Schulz J T, Cantley L C
Department of Physiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
J Biol Chem. 1988 Jan 15;263(2):624-32.
The cation-transporting activity and Na,K-ATPase activity of CV-1 cell recipients of the mouse ouabain resistance gene (ouaR6, or OR6 cells; see Levenson, R., Racaniello, V., Albritton, L., and Housman, D. (1984) Proc. Natl. Acad. Sci. U. S. A. 81, 1489-1493) have been further characterized. OR6 cells grown in strophanthidin (a cardiac aglycon which may be removed rapidly from the Na,K-ATPase) possess both ouabain-sensitive and -insensitive 86Rb+ uptake activities. The ouabain-sensitive 86Rb+ uptake activity of these cells (OR6-S cells) exhibits the same Ki for ouabain as that of the CV-1 parent cells (Ki(app) = 3 x 10(-7) M ouabain), but accounts for only approximately 30% of total 86Rb+ uptake into Na+-loaded OR6-S cells, compared to 80% for CV-1 cells. Most of the ouabain-resistant 86Rb+ uptake in OR6-S cells is dependent on internal Na+ and is insensitive to furosemide, suggesting that it is due to an ouabain-resistant Na,K pump. In OR6-S cell lysates, 50% of Na+-dependent ATPase activity is insensitive to 1 mM ouabain, compared to less than 5% in CV-1 cell lysates. In addition, purified plasma membranes from OR6-S cells contain a 100-kDa protein which is transiently phosphorylated by ATP in an Na+-dependent, K+-sensitive manner, like the alpha subunit of the CV-1 Na,K-ATPase and the canine renal Na,K-ATPase, but which is unaffected by preincubation in 1 mM ouabain. All of these data suggest that OR6-S cells possess a ouabain-insensitive Na,K pump with characteristics similar to the ouabain-sensitive pump of CV-1 parent cells. Since the mouse ouabain resistance gene does not encode either subunit of the Na,K-ATPase, these results suggest that the ouabain resistance gene product may modify the ouabain sensitivity of the endogenous CV-1 Na,K pump.
已对小鼠哇巴因抗性基因(ouaR6,即OR6细胞;见列文森,R.,拉卡涅洛,V.,阿尔布里顿,L.,和豪斯曼,D.(1984年)《美国国家科学院院刊》81,1489 - 1493)的CV - 1细胞受体的阳离子转运活性和钠钾ATP酶活性进行了进一步表征。在毒毛旋花子苷(一种可迅速从钠钾ATP酶上移除的强心苷配基)中生长的OR6细胞同时具有对哇巴因敏感和不敏感的⁸⁶Rb⁺摄取活性。这些细胞(OR6 - S细胞)对哇巴因敏感的⁸⁶Rb⁺摄取活性对哇巴因的Ki与CV - 1亲本细胞相同(Ki(app)=3×10⁻⁷ M哇巴因),但在钠负载的OR6 - S细胞中,其仅占总⁸⁶Rb⁺摄取量的约30%,而CV - 1细胞为80%。OR6 - S细胞中大部分对哇巴因抗性的⁸⁶Rb⁺摄取依赖于细胞内钠离子且对速尿不敏感,这表明它是由一种对哇巴因抗性的钠钾泵引起的。在OR6 - S细胞裂解物中,50%的依赖钠离子的ATP酶活性对1 mM哇巴因不敏感,而CV - 1细胞裂解物中这一比例小于5%。此外,从OR6 - S细胞纯化的质膜含有一种100 kDa的蛋白质,它能以依赖钠离子、对钾离子敏感的方式被ATP短暂磷酸化,类似于CV - 1钠钾ATP酶的α亚基和犬肾钠钾ATP酶,但在1 mM哇巴因中预孵育后不受影响。所有这些数据表明,OR6 - S细胞拥有一种对哇巴因不敏感的钠钾泵,其特性与CV - 1亲本细胞对哇巴因敏感的泵相似。由于小鼠哇巴因抗性基因不编码钠钾ATP酶的任何一个亚基,这些结果表明哇巴因抗性基因产物可能会改变内源性CV - 1钠钾泵对哇巴因的敏感性。