Key Laboratory for Regenerative Medicine (JNU-CUHK)Ministry of Education, Department of Developmental and Regenerative Biology, College of Life Science and Technologies, Jinan University, Guangzhou, China.
Department of Reproductive MedicineThe First Affiliated Hospital, Jinan University, Guangzhou, China.
Reproduction. 2018 Apr;155(4):333-346. doi: 10.1530/REP-17-0783. Epub 2018 Feb 1.
C1q/tumor necrosis factor-related protein 3 (C1QTNF3) is a novel adipokine with modulating effects on metabolism, inflammation and the cardiovascular system. C1QTNF3 expression levels in the sera and omental adipose tissues of women with PCOS are low compared to control subjects. However, the expression and function of C1QTNF3 in the ovary has not previously been examined. Here, we assessed the expression patterns of in the ovary and explored its role in folliculogenesis. The transcript abundance was higher in large follicles than in small follicles and was under the influence of gonadotropin. C1QTNF3 was detected mainly in the granulosa cells and oocytes of growing follicles and modestly in the granulosa cells of atretic follicles and in luteal cells. Excess androgen significantly decreased C1QTNF3 expression in the ovaries and in granulosa cells Recombinant C1QTNF3 protein accelerated the weight gain of ovarian explants and the growth of preantral follicles induced by follicle stimulating hormone (FSH) The stimulatory effect of C1QTNF3 on ovarian growth was accompanied by the initiation of AKT, mTOR, p70S6K and 4EBP1 phosphorylation, an increase in CCND2 expression and a reduction in cleaved CASP3 levels. Moreover, the addition of C1QTNF3 accelerated proliferation and reduced activated CASP3/7 activity in granulosa cells. , the ovarian intrabursal administration of the C1QTNF3 antibody delayed gonadotropin-induced antral follicle development. Taken together, our data demonstrate that C1QTNF3 is an intraovarian factor that promotes follicle growth by accelerating proliferation, decelerating apoptosis and promoting AKT/mTOR phosphorylation.
C1q/肿瘤坏死因子相关蛋白 3(C1QTNF3)是一种新型脂肪因子,具有调节代谢、炎症和心血管系统的作用。与对照组相比,多囊卵巢综合征(PCOS)女性血清和网膜脂肪组织中的 C1QTNF3 表达水平较低。然而,C1QTNF3 在卵巢中的表达和功能尚未被检测到。在这里,我们评估了 C1QTNF3 在卵巢中的表达模式,并探讨了其在卵泡发生中的作用。C1QTNF3 的转录丰度在大卵泡中高于小卵泡,且受促性腺激素的影响。C1QTNF3 主要在生长卵泡的颗粒细胞和卵母细胞中检测到,在闭锁卵泡的颗粒细胞和黄体细胞中检测到少量。过量雄激素显著降低卵巢中 C1QTNF3 的表达 ,并在颗粒细胞中降低 C1QTNF3 的表达。重组 C1QTNF3 蛋白加速卵巢外植体的增重和促卵泡激素(FSH)诱导的原始卵泡生长。C1QTNF3 对卵巢生长的刺激作用伴随着 AKT、mTOR、p70S6K 和 4EBP1 磷酸化的启动、CCND2 表达的增加和 cleaved CASP3 水平的降低。此外,C1QTNF3 的添加加速了颗粒细胞的增殖并降低了激活的 CASP3/7 活性。此外,C1QTNF3 抗体在卵巢内的注射延迟了促性腺激素诱导的窦卵泡发育。总之,我们的数据表明,C1QTNF3 是一种卵巢内因子,通过加速增殖、减缓凋亡和促进 AKT/mTOR 磷酸化来促进卵泡生长。