Institute for Stem Cell and Regenerative Medicine (ISCRM), College of Veterinary Medicine, Chungbuk National University, Cheongju, 28644, Republic of Korea; Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University, Cheongju, 28644, Republic of Korea; Department of Medicine, Surgery and Obstetrics, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Barishal Campus, Barisal, 8210, Bangladesh.
Institute for Stem Cell and Regenerative Medicine (ISCRM), College of Veterinary Medicine, Chungbuk National University, Cheongju, 28644, Republic of Korea; Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University, Cheongju, 28644, Republic of Korea.
Theriogenology. 2024 Apr 1;218:16-25. doi: 10.1016/j.theriogenology.2024.01.020. Epub 2024 Jan 24.
Numerous growth factors contribute to oocyte maturation and embryonic development in vivo; however, only a few are understood. One such factor is epigen, a new member of the epidermal growth factor (EGF) family that is secreted by the granulosa cells of immature oocytes. We hypothesized that epigen may play a role in oocyte maturation, specifically in the nuclear and cytoplasmic aspects. This study aimed to investigate the effects of epigen on porcine oocyte maturation and embryo development in vitro. In this study, three different concentrations of epigen (3, 6, and 30 ng/mL) were added to tissue culture medium-199 (TCM-199) during in vitro maturation of porcine oocytes. A control group that did not receive epigen supplementation was also included. Mature porcine oocytes were fertilized, and the resulting zygotes were cultured until day 7. The levels of intracellular glutathione (GSH) and reactive oxygen species (ROS) were measured in the in vitro matured oocytes. At the same time, the expression patterns of genes related to apoptosis were detected in day 7 blastocysts (BLs) using real-time quantitative PCR Apoptosis was detected by annexin-V assays in mature oocytes. Data were analyzed using ANOVA and Duncan's test on SPSS, and results are presented as mean ± SEM. The group that received 6 ng/mL epigen had a significantly lower rate of germinal vesicle breakdown (GVBD) than the control group without affecting the nuclear maturation among the experimental groups. Among the treatment groups, the 6 ng/mL epigen group showed significantly higher levels of intracellular GSH and lower ROS production. Supplementation with 6 ng/mL epigen significantly improved blastocyst (BL) formation rates compared to those in the control and 3 ng/mL groups. Additionally, the blastocyst expansion rate was significantly higher with epigen supplementation (6 ng/mL). In the fertilization experiment, the group supplemented with 6 ng/mL epigen exhibited significantly higher levels of monospermy and fertilization efficiency and lower levels of polyspermy than the control group. This study indicated that adding epigen at a concentration of 6 ng/mL can significantly enhance the developmental potential of porcine oocytes fertilized in vitro. Specifically, the study found that epigen improves cytoplasmic maturation, which helps prevent polyspermy and emulates monospermic penetration.
许多生长因子有助于卵母细胞在体内成熟和胚胎发育;然而,只有少数几种生长因子被人们所了解。表皮生长因子(EGF)家族的一个新成员——epigen 就是其中之一,它由不成熟卵母细胞的颗粒细胞分泌。我们假设 epigen 可能在卵母细胞成熟过程中发挥作用,特别是在核和细胞质方面。本研究旨在探讨 epigen 对猪卵母细胞体外成熟和胚胎发育的影响。在这项研究中,在猪卵母细胞体外成熟过程中,将三种不同浓度的 epigen(3、6 和 30ng/ml)添加到组织培养液-199(TCM-199)中。同时,还包括一个未添加 epigen 的对照组。成熟的猪卵母细胞受精后,将得到的受精卵培养至第 7 天。测量体外成熟卵母细胞中的细胞内谷胱甘肽(GSH)和活性氧(ROS)水平。同时,使用实时定量 PCR 检测第 7 天囊胚(BL)中与凋亡相关的基因表达模式。通过 Annexin-V 测定法检测成熟卵母细胞中的凋亡。使用 SPSS 的 ANOVA 和 Duncan 检验对数据进行分析,结果以平均值±SEM 表示。与对照组相比,接受 6ng/ml epigen 的组卵母细胞的生发泡破裂(GVBD)率显著降低,但实验组之间的核成熟不受影响。在处理组中,6ng/ml epigen 组的细胞内 GSH 水平显著升高,ROS 产生量降低。与对照组和 3ng/ml 组相比,添加 6ng/ml epigen 显著提高了囊胚(BL)形成率。此外,添加 epigen 可显著提高囊胚的扩张率(6ng/ml)。在受精实验中,与对照组相比,添加 6ng/ml epigen 的组的单精受精率和受精效率显著提高,多精受精率显著降低。本研究表明,在浓度为 6ng/ml 时添加 epigen 可以显著提高体外受精的猪卵母细胞的发育潜力。具体来说,该研究发现 epigen 改善了细胞质成熟,有助于防止多精受精,并模拟了单精穿透。