Involvement of peroxisome proliferator-activated receptors in the estradiol production of ovine Sertoli cells

  • سال انتشار: 1396
  • محل انتشار: گفتمان پژوهش دامپزشکی، دوره: 8، شماره: 3
  • کد COI اختصاصی: JR_VRFAN-8-3_011
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 60
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نویسندگان

Hossein Hassanpour

Department of Gamete and Cloning, Research Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran

Valiallah Khalaji-Pirbalouty

Department of Biology, Faculty of Science, Shahrekord University, Shahrekord, Iran

Manoochehr Adibi

Department of Biology, Faculty of Science, Shahrekord University, Shahrekord, Iran

Hassan Nazari

Department of Gamete and Cloning, Research Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran

چکیده

Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors of transcription factors composed of three family members: PPARα, PPARβ/δ and PPARγ. This study was aimed to evaluate the role of PPARs in the estradiol production via follicle stimulating hormone (FSH) in the ovine Sertoli cells. At the first step, transcripts of PPARα, PPARβ /δ and PPARγ were evaluated by quantitative real time PCR (qRT-PCR) in the ovine Sertoli cells in vitro after FSH treatment. PPARγ transcript was increased in FSH-treated cells while PPARα and PPAR β /δ transcripts were unchanged. At the second step, Pioglitazone as PPARγ agonist and ۲-chloro-۵-nitrobenzanilide (GW۹۶۶۲) as PPARγ antagonist were used in the FSH-treated Sertoli cells and then, the estradiol production and aromatase transcript were evaluated. Aromatase transcript was increased by pioglitazone in the FSH-treated Sertoli cells while GW۹۶۶۲ did not change its transcript. The estradiol production was increased by low concentrations of pioglitazone in FSH-treated Sertoli cells while the production of this hormone was decreased by the high concentration of Pioglitazone. The GW۹۶۶۲ did not change the production of estradiol in FSH-treated Sertoli cells. It is concluded that FSH regulates the estradiol production and aromatase expression in a way independently of PPARβ/δ and PPARα activation, although FSH increases the transcript of PPARγ and in this way, it could affect (mostly increase) aromatase transcript and estradiol production. Probably, this effect of FSH in the estradiol production via PPARγ is only a servo-assist mechanism which if it was inhibited, the estradiol production was not considerably affected.

کلیدواژه ها

Aromatase, Estradiol, PPAR, Sertoli cell, Sheep

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