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培养时间对原代人肝细胞及肝癌细胞系HepG2中药物代谢酶表达的影响

Influence of culture time on the expression of drug-metabolizing enzymes in primary human hepatocytes and hepatoma cell line HepG2.

作者信息

Wilkening Stefan, Bader Augustinus

机构信息

German Research Centre for Biotechnology, Mascheroder Weg 1, 38124 Braunschweig, Germany.

出版信息

J Biochem Mol Toxicol. 2003;17(4):207-13. doi: 10.1002/jbt.10085.

Abstract

Primary cultures of human hepatocytes and hepatoma cell line HepG2 are frequently used to evaluate the hepatic disposition of drugs and other xenobiotics. To check the variability of the expression of drug-metabolizing enzymes in these in vitro models, expression of genes coding for several cytochrome P450 isoforms and phase II enzymes was quantified during culture time by real-time RT-PCR. Gene expression was determined daily for primary hepatocytes maintained in a sandwich culture over 1 week and for HepG2, during the first 10 passages. In primary hepatocytes characteristic expression trends were observed which could be abstracted into three major classes of time curves. Genes of the first and the second class had an expression maximum around day 6 and day 4 in culture, respectively. The third class of genes had two expression peaks: at day 1 and 5 in culture. Surprisingly, also the cell line HepG2 showed significant expression changes during passages. For example, gene expression of cytochrome 1A1 varied 8-fold, that of cytochrome 2B6 30-fold, and that of NADP-quinone reductase 1 more than 200-fold within the first 10 passages. In conclusion, neither primary hepatocytes nor HepG2 cell line display a model for constant expression of drug-metabolizing enzymes.

摘要

人肝细胞原代培养物和肝癌细胞系HepG2常用于评估药物及其他外源性物质的肝脏处置情况。为检测这些体外模型中药物代谢酶表达的变异性,通过实时逆转录聚合酶链反应(RT-PCR)在培养期间对编码几种细胞色素P450同工型和II相酶的基因表达进行定量。对于维持在夹心培养中的原代肝细胞,在1周内每天测定基因表达;对于HepG2细胞系,则在最初10代期间每天测定基因表达。在原代肝细胞中观察到了特征性的表达趋势,这些趋势可归纳为三大类时间曲线。第一类和第二类基因在培养的第6天和第4天左右分别有表达最大值。第三类基因有两个表达峰值:分别在培养的第1天和第5天。令人惊讶的是,细胞系HepG2在传代过程中也显示出显著的表达变化。例如,在最初10代内,细胞色素1A1的基因表达变化了8倍,细胞色素2B6的基因表达变化了30倍,NADP-醌还原酶1的基因表达变化超过200倍。总之,原代肝细胞和HepG2细胞系均未表现出药物代谢酶恒定表达的模型。

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