J 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

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.