Schwartz R S, Chiu D T, Lubin B
Curr Top Hematol. 1985;5:63-112.
By weight, phospholipids make up approximately 25% of the plasma membrane of mature human erythrocytes. The four major phospholipid species present in the membrane (PC, PE, PS, and SM) are distributed asymmetrically across the bilayer leaflet resulting in an enrichment of choline-phospholipid (PC and SM) in the outer leaflet and of amino-phospholipid (PE and PS) in the cytoplasmic leaflet. This asymmetric organization is preferentially maintained through complex, and at present, poorly understood noncovalent interactions between specific membrane lipids and proteins (in particular, a stabilizing role for the skeletal protein spectrin and band 4.1 have been implicated), although other considerations such as phospholipid net charge, size, and degree of acyl chain unsaturation may also be involved. In certain red cell pathologies, or following experimental manipulation, there is a partial loss of this asymmetry (summarized in Tables XVI, XVII) often resulting in increases in the outer leaflet content of amino-phospholipids and subsequent expression of altered membrane surface properties. Some of these abnormal properties may have pathophysiologic consequence; indeed, red cell membranes displaying increased levels of surface amino-phospholipids have been shown to be potent procoagulants and demonstrate enhanced intermembrane interactions with both model (liposomes) and biologic (mononuclear phagocytes) membranes. Redistribution of membrane phospholipids may not occur homogeneously throughout an entire leaflet but may be restricted to specific membrane regions. These studies strongly suggest that the maintenance of phospholipid asymmetry in human red cell membranes is not a trivial event but probably represents a homeostatic mechanism, the failure of which may lead to alterations in normal erythrocyte functions, and ultimately, survival.
按重量计算,磷脂约占成熟人类红细胞质膜的25%。膜中存在的四种主要磷脂种类(磷脂酰胆碱、磷脂酰乙醇胺、磷脂酰丝氨酸和鞘磷脂)在双层小叶中不对称分布,导致胆碱磷脂(磷脂酰胆碱和鞘磷脂)在外小叶富集,氨基磷脂(磷脂酰乙醇胺和磷脂酰丝氨酸)在细胞质小叶富集。这种不对称组织通过特定膜脂与蛋白质之间复杂且目前了解甚少的非共价相互作用优先维持(特别是,已表明骨架蛋白血影蛋白和带4.1具有稳定作用),尽管其他因素如磷脂净电荷、大小和酰基链不饱和度也可能参与其中。在某些红细胞病变或实验操作后,这种不对称性会部分丧失(总结于表十六、十七),常常导致氨基磷脂在外小叶的含量增加,随后膜表面性质发生改变。其中一些异常性质可能具有病理生理后果;事实上,已表明表面氨基磷脂水平升高的红细胞膜是强效促凝剂,并显示出与模型(脂质体)和生物(单核吞噬细胞)膜之间增强的膜间相互作用。膜磷脂的重新分布可能并非在整个小叶中均匀发生,而是可能局限于特定的膜区域。这些研究强烈表明,人类红细胞膜中磷脂不对称性的维持并非微不足道,而是可能代表一种稳态机制,其失效可能导致正常红细胞功能改变,最终影响生存。