| Literature DB >> 27518621 |
Caitlin Lynch1, Jinghua Zhao1, Hongbing Wang2, Menghang Xia3.
Abstract
The constitutive androstane receptor (CAR, NR1I3) is responsible for the transcription of multiple drug metabolizing enzymes and transporters. There are two possible methods of activation for CAR, direct ligand binding and a ligand-independent method, which makes this a unique nuclear receptor. Both of these mechanisms require translocation of CAR from the cytoplasm into the nucleus. Interestingly, CAR is constitutively active in immortalized cell lines due to the basal nuclear location of this receptor. This creates an important challenge in most in vitro assay models because immortalized cells cannot be used without inhibiting the high basal activity. In this book chapter, we go into detail of how to perform quantitative high-throughput screens to identify hCAR1 modulators through the employment of a double stable cell line. Using this line, we are able to identify activators, as well as deactivators, of the challenging nuclear receptor, CAR.Entities:
Keywords: Constitutive Androstane Receptor (CAR); Cytochrome P450 2B6 (CYP2B6); Luciferase; Quantitative high-throughput screening (qHTS)
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Year: 2016 PMID: 27518621 PMCID: PMC5341601 DOI: 10.1007/978-1-4939-6346-1_4
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745