Lauf P K, Joiner C H
Blood. 1976 Sep;48(3):457-68.
Potassium (K+) influx and 3H-ouabain binding were studied in human red cells completely lacking the rhesus (Rh) antigens (Rhnull cells) and compared with normal Rh(D) red cells. The Rhnull cells, originally described by Seidl, Spielmann, and Martin (Vox Sang. 23:182, 1972) were normal in size, cation, and water content, indicating no significant increase in cell volume as occurs in young human red cells. However, the ouabain-insensitive K+ permeability, as well as the ouabain sensitive active K+ transport, were increased 1.6 1.8-and 1.4-1.5-fold, respectively, above the values found in Rh(D) control cells. The Na+K+ ATPase activity of membranes from Rhnull cells was also higher than from Rh(D) cells. Binding studies with 3H-ouabain revealed that at 100% K+ pump inhibition Rhnull cells bound 670 and Rh(D) cells 450-500 ouabain molecules per cell. Since the rate of ouabain binding was identical in Rhnull and Rh(D) control cells, we concluded that the Rhnull cell had about 35%-45% more cation pumps than the Rh(D) cell. These additional pumps in Rhnull cells appeared to be indistinguishable from those in control cells. Anti-D or the serum from the Rhnull individual did not alter cation permeability in Rh(D) red cells. The data suggested that the Rhnull cell, known for its hematologic malfunction, was not a young or prematurely released red cell, but had a pleiotropic membrane defect which also affected the passive and active cation transport system on the molecular level. Our finding precludes a structural identity of the rhesus antigen with the molecules composing the Na+K+ pump system.
对完全缺乏恒河猴(Rh)抗原的人红细胞(Rhnull细胞)的钾离子(K+)内流和3H-哇巴因结合进行了研究,并与正常Rh(D)红细胞进行了比较。最初由Seidl、Spielmann和Martin描述的Rhnull细胞(《血液学杂志》23:182,1972)在大小、阳离子和水分含量方面均正常,这表明其细胞体积没有像年轻人类红细胞那样显著增加。然而,哇巴因不敏感的K+通透性以及哇巴因敏感的活性K+转运分别比Rh(D)对照细胞中的值增加了1.6至1.8倍和1.4至1.5倍。Rhnull细胞膜的Na+K+ATP酶活性也高于Rh(D)细胞。用3H-哇巴因进行的结合研究表明,在100%K+泵抑制时,每个Rhnull细胞结合670个哇巴因分子,而Rh(D)细胞结合450至500个。由于在Rhnull细胞和Rh(D)对照细胞中哇巴因的结合速率相同,我们得出结论,Rhnull细胞的阳离子泵比Rh(D)细胞多约35%至45%。Rhnull细胞中的这些额外泵似乎与对照细胞中的泵没有区别。抗-D或Rhnull个体的血清不会改变Rh(D)红细胞中的阳离子通透性。数据表明,以血液学功能异常而闻名的Rhnull细胞不是年轻或过早释放的红细胞,而是具有多效性膜缺陷,这也在分子水平上影响了被动和主动阳离子转运系统。我们的发现排除了恒河猴抗原与构成Na+K+泵系统的分子在结构上的一致性。