Emanuel J R, Garetz S, Schneider J, Ash J F, Benz E J, Levenson R
Mol Cell Biol. 1986 Jul;6(7):2476-81. doi: 10.1128/mcb.6.7.2476-2481.1986.
We have studied the mechanism of cellular resistance to cardiac glycosides in C+ cells. C+ cells were resistant to ouabain and overproduced plasma membrane-bound Na,K-ATPase relative to parental HeLa cells. Overexpression of Na,K-ATPase in C+ cells correlated with increased ATPase mRNA levels and amplification (approximately 100 times) of the ATPase gene. Growth of C+ cells in ouabain-free medium resulted in a marked decline in ATPase mRNA and DNA levels. However, when cells were reexposed to ouabain, they proliferated and ATPase mRNA and DNA sequences were reamplified. Restriction analysis of C+ and other human DNA samples revealed the occurrence of rearrangements in the region of the Na,K-ATPase gene in C+ cells. Furthermore, C+ cells expressed an ATPase mRNA species not found in HeLa cells. These results suggest that amplification of the gene coding for Na,K-ATPase results in overproduction of Na,K-ATPase polypeptides. Amplification of the ATPase gene or the expression of new ATPase mRNA sequences or both may also be responsible for acquisition of the ouabain-resistant phenotype.
我们研究了C+细胞对强心苷产生细胞抗性的机制。相对于亲代HeLa细胞,C+细胞对哇巴因具有抗性,并且过量产生与质膜结合的钠钾ATP酶。C+细胞中钠钾ATP酶的过表达与ATP酶mRNA水平的增加以及ATP酶基因的扩增(约100倍)相关。在不含哇巴因的培养基中培养C+细胞会导致ATP酶mRNA和DNA水平显著下降。然而,当细胞重新暴露于哇巴因时,它们会增殖,并且ATP酶mRNA和DNA序列会重新扩增。对C+细胞和其他人类DNA样本的限制性分析表明,C+细胞中钠钾ATP酶基因区域发生了重排。此外,C+细胞表达了一种HeLa细胞中未发现的ATP酶mRNA种类。这些结果表明,编码钠钾ATP酶的基因扩增导致钠钾ATP酶多肽的过量产生。ATP酶基因的扩增、新的ATP酶mRNA序列的表达或两者都可能是获得哇巴因抗性表型的原因。