-
Je něco špatně v tomto záznamu ?
Examination of glucocorticoid receptor alpha-mediated transcriptional regulation of P-glycoprotein, CYP3A4, and CYP2C9 genes in placental trophoblast cell lines
P. Pavek, L. Cerveny, L. Svecova, M. Brysch, A. Libra, R. Vrzal, P. Nachtigal, F. Staud, J. Ulrichova, Z. Fendrich, Z. Dvorak
Jazyk angličtina Země Velká Británie
Typ dokumentu srovnávací studie
- MeSH
- aktivace transkripce fyziologie MeSH
- aromatické hydroxylasy biosyntéza MeSH
- buněčné linie MeSH
- cytochrom P-450 CYP3A MeSH
- dexamethason farmakologie MeSH
- financování organizované MeSH
- hepatocytární jaderný faktor 4 fyziologie MeSH
- lidé MeSH
- messenger RNA metabolismus MeSH
- nádorové buněčné linie MeSH
- P-glykoprotein biosyntéza MeSH
- promotorové oblasti (genetika) fyziologie MeSH
- receptory glukokortikoidů fyziologie MeSH
- systém (enzymů) cytochromů P-450 biosyntéza MeSH
- těhotenství MeSH
- trofoblasty metabolismus MeSH
- Check Tag
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- srovnávací studie 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.
- 000
- 04062naa 2200517 a 4500
- 001
- bmc10013238
- 003
- CZ-PrNML
- 005
- 20120713143227.0
- 008
- 100602s2007 xxk e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Pávek, Petr $7 xx0093070
- 245 10
- $a Examination of glucocorticoid receptor alpha-mediated transcriptional regulation of P-glycoprotein, CYP3A4, and CYP2C9 genes in placental trophoblast cell lines / $c P. Pavek, L. Cerveny, L. Svecova, M. Brysch, A. Libra, R. Vrzal, P. Nachtigal, F. Staud, J. Ulrichova, Z. Fendrich, Z. Dvorak
- 314 __
- $a Department of Pharmacology and Toxicology, Faculty of Pharmacy, Charles University, Heyrovskoho 1203, Hradec Kralove 500 05, Czech Republic. petr.pavek@faf.cuni.cz
- 520 9_
- $a 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.
- 650 _2
- $a aromatické hydroxylasy $x biosyntéza $7 D001189
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a nádorové buněčné linie $7 D045744
- 650 _2
- $a cytochrom P-450 CYP3A $7 D051544
- 650 _2
- $a systém (enzymů) cytochromů P-450 $x biosyntéza $7 D003577
- 650 _2
- $a dexamethason $x farmakologie $7 D003907
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a hepatocytární jaderný faktor 4 $x fyziologie $7 D051557
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a P-glykoprotein $x biosyntéza $7 D020168
- 650 _2
- $a těhotenství $7 D011247
- 650 _2
- $a promotorové oblasti (genetika) $x fyziologie $7 D011401
- 650 _2
- $a messenger RNA $x metabolismus $7 D012333
- 650 _2
- $a receptory glukokortikoidů $x fyziologie $7 D011965
- 650 _2
- $a aktivace transkripce $x fyziologie $7 D015533
- 650 _2
- $a trofoblasty $x metabolismus $7 D014327
- 650 _2
- $a financování organizované $7 D005381
- 655 _2
- $a srovnávací studie $7 D003160
- 700 1_
- $a Červený, Lukáš $7 xx0098555
- 700 1_
- $a Krausová, Lucie. $7 xx0122166
- 700 1_
- $a Brysch, M
- 700 1_
- $a Libra, Antonín. $7 _BN007788
- 700 1_
- $a Vrzal, Radim $7 xx0118949
- 700 1_
- $a Nachtigal, Petr $7 uk2009304471
- 700 1_
- $a Štaud, František, $d 1970- $7 stk2007393932
- 700 1_
- $a Ulrichová, Jitka, $d 1956- $7 ola2002158251
- 700 1_
- $a Fendrich, Zdeněk, $d 1942- $7 jk01030904
- 700 1_
- $a Dvořák, Zdeněk, $d 1974- $7 xx0118950
- 773 0_
- $w MED00003835 $t Placenta $g Roč. 28, č. 10 (2007), s. 1004-1011 $x 0143-4004
- 910 __
- $a ABA008 $b x $y 7
- 990 __
- $a 20100826150022 $b ABA008
- 991 __
- $a 20120713143141 $b ABA008
- 999 __
- $a ok $b bmc $g 749112 $s 612733
- BAS __
- $a 3
- BMC __
- $a 2007 $b 28 $c 10 $d 1004-1011 $i 0143-4004 $m Placenta $n Placenta $x MED00003835
- LZP __
- $a 2010-B2/ipme