AstraZeneca R&D Mölndal, Innovative Medicines, CVGI DMPK, S-431 83 Mölndal, Sweden.
Drug Metab Dispos. 2012 Nov;40(11):2054-8. doi: 10.1124/dmd.112.045815. Epub 2012 Jul 30.
The hepatic SV40 large T-antigen immortalized human liver epithelial (THLE) cell line and sublines transfected with cytochromes P450 (P450s) are increasingly being used for evaluation of potential drug-induced liver injury. So far, the available information on transporter and enzyme expression in these transfected cell systems is scattered. The purpose of this study was to characterize THLE cell lines with respect to transporter and enzyme expression. The mRNA expression of 96 typical drug absorption, distribution, metabolism and excretion genes, which encode a selection of transporters, phase I and II drug-metabolizing enzymes, and nuclear hormone receptors, was investigated in five THLE cell lines transfected with individual human P450s and in mock-transfected THLE-null cells using real-time polymerase chain reaction. The majority of the analyzed genes was either absent or expressed at low levels in the THLE-null and THLE-P450 cells, apart from housekeeping genes and the individual transfected P450s. Enzyme activity measurements provided confirmatory functional data for CYP2C9 and CYP3A4. Comparison with gene expression in human liver revealed an overall much lower gene expression in the THLE cell lines. The low levels of expression of a broad range of P450 genes in the THLE cell lines highlight the value of studies undertaken with P450-expressing cell lines for investigation of mechanisms of P450 metabolite-mediated hepatotoxicity. However, when attempting to translate between data obtained in THLE cell lines in vitro and functional consequences in vivo, it is important to take account of their limited expression of genes encoding many other drug-metabolizing enzymes and hepatic transporters.
SV40 大 T 抗原永生化人肝上皮(THLE)细胞系及其转染细胞色素 P450(P450s)的亚系越来越多地被用于评估潜在的药物性肝损伤。到目前为止,这些转染细胞系统中转运体和酶表达的可用信息是分散的。本研究的目的是表征 THLE 细胞系的转运体和酶表达。使用实时聚合酶链反应,研究了 5 种转染了个体人 P450 的 THLE 细胞系和转染了 THLE 空载体的 THLE-细胞系中 96 种典型药物吸收、分布、代谢和排泄基因的 mRNA 表达,这些基因编码了一系列转运体、I 相和 II 相药物代谢酶和核激素受体。除了管家基因和个体转染的 P450 外,THLE-空载体和 THLE-P450 细胞中大多数分析的基因要么不存在,要么表达水平很低。酶活性测量为 CYP2C9 和 CYP3A4 提供了确证的功能数据。与人类肝脏中的基因表达进行比较,THLE 细胞系中的总体基因表达水平要低得多。THLE 细胞系中广泛的 P450 基因表达水平低,突出了使用表达 P450 的细胞系进行 P450 代谢物介导的肝毒性机制研究的价值。然而,当试图在 THLE 细胞系体外获得的数据与体内功能后果之间进行翻译时,重要的是要考虑到它们编码许多其他药物代谢酶和肝转运体的基因表达有限。