Departament de Ciència Animal i dels Aliments, Facultat de Veterinària, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
Robinson Research Institute, School of Paedriatics and Reproductive Health, The University of Adelaide, Adelaide, South Australia, Australia.
PLoS One. 2019 Aug 23;14(8):e0221663. doi: 10.1371/journal.pone.0221663. eCollection 2019.
In vitro embryo production success in juvenile animals is compromised due to their intrinsic lower oocyte quality. Conventional in vitro maturation (IVM) impairs oocyte competence by inducing spontaneous meiotic resumption. A series of experiments were performed to determine if maintaining meiotic arrest during a pre-maturation culture phase (pre-IVM) prior to conventional IVM improves oocyte competence of juvenile-goat (2 months old) cumulus-oocyte complexes (COCs). In experiment 1, COCs were cultured with C-type natriuretic peptide (CNP; 0, 50, 100, 200 nM) for 6 and 8 h. Nuclear stage was assessed, revealing no differences in the incidence of germinal vesicle (GV) breakdown. In experiment 2, the same CNP concentrations were assessed plus 10 nM estradiol, the known upstream agonist activating expression of NPR2, the exclusive receptor of CNP. CNP (200 nM) plus estradiol increased the rate of oocytes at GV stage at 6 h compared to control group (74.7% vs 28.3%; P<0.05) with predominantly condensed chromatin configuration. In experiment 3, relative mRNA quantification revealed NPR2 expression was down-regulated after pre-IVM (6 h). In experiment 4, analysis of transzonal projections indicated that pre-IVM maintained cumulus-oocyte communication after oocyte recovery. For experiments 5 and 6, biphasic IVM (6 h pre-IVM with CNP and estradiol, plus 24 h IVM) and control IVM (24 h) were compared. Biphasic IVM increased intra-oocyte glutathione and decreased ROS, up-regulated DNA-methyltransferase 1 and pentraxin 3 expression and led to an increase in rate of blastocyst development compared to control group (30.2% vs 17.2%; P<0.05). In conclusion, a biphasic IVM, including a pre-IVM with CNP, maintains oocyte meiotic arrest for 6 h and enhances the embryo developmental competence of oocytes from juvenile goats.
在体外胚胎生产中,由于幼年动物自身卵母细胞质量较低,导致其成功率受到限制。传统的体外成熟(IVM)通过诱导自发减数分裂恢复来损害卵母细胞的能力。进行了一系列实验,以确定在传统 IVM 之前的预成熟培养阶段(预-IVM)中保持减数分裂阻滞是否可以提高幼年山羊(2 个月大)卵丘-卵母细胞复合物(COC)的卵母细胞能力。在实验 1 中,将 COC 用 C 型利钠肽(CNP;0、50、100、200 nM)培养 6 和 8 小时。评估核阶段,发现GV 破裂的发生率没有差异。在实验 2 中,评估了相同的 CNP 浓度加上 10 nM 雌二醇,这是已知的激活 NPR2 表达的上游激动剂,NPR2 是 CNP 的唯一受体。与对照组相比,CNP(200 nM)加雌二醇在 6 小时时增加了处于 GV 阶段的卵母细胞的比例(74.7%比 28.3%;P<0.05),其染色质构型主要为浓缩型。在实验 3 中,相对 mRNA 定量显示预-IVM(6 小时)后 NPR2 表达下调。在实验 4 中,分析透明带投射表明预-IVM 后维持了卵母细胞恢复后的卵丘-卵母细胞通讯。对于实验 5 和 6,比较了双相 IVM(6 小时预-IVM 加 CNP 和雌二醇,加 24 小时 IVM)和对照 IVM(24 小时)。与对照组相比,双相 IVM 增加了卵内谷胱甘肽,减少了 ROS,上调了 DNA-甲基转移酶 1 和五聚蛋白 3 的表达,并导致囊胚发育率增加(30.2%比 17.2%;P<0.05)。总之,包括 CNP 预-IVM 的双相 IVM 可维持卵母细胞减数分裂阻滞 6 小时,并提高幼年山羊卵母细胞的胚胎发育能力。