2017
Time- and Dose-Dependent Effects of 17 Beta-Estradiol on Short-Term, Real-Time Proliferation and Gene Expression in Porcine Granulosa Cells
CIESIÓŁKA, Sylwia; Joanna BUDNA; Karol JOPEK; Artur BRYJA; Wiesława KRANC et al.Základní údaje
Originální název
Time- and Dose-Dependent Effects of 17 Beta-Estradiol on Short-Term, Real-Time Proliferation and Gene Expression in Porcine Granulosa Cells
Autoři
CIESIÓŁKA, Sylwia; Joanna BUDNA; Karol JOPEK; Artur BRYJA; Wiesława KRANC; Sylwia BORYS; Michal JEŠETA; Adrian CHACHUŁA; Agnieszka ZIÓŁKOWSKA; Paweł ANTOSIK; Dorota BUKOWSKA; Klaus P. BRÜSSOW; Małgorzata BRUSKA; Michał NOWICKI; Maciej ZABEL a Bartosz KEMPISTY
Vydání
Biomed Research International, New York, Hindawi Publishing Corporation, 2017, 2314-6133
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30400 3.4 Medical biotechnology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.583
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/17:00096491
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
CELLULAR-DISTRIBUTION; CUMULUS CELLS; FOLLICULAR DEVELOPMENT; PROTEIN EXPRESSION; OOCYTE; PROGESTERONE; ESTROGEN; CONNEXIN-43; COMPETENCE; CX43
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 21. 3. 2018 16:43, Soňa Böhmová
Anotace
V originále
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 oocytematuration. Although the role of 17 beta-estradiol (E2) in ovarian activity is widely known, its effect on proliferative capacity, gap junction connection (GJC) formation, andGCs-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.. mu M E2. The relative abundance of Cx36, Cx37, Cx40, Cx43, LHR, FSHR, and CYP19A1mRNA wasmeasured. We conclude that the proliferation capability of GCs in vitro is substantially associated with expression of Cxs, LHR, FSHR, andCYP19A1. Furthermore, the GC-luteal cell transformation in vitro may be significantly accompanied by the proliferative activity of GCs in pigs.