College of Animal Science and Technology, Hebei Agricultural University, Baoding Hebei 071001, China.
College of Veterinary Medicine, Hebei Agricultural University, Baoding Hebei 071001, China.
Poult Sci. 2020 Nov;99(11):6147-6162. doi: 10.1016/j.psj.2020.08.001. Epub 2020 Aug 26.
Melatonin is a key regulator of follicle granular cell maturation and ovulation. The mammalian target of rapamycin (mTOR) pathway plays an important role in cell growth regulation. Therefore, our aim was to investigate whether the mTOR signaling pathway is involved in the regulation of melatonin-mediated proliferation and apoptotic mechanisms in granulosa cells. Chicken follicle granular cells were cultured with melatonin (0, 2, 20, or 200 μmol/L) for 48 h. The results showed that melatonin treatment enhanced proliferation and suppressed apoptosis in granular cells at 20 μmol/L and 200 μmol/L (P < 0.05) by upregulation of cyclin D1 (P < 0.01) and Bcl-2 (P < 0.01) and downregulation of P21, caspase-3, Beclin1, and LC3-II (P < 0.01). The effects resulted in the activation of the mTOR signaling pathway by increasing the expression of avTOR, PKC, 4E-BP1, S6K (P < 0.05), p-mTOR, and p-S6K. We added an mTOR activator and inhibitor to the cells and identified the optimal dose (10 μmol/L MHY1485 and 100 nmol/L rapamycin) for subsequent experiments. The combination of 20 μmol/L melatonin and 10 μmol/L MHY1485 significantly enhanced granulosa cell proliferation (P < 0.05), while 100 nmol/L rapamycin significantly inhibited proliferation and enhanced apoptosis (P < 0.05), but this action was reversed in the 20-μmol/L melatonin and 100-nmol/L rapamycin cotreatment groups (P < 0.05). This was confirmed by mRNA and protein expression that was associated with proliferation, apoptosis, and autophagy (P < 0.05). The combination of 20 μmol/L melatonin and 10 μmol/L MHY1485 also activated the mTOR pathway upstream genes PI3K, AKT1, and AKT2 and downstream genes PKC, 4E-BP1, and S6K (P < 0.05), as well as protein expression of p-mTOR and p-S6K. Rapamycin significantly inhibited the mTOR pathway-related genes mRNA levels (P < 0.05). In addition, activation of the mTOR pathway increased melatonin receptor mRNA levels (P < 0.05). In conclusion, these findings demonstrate that melatonin regulates chicken granulosa cell proliferation and apoptosis by activating the mTOR signaling pathway via its receptor.
褪黑素是卵泡颗粒细胞成熟和排卵的关键调节剂。哺乳动物雷帕霉素靶蛋白(mTOR)途径在细胞生长调节中起着重要作用。因此,我们的目的是研究 mTOR 信号通路是否参与调节褪黑素介导的颗粒细胞增殖和凋亡机制。鸡卵泡颗粒细胞用褪黑素(0、2、20 或 200 μmol/L)培养 48 h。结果表明,褪黑素在 20 μmol/L 和 200 μmol/L 时通过上调细胞周期蛋白 D1(P < 0.01)和 Bcl-2(P < 0.01)以及下调 P21、caspase-3、Beclin1 和 LC3-II(P < 0.01)增强颗粒细胞的增殖并抑制凋亡。这种作用导致 mTOR 信号通路的激活,增加 avTOR、PKC、4E-BP1、S6K 的表达(P < 0.05),p-mTOR 和 p-S6K。我们向细胞中添加了 mTOR 激活剂和抑制剂,并确定了后续实验的最佳剂量(10 μmol/L MHY1485 和 100 nmol/L 雷帕霉素)。20 μmol/L 褪黑素和 10 μmol/L MHY1485 的组合显著增强了颗粒细胞的增殖(P < 0.05),而 100 nmol/L 雷帕霉素显著抑制增殖并增强凋亡(P < 0.05),但在 20 μmol/L 褪黑素和 100 nmol/L 雷帕霉素共同处理组中这种作用被逆转(P < 0.05)。这通过与增殖、凋亡和自噬相关的 mRNA 和蛋白质表达得到证实(P < 0.05)。20 μmol/L 褪黑素和 10 μmol/L MHY1485 的组合还激活了 mTOR 途径的上游基因 PI3K、AKT1 和 AKT2 以及下游基因 PKC、4E-BP1 和 S6K(P < 0.05),以及 p-mTOR 和 p-S6K 的蛋白表达。雷帕霉素显著抑制 mTOR 途径相关基因的 mRNA 水平(P < 0.05)。此外,mTOR 途径的激活增加了褪黑素受体 mRNA 水平(P < 0.05)。总之,这些发现表明褪黑素通过其受体激活 mTOR 信号通路来调节鸡颗粒细胞的增殖和凋亡。