Seigneuret M, Devaux P F
Proc Natl Acad Sci U S A. 1984 Jun;81(12):3751-5. doi: 10.1073/pnas.81.12.3751.
Spin-labeled analogs of phosphatidylcholine, phosphatidylserine, and phosphatidylethanolamine have been used to study phospholipid transverse diffusion and asymmetry in the human erythrocyte membrane. Ascorbate reduction was used to assess the transbilayer distribution of the labels. All three spin-labeled phospholipids initially incorporated into the outer leaflet of the membrane. On fresh erythrocytes at 5 degrees C, the phosphatidylcholine label remained mainly in the outer leaflet. In contrast, the phosphatidylserine and phosphatidylethanolamine labels underwent rapid transverse diffusion that led to their asymmetric distribution in favor of the inner leaflet. The latter effect was reversibly inhibited after ATP depletion of the erythrocytes and could be reproduced on resealed erythrocyte ghosts only if hydrolyzable Mg-ATP was included in the internal medium. It is suggested that an ATP-driven transport of amino phospholipids toward the inner leaflet could be the major cause of the phospholipid asymmetry in the erythrocyte membrane. It is also proposed that the same mechanism could explain the ATP requirement of the maintenance of the erythrocyte membrane discoid shape.
磷脂酰胆碱、磷脂酰丝氨酸和磷脂酰乙醇胺的自旋标记类似物已被用于研究人红细胞膜中磷脂的横向扩散和不对称性。使用抗坏血酸盐还原法来评估标记物的跨膜分布。所有三种自旋标记的磷脂最初都掺入到膜的外层。在5摄氏度的新鲜红细胞上,磷脂酰胆碱标记物主要保留在外层。相比之下,磷脂酰丝氨酸和磷脂酰乙醇胺标记物经历了快速的横向扩散,导致它们在内层的不对称分布。红细胞ATP耗竭后,后一种效应被可逆性抑制,并且只有在内介质中包含可水解的Mg-ATP时,才能在重新封闭的红细胞空壳上重现。有人提出,ATP驱动的氨基磷脂向内层的转运可能是人红细胞膜中磷脂不对称性的主要原因。还提出相同的机制可以解释维持红细胞膜盘状形状对ATP的需求。