Shibuya M L, Miura T, Lillehaug J R, Farley R A, Landolph J R
Department of Pathology, University of Southern California, Los Angeles.
Mol Toxicol. 1989 Apr-Jun;2(2):75-98.
To further understand the molecular nature of changes leading to chemically induced ouabain resistance in C3H/10T1/2 Cl 8 (10T1/2) cells, we isolated plasma membranes from wild-type and ouabain-resistant (Ouar) 10T1/2 cells and characterized (Na,K)-ATPase activity in the plasma membrane fraction. (Na+,K+)-ATPase enzyme activity in membrane fractions extracted from wild-type 10T1/2 cells was inhibited in a concentration-dependent manner by ouabain and was completely inhibited by 2.4 mM ouabain. Lineweaver-Burke and Eisenthal/Cornish-Bowden analysis indicated that the inhibition was uncompetitive. Ten to 45% of (Na+,K+)-ATPase enzyme activity extracted from three Ouar 10T1/2 cell lines cultured in 1 mM ouabain was resistant to 2.4 mM ouabain, depending on the cell line. Resistance of (Na+,K+)-ATPase activity in the plasma membrane fraction of Ouar cells to inhibition by ouabain and resistance of cultured Ouar cells to the cytotoxicity of ouabain occurred over similar concentrations of ouabain (0.1-3mM). Two ouabain-resistant cell lines, Ouar MNNG Cl 2 and Ouar MCA Cl 16-7, demonstrated the same total (Na+,K+)-ATPase specific activity as 10T1/2 cells, but the fraction of Ouar enzyme activity increased (from 18 to 40% in MNNG Cl 2 cells and from 10 to 25% in Sp Ouar Cl 16 cells) when the cells were cultured in ouabain. Thermal denaturation profiles and pH dependence profiles of (Na+,K+)-ATPase activity in plasma membranes from wild-type and Ouar 10T1/2 cells were identical. A 3.9-kb (Na,K)-ATPase alpha subunit mRNA transcript was found in 10T1/2 cells, and in the Ouar MNNG Cl 2 cell line cultured in the presence or absence of ouabain. There was no amplification of the gene coding for the alpha subunit of (Na+,K+)-ATPase in the chemically induced Ouar MNNG Cl 2 cell line, whether this cell line was cultured in the presence or absence of ouabain. These studies provide further evidence that the Ouar phenotype of chemically induced and spontaneous Ouar 10T1/2 cell lines derives from Ouar (Na+,K+)-ATPase activity, and that this Ouar (Na+,K+)-ATPase activity increases further in some cell lines cultured in the presence of ouabain.
为了进一步了解导致C3H/10T1/2 Cl 8(10T1/2)细胞化学诱导哇巴因抗性变化的分子本质,我们从野生型和哇巴因抗性(Ouar)10T1/2细胞中分离出质膜,并对质膜组分中的(Na,K)-ATP酶活性进行了表征。从野生型10T1/2细胞中提取的膜组分中的(Na +,K +)-ATP酶活性受到哇巴因浓度依赖性抑制,并且在2.4 mM哇巴因时被完全抑制。Lineweaver-Burke和Eisenthal/Cornish-Bowden分析表明这种抑制是非竞争性的。从在1 mM哇巴因中培养的三种Ouar 10T1/2细胞系中提取的(Na +,K +)-ATP酶活性的10%至45%对2.4 mM哇巴因具有抗性,这取决于细胞系。Ouar细胞质膜组分中(Na +,K +)-ATP酶活性对哇巴因抑制的抗性以及培养的Ouar细胞对哇巴因细胞毒性的抗性在相似的哇巴因浓度(0.1 - 3 mM)下出现。两种哇巴因抗性细胞系,Ouar MNNG Cl 2和Ouar MCA Cl 16 - 7,表现出与10T1/2细胞相同的总(Na +,K +)-ATP酶比活性,但当细胞在哇巴因中培养时,Ouar酶活性的比例增加(MNNG Cl 2细胞中从18%增加到40%,Sp Ouar Cl 16细胞中从10%增加到25%)。野生型和Ouar 10T1/2细胞质膜中(Na +,K +)-ATP酶活性的热变性曲线和pH依赖性曲线是相同的。在10T1/2细胞以及在有无哇巴因存在下培养的Ouar MNNG Cl 2细胞系中发现了一个3.9 kb的(Na,K)-ATP酶α亚基mRNA转录本。在化学诱导的Ouar MNNG Cl 2细胞系中,无论该细胞系在有无哇巴因存在下培养,编码(Na +,K +)-ATP酶α亚基的基因均未扩增。这些研究提供了进一步的证据,表明化学诱导和自发的Ouar 10T1/2细胞系的Ouar表型源自Ouar(Na +,K +)-ATP酶活性,并且这种Ouar(Na +,K +)-ATP酶活性在一些在哇巴因存在下培养的细胞系中进一步增加。