Genetically engineered mammalian cells and applications

被引:7
作者
Doehmer, J [1 ]
Schneider, A [1 ]
Fassbender, M [1 ]
Soballa, V [1 ]
Schmalix, WA [1 ]
Greim, H [1 ]
机构
[1] GSF, FORSCHUNGSZENTRUM, INST TOXICOL, D-85758 OBERSCHLEISSHEIM, GERMANY
关键词
biotransformation; xenobiotics; cytochrome P450; heterologous expression;
D O I
10.1016/0378-4274(95)03523-0
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
In general, cells genetically engineered for stable and defined expression of xenobiotic-metabolizing enzymes are useful tools whenever a metabolism-related problem in toxicology and pharmacology is to be solved. It is the genetic and phenotypic nature of a given cell that determines its applicability. Mammalian cells have useful characteristics not given in bacterial, yeast or insect cells, which also may express xenobiotic-metabolizing enzymes. It is the problem to be solved and the question to be answered which determine the optimal choice for the best-suited expression system. There may even be subtle differences between mammalian cells of different species and organ origin, which might play a role in choosing a mammalian expression system. Thus, the level and specificity of the xenobiotic-metabolizing enzyme, the experimental testing conditions, and the biological endpoints present in a chosen cell are the most important criteria to be observed in the application of the mammalian expression systems.
引用
收藏
页码:823 / 827
页数:5
相关论文
共 10 条
[1]   STABLE EXPRESSION OF RAT CYTOCHROME P-450IIB1 CDNA IN CHINESE-HAMSTER CELLS (V79) AND METABOLIC-ACTIVATION OF AFLATOXIN-B1 [J].
DOEHMER, J ;
DOGRA, S ;
FRIEDBERG, T ;
MONIER, S ;
ADESNIK, M ;
GLATT, H ;
OESCH, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) :5769-5773
[2]  
DOEHMER J, 1991, METHOD ENZYMOL, V206, P117
[3]  
DOGRA S, 1990, MOL PHARMACOL, V37, P608
[4]   BIOTRANSFORMATION OF CAFFEINE AND THEOPHYLLINE IN MAMMALIAN-CELL LINES GENETICALLY ENGINEERED FOR EXPRESSION OF SINGLE CYTOCHROME-P450 ISOFORMS [J].
FUHR, U ;
DOEHMER, J ;
BATTULA, N ;
WOLFEL, C ;
KUDLA, C ;
KEITA, Y ;
STAIB, AH .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (02) :225-235
[5]   METABOLIC-ACTIVATION TO A MUTAGEN OF 3-HYDROXY-TRANS-7,8-DIHYDROXY-7,8-DIHYDROBENZO[A]PYRENE, A SECONDARY METABOLITE OF BENZO[A]PYRENE [J].
GLATT, H ;
SEIDEL, A ;
RIBEIRO, O ;
KIRKBY, C ;
HIROM, P ;
OESCH, F .
CARCINOGENESIS, 1987, 8 (11) :1621-1627
[6]  
GLATT HR, 1993, POLYCYCLIC AROMATI S, V3, P1167
[7]   THE P450 SUPERFAMILY - UPDATE ON NEW SEQUENCES, GENE-MAPPING, ACCESSION NUMBERS, EARLY TRIVIAL NAMES OF ENZYMES, AND NOMENCLATURE [J].
NELSON, DR ;
KAMATAKI, T ;
WAXMAN, DJ ;
GUENGERICH, FP ;
ESTABROOK, RW ;
FEYEREISEN, R ;
GONZALEZ, FJ ;
COON, MJ ;
GUNSALUS, IC ;
GOTOH, O ;
OKUDA, K ;
NEBERT, DW .
DNA AND CELL BIOLOGY, 1993, 12 (01) :1-51
[8]   STABLE EXPRESSION OF HUMAN CYTOCHROME-P450 1A1 CDNA IN V79 CHINESE-HAMSTER CELLS AND METABOLIC-ACTIVATION OF BENZO[A]PYRENE [J].
SCHMALIX, WA ;
MASER, H ;
KIEFER, F ;
REEN, R ;
WIEBEL, FJ ;
GONZALEZ, F ;
SEIDEL, A ;
GLATT, H ;
GREIM, H ;
DOEHMER, J .
EUROPEAN JOURNAL OF PHARMACOLOGY-ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY SECTION, 1993, 248 (03) :251-261
[9]  
SCHMALIX WA, 1995, IN PRESS EUR J PHARM
[10]   STABLE EXPRESSION OF RAT CYTOCHROME P450IA2 CDNA AND HYDROXYLATION OF 17-BETA-ESTRADIOL AND 2-AMINOFLUORENE IN V79 CHINESE-HAMSTER CELLS [J].
WOLFEL, C ;
PLATT, KL ;
DOGRA, S ;
GLATT, H ;
WACHTER, F ;
DOEHMER, J .
MOLECULAR CARCINOGENESIS, 1991, 4 (06) :489-498