Chu F F, Esworthy R S, Akman S, Doroshow J H
Department of Medical Oncology and Therapeutics Research, City of Hope National Medical Center, Duarte, CA 91010.
Nucleic Acids Res. 1990 Mar 25;18(6):1531-9. doi: 10.1093/nar/18.6.1531.
We have studied the effect of selenium on the expression of a cellular glutathione peroxidase, GSHPx-1, in transfected MCF-7 cells and in doxorubicin-resistant (Adrr) MCF-7 cells. A GSHPx-1 cDNA with a Rous Sarcoma virus promoter was transfected into a human mammary carcinoma cell line, MCF-7, which has very low endogenous cytosolic glutathione (GSH) peroxidase activity and no detectable message. The transfectant with the highest GSH peroxidase activity among the isolates, MCF-7H6, was characterized. Adrr MCF-7 cells, a subline of MCF-7 cells, also has elevated GSH peroxidase activity. GSH peroxidase expressed by MCF-7H6 and Adrr MCF-7 cells is similar to the endogenous GSHPx-1 based on molecular weight, immunoreactivity, and metabolic labeling with 75Se. MCF-7H6 and Adrr MCF-7 cells grown in Se-deficient media had 2.6 +/- 2.4 (mean +/- S.D.) and 4.2 +/- 3.6 units/mg protein of GSH peroxidase specific activity, respectively. Se supplementation increased GSH peroxidase activity in a concentration- and time-dependent fashion. Enzymatic activity reached a level of 164 +/- 62 in MCF-7H6 cells and 114 +/- 27 in Adrr MCF-7 cells within 5 days of growth in media supplemented with 30 nM Se. Northern analysis revealed that Se-deficient MCF-7H6 cells expressed 2.1 +/- 0.4-fold less GSHPx-1 mRNA than their Se-sufficient counterparts. Similarly, Se-deficient Adrr MCF-7 cells expressed 3.3 +/- 1.8-fold less GSHPx-1 mRNA than their Se-supplemented counterparts after the quantity of mRNA was normalized with beta-actin. These studies suggest that modulation of GSH peroxidase activity by Se in both MCF-7H6 transfectants expressing pRSV-GSHPx-1 and Adrr MCF-7 cells expressing endogenous GSHPx-1 occurs largely at the translational level, and to a lesser degree at the level of mRNA, possibly by stabilizing GSHPx-1 mRNA since the transfected cDNA in MCF-7H6 cells has only 5 nucleotides 5' to the AUG initiation codon.
我们研究了硒对转染的MCF-7细胞及多柔比星耐药(Adrr)MCF-7细胞中一种细胞谷胱甘肽过氧化物酶GSHPx-1表达的影响。将带有劳斯肉瘤病毒启动子的GSHPx-1 cDNA转染到人乳腺癌细胞系MCF-7中,该细胞系内源性胞质谷胱甘肽(GSH)过氧化物酶活性非常低且无可检测到的信息。对分离株中谷胱甘肽过氧化物酶活性最高的转染子MCF-7H6进行了特性分析。MCF-7细胞的亚系Adrr MCF-7细胞,其谷胱甘肽过氧化物酶活性也有所升高。基于分子量、免疫反应性以及用75Se进行的代谢标记,MCF-7H6和Adrr MCF-7细胞所表达的谷胱甘肽过氧化物酶与内源性GSHPx-1相似。在缺硒培养基中生长的MCF-7H6和Adrr MCF-7细胞,其谷胱甘肽过氧化物酶的比活性分别为2.6±2.4(平均值±标准差)和4.2±3.6单位/毫克蛋白。补充硒以浓度和时间依赖性方式增加了谷胱甘肽过氧化物酶活性。在补充了30 nM硒的培养基中生长5天后,MCF-7H6细胞的酶活性达到164±62,Adrr MCF-7细胞的酶活性达到114±27。Northern分析显示,缺硒的MCF-7H6细胞所表达的GSHPx-1 mRNA比硒充足的对应细胞少2.1±0.4倍。同样,在用β-肌动蛋白对mRNA量进行标准化后,缺硒的Adrr MCF-7细胞所表达的GSHPx-1 mRNA比补充硒的对应细胞少3.3±1.8倍。这些研究表明,在表达pRSV-GSHPx-1的MCF-7H6转染子和表达内源性GSHPx-1的Adrr MCF-7细胞中,硒对谷胱甘肽过氧化物酶活性的调节主要发生在翻译水平,在mRNA水平的调节程度较小,这可能是由于稳定了GSHPx-1 mRNA,因为MCF-7H6细胞中转染的cDNA在AUG起始密码子的5'端只有5个核苷酸。