Ni Hemin, Sheng Xihui, Cui Xu, Gu Meichao, Liu Yunhai, Qi Xiaolong, Xing Shuhan, Guo Yong
Animal Science and Technology College, Beijing University of Agriculture, Beijing, China.
PLoS One. 2015 Mar 23;10(3):e0120418. doi: 10.1371/journal.pone.0120418. eCollection 2015.
Epidermal growth factor (EGF) has been shown to facilitate the in vitro maturation of sheep oocytes, and enhance embryo's capability for further development. However, such kind of molecular mechanism has not yet been elucidated. In the present study, we investigated the effect of EGF-mediated mitogen-activated protein kinases 3 and 1 (MAPK3/1) pathway on in vitro maturation of sheep oocytes. U0126, a specific inhibitor of MEK (MAPK kinase), was added into the maturation culture medium to block the EGF-mediated MAPK3/1 pathway with different doses. Then, the nuclear maturation of sheep oocytes was examined. Additionally, the effect of EGF-mediated MAPK3/1 on cytoplasmic maturation was examined though in vitro fertilization and embryonic development. The rate of germinal vesicle breakdown (GVBD) after 6 h of culture with 10⁻⁴ mol/l of U0126 (50.4%) was significantly decreased compared with control (67.2%, p < 0.05), and the first polation body (PB1) extrusion rate after 22 h of culture in drug treatment was also significantly inhibited compared with control (28.6% vs. 48.4%, p < 0.05). However, 10-6 mol/l U0126 had slight effect on oocyte nuclear maturation. The normal distribution rate of α-tubulin in the oocytes after 22 h of in vitro maturation was significantly decreased in the 10⁻⁴ mol/l U0126 group (54%) compared with control (68%, p < 0.05). After in vitro fertilization, the cleavage rate in drug treatments (56.8% in 10⁻⁶ mol/l U0126 group and 42.6% in 10⁻⁴ mol/l U0126 group) was significantly decreased compared with control (72.3%, p < 0.01). The blastocyst rate in 10⁻⁴ mol/l U0126 group (17.6%) was also significantly decreased compared with control (29.9%, p < 0.05). Collectively, these results suggest that EGF-mediated MAPK3/1 pathway is conducive to in vitro maturation of sheep oocytes.
表皮生长因子(EGF)已被证明可促进绵羊卵母细胞的体外成熟,并增强胚胎的进一步发育能力。然而,这种分子机制尚未阐明。在本研究中,我们研究了EGF介导的丝裂原活化蛋白激酶3和1(MAPK3/1)信号通路对绵羊卵母细胞体外成熟的影响。将MEK(MAPK激酶)的特异性抑制剂U0126以不同剂量添加到成熟培养基中,以阻断EGF介导的MAPK3/1信号通路。然后,检测绵羊卵母细胞的核成熟情况。此外,通过体外受精和胚胎发育检测EGF介导的MAPK3/1对细胞质成熟的影响。与对照组相比,用10⁻⁴mol/L U0126培养6小时后的生发泡破裂(GVBD)率(50.4%)显著降低(对照组为67.2%,p<0.05),药物处理组培养22小时后的第一极体(PB1)排出率也与对照组相比显著受到抑制(28.6%对48.4%,p<0.05)。然而,10⁻⁶mol/L U0126对卵母细胞核成熟影响轻微。与对照组(68%,p<0.05)相比,10⁻⁴mol/L U0126组体外成熟22小时后卵母细胞中α-微管蛋白的正常分布率显著降低(54%)。体外受精后,与对照组(72.3%,p<0.01)相比,药物处理组的卵裂率显著降低(10⁻⁶mol/L U0126组为56.8%,10⁻⁴mol/L U0126组为42.6%)。10⁻⁴mol/L U0126组的囊胚率(17.6%)也与对照组(29.9%,p<0.05)相比显著降低。总体而言,这些结果表明EGF介导的MAPK3/1信号通路有利于绵羊卵母细胞的体外成熟。