人细胞色素P450 2E1在中国仓鼠V79细胞中的稳定表达

Wolfgang A. Schmalix , Martina Barrenscheen , Robert Landsiedel , Christine Janzowski , Gerhard Eisenbrand , Frank Gonzalez , Erik Eliasson , Magnus Ingelman-Sundberg , Monika Perchermeier , Helmut Greim , Johannes Doehmer
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引用次数: 43

摘要

通过将SV40早期启动子重组CYP2E1 cDNA整合到染色体DNA中,构建了稳定表达人细胞色素P450 2E1 (CYP2E1)的中国仓鼠V79细胞系。通过氯唑唑酮和对硝基苯酚的羟基化,CYP2E1编码的cDNA有效表达并具有酶活性,总蛋白× min - 1的速率约为70 pmol × mg - 1。在乙醇的存在下,CYP2E1的含量和活性增加,表明底物介导的稳定效应。对于CYP2E1抑制剂,如咪唑、4-甲基吡唑和异烟肼,也观察到类似的稳定作用。通过cyp2e1介导的n -亚硝基二甲胺和对硝基苯酚的激活以及剂量依赖性的细胞毒性和致突变作用,证明了新建立的细胞系V79MZh2E1进行毒理学研究的可行性。
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Stable expression of human cytochrome P450 2E1 in V79 Chinese hamster cells

A V79 Chinese hamster cell line was constructed for stable expression of human cytochrome P450 2E1 (CYP2E1) by integration of a SV40 Early promoter recombinant CYP2E1 cDNA into the chromosomal DNA. The cDNA encoded CYP2E1 was effectively expressed and enzymatically active, as shown by hydroxylation of chlorzoxazone and of p-nitrophenol, at rates of about 70 pmol × mg−1 total protein × min−1. CYP2E1 content and activity was increased upon cultivation in the presence of ethanol indicating a substrate mediated stabilization effect. A similar stabilizing effect was also observed for inhibitors of CYP2E1, e.g. imidazole, 4-methylpyrazole, and isoniazid. The feasibility of the newly established cell line V79MZh2E1 for toxicological studies was shown by CYP2E1-mediated activation of N-nitrosodimethylamine and p-nitrophenol and a dose-dependent cytotoxic and mutagenic effect.

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