RRC ID 4587
著者 Omasa T, Kim K, Hiramatsu S, Katakura Y, Kishimoto M, Enosawa S, Ohtake H.
タイトル Construction and evaluation of drug-metabolizing cell line for bioartificial liver support system.
ジャーナル Biotechnol Prog
Abstract Focusing on drug metabolism in liver, we constructed and evaluated a drug-metabolizing bioartificial liver (BAL) support system. In a previous study, we constructed ammonia-metabolizing CHO and hepatoma-derived HepG2 cell lines by recombination of the glutamine synthetase (GS) gene. For further mimicking of liver metabolism, the human hepatoma-derived cell line HepG2 was transformed by the pBudCE-GS-CYP3A4 vector, which contains GS and drug-metabolizing CYP 3A4 genes. The constructed GS-3A4-HepG2 cell line showed 3A4 activity higher than that of human primary hepatocytes. The drug-metabolizing activity of BAL (BAL clearance) was evaluated using this cell line. The estimated clearance was higher than that of the human hepatocyte system.
巻・号 21(1)
ページ 161-7
公開日 2005-1-1
DOI 10.1021/bp049757a
PMID 15903254
MeSH Ammonia / metabolism Animals Bioreactors CHO Cells Cell Culture Techniques / methods Cell Line, Tumor Cells, Cultured Cricetinae Cytochrome P-450 CYP3A Cytochrome P-450 Enzyme System / genetics Cytochrome P-450 Enzyme System / metabolism* Dimercaprol / metabolism* Dimercaprol / pharmacokinetics Glutamate-Ammonia Ligase / genetics Glutamate-Ammonia Ligase / metabolism* Humans Liver, Artificial* Metabolic Clearance Rate Recombinant Proteins / metabolism Transfection
IF 2.334
引用数 9
WOS 分野 FOOD SCIENCE & TECHNOLOGY BIOTECHNOLOGY & APPLIED MICROBIOLOGY
リソース情報
ヒト・動物細胞 CHO-K1(RCB0285) Hep G2(RCB0459) GS-HepG2(RCB1681)