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Time- and Dose-Dependent Effects of 17 Beta-Estradiol on Short-Term, Real-Time Proliferation and Gene Expression in Porcine Granulosa Cells
S. Ciesiółka, J. Budna, K. Jopek, A. Bryja, W. Kranc, S. Borys, M. Jeseta, A. Chachuła, A. Ziółkowska, P. Antosik, D. Bukowska, KP. Brüssow, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Hindawi Publishing Open Access od 2001-01-01
PubMed Central od 2013
Europe PubMed Central od 2013
ProQuest Central od 2013
Open Access Digital Library od 2001-01-01
Open Access Digital Library od 2012-12-04
Open Access Digital Library od 2013-01-01
CINAHL Plus with Full Text (EBSCOhost) od 2013-01-01
Medline Complete (EBSCOhost) od 2013-01-01
Health & Medicine (ProQuest) od 2013
ROAD: Directory of Open Access Scholarly Resources od 2013
Odkazy
PubMed
28337462
DOI
10.1155/2017/9738640
Knihovny.cz E-zdroje
- MeSH
- buněčná diferenciace účinky léků genetika MeSH
- estradiol aplikace a dávkování MeSH
- folikulární buňky účinky léků metabolismus MeSH
- IVM techniky MeSH
- lidé MeSH
- oocyty účinky léků růst a vývoj MeSH
- oogeneze účinky léků genetika MeSH
- prasata MeSH
- proliferace buněk účinky léků MeSH
- receptory FSH biosyntéza genetika MeSH
- receptory LH biosyntéza genetika MeSH
- rodina 19 cytochromů P450 biosyntéza MeSH
- vývojová regulace genové exprese účinky léků MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
The key mechanisms responsible for achievement of full reproductive and developmental capability in mammals are the differentiation and transformation of granulosa cells (GCs) during folliculogenesis, oogenesis, and oocyte maturation. Although the role of 17 beta-estradiol (E2) in ovarian activity is widely known, its effect on proliferative capacity, gap junction connection (GJC) formation, and GCs-luteal cells transformation requires further research. Therefore, the goal of this study was to assess the real-time proliferative activity of porcine GCs in vitro in relation to connexin (Cx), luteinizing hormone receptor (LHR), follicle stimulating hormone receptor (FSHR), and aromatase (CYP19A1) expression during short-term (168 h) primary culture. The cultured GCs were exposed to acute (at 96 h of culture) and/or prolonged (between 0 and 168 h of culture) administration of 1.8 and 3.6 μM E2. The relative abundance of Cx36, Cx37, Cx40, Cx43, LHR, FSHR, and CYP19A1 mRNA was measured. We conclude that the proliferation capability of GCs in vitro is substantially associated with expression of Cxs, LHR, FSHR, and CYP19A1. Furthermore, the GC-luteal cell transformation in vitro may be significantly accompanied by the proliferative activity of GCs in pigs.
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- $a Ciesiółka, Sylwia $u Department of Histology and Embryology, Poznan University of Medical Sciences, 6 Święcickiego St., 60-781 Poznań, Poland.
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- $a Time- and Dose-Dependent Effects of 17 Beta-Estradiol on Short-Term, Real-Time Proliferation and Gene Expression in Porcine Granulosa Cells / $c S. Ciesiółka, J. Budna, K. Jopek, A. Bryja, W. Kranc, S. Borys, M. Jeseta, A. Chachuła, A. Ziółkowska, P. Antosik, D. Bukowska, KP. Brüssow, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,
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- $a The key mechanisms responsible for achievement of full reproductive and developmental capability in mammals are the differentiation and transformation of granulosa cells (GCs) during folliculogenesis, oogenesis, and oocyte maturation. Although the role of 17 beta-estradiol (E2) in ovarian activity is widely known, its effect on proliferative capacity, gap junction connection (GJC) formation, and GCs-luteal cells transformation requires further research. Therefore, the goal of this study was to assess the real-time proliferative activity of porcine GCs in vitro in relation to connexin (Cx), luteinizing hormone receptor (LHR), follicle stimulating hormone receptor (FSHR), and aromatase (CYP19A1) expression during short-term (168 h) primary culture. The cultured GCs were exposed to acute (at 96 h of culture) and/or prolonged (between 0 and 168 h of culture) administration of 1.8 and 3.6 μM E2. The relative abundance of Cx36, Cx37, Cx40, Cx43, LHR, FSHR, and CYP19A1 mRNA was measured. We conclude that the proliferation capability of GCs in vitro is substantially associated with expression of Cxs, LHR, FSHR, and CYP19A1. Furthermore, the GC-luteal cell transformation in vitro may be significantly accompanied by the proliferative activity of GCs in pigs.
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