Development of Luciferase Reporter Gene-based Cell Bioassay for the Aromatic Hydrocarbon Receptor Agonists.
- Author:
Sun Young KIM
1
;
Eun Jung CHOI
;
Jae Ho YANG
Author Information
1. Department of Pharmacology, School of Medicine, Catholic University of Daegu, Daegu, Korea. yangjh@cu.ac.kr
- Publication Type:Original Article
- Keywords:
AhR agonist;
TCDD;
Bioassay;
Reporter gene;
Screening
- MeSH:
Animals;
Biological Assay*;
Carcinoma, Hepatocellular;
Cell Line;
Dioxins;
Drug Discovery;
Fireflies;
Genes, Reporter;
Luciferases*;
Mass Screening;
Mice;
Phenol;
Phenolsulfonphthalein;
Plasmids;
Prodrugs;
Tetrachlorodibenzodioxin;
Transcription Factors;
Transfection
- From:The Korean Journal of Physiology and Pharmacology
2006;10(6):349-354
- CountryRepublic of Korea
- Language:English
-
Abstract:
The aromatic hydrocarbon receptor (AhR) is a ligand-activated transcription factor that mediates many of the biological and toxicological effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, dioxin) and related chemicals. The application of recombinant reporter plasmid such as the firefly luciferase gene has proven to be a very effective method to detect these chemicals. The bioassay system, CALUX, is sensitive in directly detecting AhR-agonists from a variety of environmental and biologic materials. However, responses of the AhR-dependent bioassays are dependent on the cell types used. Thus, we developed a sensitive bioassay using the recombinant mouse hepatoma cell (Hepa1c1c7) for the determination of dioxins. The recombinant cell line was stably transfected with firefly luciferase reporter gene (pGudLuc1.1). The transfected cells showed the highest induction of luciferase activity at 4.5 hr and a decrease beyond this time point. The system showed the highest sensitivity of detection ever reported. Upon TCDD exposure cells showed 2 fold increase at 10 pM and 7 fold increase at 100 pM, respectively. The passage number after the transfection played an important role in the sensitivity. The increase of passage number tended to increase the sensitivity of the cells up to 15. The media without phenol red showed a higher induction rate than with phenol red, suggesting the preferable use of phenol red-free media for the bioassay. Since each of the assays has unique characteristics that make them suitable for some screening applications and not others, development of sensitive bioanalytical methods based on a variety of cellular systems in a key to the successful determination of dioxins. The bioassay system developed in this study will contribute to further development of successful screening the AhR agonists among the environmental mixture. In addition, the rapid and sensitive nature of this cellular system can be applied as a valuable tool to screen the dioxin-like moieties among the prodrugs at the initial stage, thereby expediting the new drug discovery.
