STABLE EXPRESSION OF HUMAN CYTOCHROME-P450 2E1 IN V79 CHINESE-HAMSTER CELLS

被引:29
|
作者
SCHMALIX, WA
BARRENSCHEEN, M
LANDSIEDEL, R
JANZOWSKI, C
EISENBRAND, G
GONZALEZ, F
ELIASSON, E
INGELMANSUNDBERG, M
PERCHERMEIER, M
GREIM, H
DOEHMER, J
机构
[1] TECH UNIV MUNICH,INST TOXIKOL & UMWELTHYG,D-80636 MUNICH,GERMANY
[2] UNIV KAISERSLAUTERN,D-67663 KAISERSLAUTERN,GERMANY
[3] NCI,MOLEC CARCINOGENESIS LAB,BETHESDA,MD 20892
[4] KAROLINSKA INST,DEPT MED BIOCHEM & BIOPHYS,S-17177 STOCKHOLM,SWEDEN
[5] GSF,FORSCHUNGSZENTRUM UMWELT & GESUNDHEIT,INST TOXIKOL,D-85758 OBERSCHLEISSHEIM,GERMANY
关键词
CYTOCHROME P450; CYTOCHROME P450 2E1; V79 CHINESE HAMSTER CELL; P-NITROPHENOL; CHLORZOXAZONE; N-NITROSODIMETHYLAMINE;
D O I
10.1016/S0014-2999(05)80004-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 x mg(-1) total protein X 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.
引用
收藏
页码:123 / 131
页数:9
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