首页> 美国卫生研究院文献>Nucleic Acids Research >Modulation of glutathione peroxidase expression by selenium: effect on human MCF-7 breast cancer cell transfectants expressing a cellular glutathione peroxidase cDNA and doxorubicin-resistant MCF-7 cells.
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Modulation of glutathione peroxidase expression by selenium: effect on human MCF-7 breast cancer cell transfectants expressing a cellular glutathione peroxidase cDNA and doxorubicin-resistant MCF-7 cells.

机译:硒对谷胱甘肽过氧化物酶表达的调节:对表达细胞谷胱甘肽过氧化物酶cDNA和抗阿霉素的MCF-7细胞的人MCF-7乳腺癌细胞转染子的影响。

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摘要

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.
机译:我们已经研究了硒对转染的MCF-7细胞和抗阿霉素(Adrr)MCF-7细胞中细胞谷胱甘肽过氧化物酶GSHPx-1表达的影响。将带有Rous肉瘤病毒启动子的GSHPx-1 cDNA转染至人乳腺癌细胞系MCF-7,该细胞系具有极低的内源性胞质谷胱甘肽(GSH)过氧化物酶活性,并且未检测到任何信息。分离株中具有最高GSH过氧化物酶活性的转染子MCF-7H6进行了表征。 Adrr MCF-7细胞是MCF-7细胞的亚系,其GSH过氧化物酶活性也升高。 MCF-7H6和Adrr MCF-7细胞表达的GSH过氧化物酶在分子量,免疫反应性和75Se代谢标记方面与内源性GSHPx-1相似。在缺硒培养基中生长的MCF-7H6和Adrr MCF-7细胞分别具有2.6 +/- 2.4(平均+/- S.D.)和4.2 +/- 3.6单位/毫克的GSH过氧化物酶比活性蛋白。硒的补充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30 nM Se的培养基中生长5天之内,MCF-7H6细胞的酶促活性达到164 +/- 62,Adrr MCF-7细胞的酶促活性达到114 +/- 27。 Northern分析表明,硒缺乏的MCF-7H6细胞表达的GSHPx-1 mRNA比硒缺乏的MCF-7H6少2.1 +/- 0.4倍。类似地,在用β-肌动蛋白对mRNA的量进行标准化后,Se缺失的Adrr MCF-7细胞表达的GSHPx-1 mRNA比其Se补充的对应细胞少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,Se对GSH过氧化物酶活性的调节主要发生在翻译水平,而在水平上则较低。 mRNA,可能是通过稳定GSHPx-1 mRNA来实现的,因为MCF-7H6细胞中转染的cDNA的AUG起始密码子只有5'个核苷酸。

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