cell phospholipid.
无β脂蛋白血症患者的棘红细胞膜流动性降低,这与鞘磷脂/磷脂酰胆碱(SM/PC)比值升高有关。在此,我们描述了旨在更深入了解以下两个方面的研究:(i)无β脂蛋白血症患者与正常对照者脂蛋白组成与红细胞膜组成之间的相互关系;(ii)红细胞膜脂质组成差异如何影响其流动性。无β脂蛋白血症患者血浆高密度脂蛋白(HDL)中发现的SM/PC比值升高(比对照者高3倍),棘红细胞中该比值也升高,但程度较小(几乎比对照红细胞高两倍)。胆固醇/磷脂摩尔比(C/P)在无β脂蛋白血症HDL中增加了3倍,但与对照值相比,红细胞中仅略有增加。与对照者一样,发现无β脂蛋白血症红细胞鞘磷脂的80 - 85%位于红细胞膜的外半部分。通过红细胞血影膜中存在的1,6 - 二苯基己三烯(DPH)的荧光偏振,在5至42℃之间以微粘度(η)定义膜流动性。在所有温度下,无β脂蛋白血症血影膜的膜微粘度均高于对照者,但这些差异在较高温度下减小(分别在10℃时为12.34与9.79泊;在37℃时为4.63与4.04泊)。通过与胆固醇氧化酶孵育将所有膜胆固醇氧化为胆甾 - 4 - 烯 - 3 - 酮后,这些差异消失。胆固醇氧化后,患者血影膜的膜微粘度降低幅度大于正常红细胞,因此在所有温度下与对照血影膜相比均无显著差异,对照血影膜的表观微粘度也降低,但程度较小。因此,尽管无β脂蛋白血症中SM/PC比值升高可能导致红细胞膜流动性降低,但这些效应取决于胆固醇与红细胞磷脂的正常相互作用。