Zhang Tong, Fan Xiaomei, Li Ruilan, Zhang Chunqiang, Zhang Jiaxin
Key Laboratory of Animal Genetics, Breeding and Reproduction, College of Animal Science, Inner Mongolia Agricultural University, Hohhot 010018, Inner Mongolia, China.
Basic Medical College, Inner Mongolia Medical University, Hohhot 010110, Inner Mongolia, China.
Biochem Biophys Res Commun. 2018 Feb 26;497(1):200-206. doi: 10.1016/j.bbrc.2018.02.054. Epub 2018 Feb 8.
In vitro produced mammalian embryos suffer from developmental failure, with a large proportion showing embryonic retardation, degradation, or apoptosis. This failure is due, in part, to incomplete oocyte cytoplasmic maturation. C-type natriuretic peptide (CNP) has been reported to act as a meiotic inhibitor. Here we explored the potential effects of CNP pre-treatment sheep oocytes on nuclear maturation, changes in mitochondrial behavior and developmental competence of in vitro fertilized embryos. Sheep cumulus-oocyte complexes (COCs) were aspirated from abattoir-derived ovaries. Nuclear progression was assessed using DAPI chromatin staining, the expression of natriuretic peptide receptor 2 (NPR2) was evaluated by RT-qPCR, active mitochondria localization was assessed with a confocal laser scanning microscopy using MitoTracker Red, and the developmental competence of sheep oocytes subjected to one-step IVM or two-step IVM with or without CNP pretreatment was also investigated. Our results showed that 200 nM CNP could effectively maintain meiotic arrest of sheep COCs in vitro within 4 h. Furthermore, NPR2 mRNA was mainly expressed in cumulus cells. COCs pre-treated with 200 nM CNP for 4 h followed by 24 h IVM showed significantly higher (P < 0.05) cleavage rate and blastocyst rate after in vitro fertilization (IVF), and significantly lower (P < 0.05) proportion of DNA-fragmented nuclei in blastocysts when compared to the conventional 24 h IVM (standard IVM). Non-matured oocytes mainly displayed brilliant circumferential and fine diffuse distribution of mitochondria throughout the cytoplasm. By comparison, 200 nM CNP pre-treated COCs for 4 h led to cytoplasmic mitochondrial granule localization to the peripheral and perinuclear regions. Moreover, oocytes pre-treated with 200 nM CNP for 4 h followed by 24 h IVM, showed mitochondrial organization were similar to those of conventional 24 h matured oocytes in which mitochondria were aggregated more toward the cortical regions of the oocytes, but with larger clumps of stained mitochondria. These results indicate that CNP pre-treatment improves the quality and developmental competence of sheep oocytes and has great potential for facilitating in vitro embryo production.
体外生产的哺乳动物胚胎会出现发育失败,很大一部分表现出胚胎发育迟缓、退化或凋亡。这种失败部分归因于卵母细胞胞质成熟不完全。据报道,C型利钠肽(CNP)可作为减数分裂抑制剂。在此,我们探讨了CNP预处理绵羊卵母细胞对体外受精胚胎的核成熟、线粒体行为变化及发育能力的潜在影响。从屠宰场获取的卵巢中抽吸绵羊卵丘-卵母细胞复合体(COCs)。使用DAPI染色质染色评估核进程,通过RT-qPCR评估利钠肽受体2(NPR2)的表达,使用MitoTracker Red通过共聚焦激光扫描显微镜评估活性线粒体定位,并研究了经过一步体外成熟(IVM)或两步IVM且有无CNP预处理的绵羊卵母细胞的发育能力。我们的结果表明,200 nM CNP可在4小时内有效维持绵羊COCs的减数分裂阻滞。此外,NPR2 mRNA主要在卵丘细胞中表达。与传统的24小时IVM(标准IVM)相比,用200 nM CNP预处理4小时后再进行24小时IVM的COCs在体外受精(IVF)后显示出显著更高(P < 0.05)的卵裂率和囊胚率,以及囊胚中DNA片段化核的比例显著更低(P < 0.05)。未成熟的卵母细胞主要表现出线粒体在整个细胞质中呈明亮的周向和精细的弥散分布。相比之下,用200 nM CNP预处理4小时的COCs导致细胞质线粒体颗粒定位于外周和核周区域。此外,用200 nM CNP预处理4小时后再进行24小时IVM的卵母细胞,其线粒体组织与传统24小时成熟卵母细胞相似,其中线粒体更多地聚集在卵母细胞的皮质区域,但染色的线粒体团块更大。这些结果表明,CNP预处理可提高绵羊卵母细胞的质量和发育能力,在促进体外胚胎生产方面具有巨大潜力。