Examination of Glucocorticoid receptor alpha-mediated transcriptional regulation of P-glycoprotein, CYP3A4, and CYP2C9 genes in placental trophoblast cell lines
Language English Country Netherlands Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
17572486
DOI
10.1016/j.placenta.2007.05.001
PII: S0143-4004(07)00112-9
Knihovny.cz E-resources
- MeSH
- Transcriptional Activation physiology MeSH
- Aryl Hydrocarbon Hydroxylases biosynthesis MeSH
- Cell Line MeSH
- Cytochrome P-450 CYP3A MeSH
- Cytochrome P-450 CYP2C9 MeSH
- Dexamethasone pharmacology MeSH
- Hepatocyte Nuclear Factor 4 physiology MeSH
- Humans MeSH
- RNA, Messenger metabolism MeSH
- Cell Line, Tumor MeSH
- ATP Binding Cassette Transporter, Subfamily B, Member 1 biosynthesis MeSH
- Promoter Regions, Genetic physiology MeSH
- Receptors, Glucocorticoid physiology MeSH
- Cytochrome P-450 Enzyme System biosynthesis MeSH
- Pregnancy MeSH
- Trophoblasts metabolism MeSH
- Check Tag
- Humans MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Aryl Hydrocarbon Hydroxylases MeSH
- CYP2C9 protein, human MeSH Browser
- CYP3A4 protein, human MeSH Browser
- Cytochrome P-450 CYP3A MeSH
- Cytochrome P-450 CYP2C9 MeSH
- Dexamethasone MeSH
- glucocorticoid receptor alpha MeSH Browser
- Hepatocyte Nuclear Factor 4 MeSH
- HNF4A protein, human MeSH Browser
- RNA, Messenger MeSH
- ATP Binding Cassette Transporter, Subfamily B, Member 1 MeSH
- Receptors, Glucocorticoid MeSH
- Cytochrome P-450 Enzyme System MeSH
The placental trophoblast at different stages of pregnancy contains some drug transporters and xenobiotic-metabolising enzymes, as well as ligand-activated nuclear receptors, which control their inducible transcriptional regulation. Glucocorticoid receptor alpha (GRalpha) is expressed in both placental syncytiotrophoblast and cytotrophoblast. GRalpha was shown to control inducible expression of several enzymes of the cytochrome P-450 family (CYP) and the drug transporter P-glycoprotein in the liver. However, GRalpha-mediated transcriptional regulation of drug transporters and CYPs has not been studied in the placental trophoblast. In this study, we examined the expression and activity of GRalpha in the transcriptional regulation of P-glycoprotein, CYP3A4, and CYP2C9 in placental trophoblast cell lines. Employing RT-PCR, Western blotting, and luciferase gene reporter assay, we detected the expression and activity of GRalpha in JEG3 and BeWo cell lines. However, we observed that only MDR1 mRNA was up-regulated after treatment of placental cells with dexamethasone. Accordingly, only the promoter of the MDR1 gene was activated by dexamethasone in gene reporter assays in placental cells and the activation was abolished by RU486, an antagonist of GRalpha. CYP3A4 and CYP2C9 promoters were activated in placental cells only after co-transfection with hepatocyte nuclear factor 4alpha (HNF4alpha), which indicates the hepatocyte-specific character of GRalpha-mediated regulation of the genes. On the other hand, coexpression of HNF4alpha had no effect on the activation of the MDR1 gene promoter, suggesting HNF4alpha-independent regulation via GRalpha. We conclude that GRalpha may be involved in the transcriptional regulation of P-glycoprotein in the placental trophoblast. We also indicate that the CYP3A4 and CYP2C9 genes are not inducible through GRalpha in placental cell lines, due to the lack of HNF4alpha expression and possibly some additional hepatocyte-specific transcriptional factors.
References provided by Crossref.org
Metformin suppresses pregnane X receptor (PXR)-regulated transactivation of CYP3A4 gene