Schenerman M A, Leister K J, Trachtenberg D K, Racker E
Section of Biochemistry, Molecular, and Cell Biology, Cornell University, Ithaca, New York 14853.
J Cell Physiol. 1988 May;135(2):157-62. doi: 10.1002/jcp.1041350202.
Mouse embryo fibroblast cells (C3H-10T1/2) and the methylcholanthrene-transformed derivative (MCA-10T1/2) were treated with basal modified Eagle's medium (BME) containing 10% fetal bovine serum and varying concentrations of ouabain ranging from 0.05 mM to 0.7 mM for 16 h in culture. After replacing the ouabain-containing medium with Earl's balanced salts solution, System A amino acid transport activity increased from approximately 40 to 500 pmol AIB accumulated.mg protein-1.min-1 in the C3H-10T1/2 cells and from approximately 300 to 700 pmol AIB accumulated.mg protein-1.min-1 in the MCA-10T1/2 cells. The (Na+/K+)-ATPase pump activity also increased from approximately 12 to 46 nmol Rb+ accumulated.mg protein-1.min-1 in the normal cells and from approximately 20 to 42 nmol Rb+ accumulated.mg protein-1.min-1 in the transformed cells. System A and the (Na+/K+)ATPase activity were maximally increased at approximately 0.4-0.6 mM ouabain in the normal cells in contrast to the transformed cells which were maximally stimulated at a concentration of approximately 0.2 mM ouabain. This treatment with ouabain increased the [Na+]i/[K+]i as measured by atomic absorption spectroscopy, and thereby decreased the Na+ and K+ electrochemical gradients. Our data show that the internal ion gradients inverted at a lower concentration of ouabain in the transformed cells compared to the normal cells. The ouabain-induced increase in pump and System A activity shown here was used as a tool to further investigate the coordinated ion transport regulation in the control of cell growth.
将小鼠胚胎成纤维细胞(C3H - 10T1/2)和经甲基胆蒽转化的衍生物(MCA - 10T1/2)在含有10%胎牛血清且哇巴因浓度在0.05 mM至0.7 mM之间变化的基础改良 Eagle 培养基(BME)中培养16小时。在用厄尔平衡盐溶液替换含哇巴因的培养基后,A系统氨基酸转运活性在C3H - 10T1/2细胞中从约40 pmol AIB积累·mg蛋白-1·min-1增加到500 pmol AIB积累·mg蛋白-1·min-1,在MCA - 10T1/2细胞中从约300 pmol AIB积累·mg蛋白-1·min-1增加到700 pmol AIB积累·mg蛋白-1·min-1。正常细胞中(Na+/K+)-ATP酶泵活性也从约12 nmol Rb+积累·mg蛋白-1·min-1增加到46 nmol Rb+积累·mg蛋白-1·min-1,转化细胞中从约20 nmol Rb+积累·mg蛋白-1·min-1增加到42 nmol Rb+积累·mg蛋白-1·min-1。与转化细胞在约0.