• 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

. 2007 ; 28 (10) : 1004-1011.

Jazyk angličtina Země Velká Británie

Typ dokumentu srovnávací studie

Perzistentní odkaz   https://www.medvik.cz/link/bmc10013238

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

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...