Cameron I L, Cox L A, Liu X R, Fullerton G D
Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio 78284.
J Cell Physiol. 1991 Dec;149(3):365-74. doi: 10.1002/jcp.1041490303.
Is an intact plasma membrane responsible for keeping hemoglobin and water within the human erythrocyte? If not, what is responsible? How free is Hb to move about within the erythrocyte? To answer these questions erythrocytes were taken for phase contrast microscopy, transmission electron microscopy (TEM), determination of water-holding capacity, and proton NMR studies both before and after membrane disruption with a nonionic detergent (Brij 58). Addition of 0.2% Brij to a D2O saline solution of hemoglobin (Hb) caused particles of Hb to appear and to aggregate. This aggregation of Hb caused the amplitude of the Hb proton NMR spectra to decrease. Thus, the less mobile the Hb the lower the Hb proton spectra amplitude. Erythrocytes washed in D2O saline showed proton NMR spectra of relatively low amplitude. Addition of Brij (0.2%) to these erythrocytes caused increased Hb mobility within these erythrocytes. The TEM of fixed and thin-sectioned erythrocytes treated with Brij showed disruption of the plasma membrane of all erythrocytes regardless of whether or not they had lost Hb. Brij-permeabilized erythrocytes washed in D2O saline or in a D2O K buffer maintained a higher heavy water-holding capacity upon centrifugation as compared to nonpermeabilized erythrocytes. The TEM of Brij-treated and washed erythrocyte "shells" revealed a continuous submembrane lamina but no other evidence of cytoskeletal elements. The water-holding capacity of the erythrocyte can be accounted for by the water-holding capacity of hemoglobin. The evidence favors a relatively immobile state of Hb and of water in the erythrocyte that is not immediately dependent on an intact plasma membrane but is attributed to interactions between Hb molecules and the submembrane lamina.
完整的质膜是否负责将血红蛋白和水保留在人体红细胞内?如果不是,那是什么在起作用?血红蛋白(Hb)在红细胞内的移动自由度如何?为了回答这些问题,在用非离子去污剂(Brij 58)破坏膜之前和之后,对红细胞进行了相差显微镜检查、透射电子显微镜(TEM)检查、持水量测定和质子核磁共振研究。向血红蛋白(Hb)的重水溶液中添加0.2%的Brij会导致Hb颗粒出现并聚集。这种Hb聚集导致Hb质子核磁共振谱的振幅降低。因此,Hb的流动性越低,Hb质子谱的振幅就越低。在重水溶液中洗涤的红细胞显示出相对较低振幅的质子核磁共振谱。向这些红细胞中添加Brij(0.2%)会使这些红细胞内的Hb流动性增加。用Brij处理的固定和薄切片红细胞的TEM显示,所有红细胞的质膜均被破坏,无论它们是否失去了Hb。与未通透的红细胞相比,用Brij通透的红细胞在重水溶液或重水钾缓冲液中洗涤后,离心时保持较高的重水持水量。用Brij处理并洗涤后的红细胞“壳”的TEM显示有连续的膜下薄片,但没有细胞骨架成分的其他证据。红细胞的持水量可以由血红蛋白的持水量来解释。证据支持红细胞内Hb和水处于相对固定的状态,这并非直接依赖于完整的质膜,而是归因于Hb分子与膜下薄片之间的相互作用。