Tukur Hammed A, Aljumaah Riyadh S, Swelum Ayman Abdel-Aziz, N Alowaimer Abdullah, Abdelrahman Mutassim, Saadeldin Islam M
Department of Animal Production, College of Food and Agricultural Sciences, King Saud University, Riyadh 11451, Saudi Arabia.
Department of Theriogenology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.
Animals (Basel). 2020 Apr 25;10(5):750. doi: 10.3390/ani10050750.
This is the first report on a biphasic in vitro maturation (IVM) approach with a meiotic inhibitor to improve dromedary camel IVM. Spontaneous meiotic resumption poses a major setback for in vitro matured oocytes. The overall objective of this study was to improve in vitro maturation of dromedary camel oocytes using ROCK inhibitor (Y-27632) in a biphasic IVM to prevent spontaneous meiotic resumption. In the first experiment, we cultured immature cumulus-oocyte complexes (COCs, = 375) in a prematuration medium supplemented with ROCK inhibitor (RI) for 2 h, 4 h, 6 h, and 24 h before submission to normal in vitro maturation to complete 28 h. The control was cultured for 28 h in the absence of RI. In the first phase of experiment two, we cultured COCs ( = 480) in the presence or absence (control) of RI for 2 h, 4 h, 6 h, and 24 h, and conducted real-time relative quantitative PCR (qPCR) on selected mRNA transcripts. The same was done in the second phase, but qPCR was done after completion of normal IVM. Assessment of nuclear maturation showed that pre-IVM for 4 h yielded an increase in MII oocyte (54.67% vs. 26.6% of control; < 0.05). As expected, the same group showed the highest degree (2) of cumulus expansion. In experiment 2, qPCR results showed significantly higher expression of and in the RI group treated for 4 h when compared with the other groups. However, their relative quantification after biphasic IVM did not reveal any significant difference, except for the positive response of and ratio after 4 and 6 h biphasic IVM. In conclusion, RI prevents premature oocyte maturation and gave a significantly positive outcome during the 4 h treatment. This finding is a paradigm for future investigation on dromedary camel biphasic IVM and for improving the outcome of IVM in this species.
这是关于一种采用减数分裂抑制剂的双相体外成熟(IVM)方法以改善单峰骆驼IVM的首次报告。自发减数分裂恢复是体外成熟卵母细胞面临的一个主要障碍。本研究的总体目标是在双相IVM中使用ROCK抑制剂(Y - 27632)来改善单峰骆驼卵母细胞的体外成熟,以防止自发减数分裂恢复。在第一个实验中,我们将未成熟的卵丘 - 卵母细胞复合体(COCs,n = 375)在添加了ROCK抑制剂(RI)的预成熟培养基中培养2小时、4小时、6小时和24小时,然后进行正常的体外成熟28小时。对照组在无RI的情况下培养28小时。在实验二的第一阶段,我们将COCs(n = 480)在有或无(对照)RI的情况下培养2小时、4小时、6小时和24小时,并对选定的mRNA转录本进行实时相对定量PCR(qPCR)。第二阶段也进行同样的操作,但qPCR在正常IVM完成后进行。核成熟评估表明,预IVM 4小时使MII期卵母细胞增加(54.67%对对照组的26.6%;P < 0.05)。正如预期的那样,同一组显示出最高程度(2级)的卵丘扩展。在实验2中,qPCR结果显示,与其他组相比,在4小时处理的RI组中,[具体基因名称1]和[具体基因名称2]的表达显著更高。然而,双相IVM后的相对定量除了在4小时和6小时双相IVM后[具体基因名称1]和[具体基因名称2]的比率有阳性反应外,未显示出任何显著差异。总之,RI可防止卵母细胞过早成熟,并且在4小时处理期间产生了显著的阳性结果。这一发现为未来关于单峰骆驼双相IVM的研究以及改善该物种IVM的结果提供了范例。