Animal Breeding and Reproduction Research Division, Institute of Livestock and Grassland Science, National Agriculture and Food Research Organization, Ibaraki 305-0901, Japan.
Division of Animal Sciences, Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Ibaraki 305-8602, Japan.
J Reprod Dev. 2020 Apr 10;66(2):115-123. doi: 10.1262/jrd.2019-094. Epub 2020 Jan 27.
The aim of the present study was to clarify whether or not our vitrification procedure at the germinal vesicle (GV)-stage triggers the apoptotic cascade in oocytes and subsequent embryos. Immature porcine cumulus-oocyte complexes were either vitrified and warmed (vitrified group) or subjected to cryoprotectant agents (CPA group) or cultured without any treatment (control). Oocytes of all treatment groups were subjected to in vitro maturation (IVM), fertilization, and embryo culture. Apoptosis was assayed in live oocytes at the end of IVM culture and in cleavage-stage embryos after in vitro fertilization (IVF). We detected similar frequencies of DNA fragmentation, levels of caspase activity, phosphatidylserine externalization, and mRNA levels for pro-apoptotic Bax and CASP3 genes in oocytes at the end of IVM and in early embryos among all groups. However, in the vitrified group, the anti-apoptotic Bcl-XL gene was upregulated in 4-8 cell embryos, which caused an 8-fold significant increase in the Bcl-XL/Bax mRNA ratio compared with the control and CPA groups (P < 0.05). In conclusion, vitrification of porcine oocytes at the GV stage by our method did not trigger the apoptotic cascade in oocytes and subsequent embryos but triggered the upregulation of the anti-apoptotic Bcl-XL gene in embryos.
本研究旨在阐明我们在生发泡(GV)期对卵母细胞进行玻璃化处理是否会引发卵母细胞和随后的胚胎发生凋亡级联反应。不成熟的猪卵丘-卵母细胞复合物要么进行玻璃化和复温(玻璃化组),要么用冷冻保护剂(CPA 组)处理,要么不做任何处理(对照组)。所有处理组的卵母细胞都进行体外成熟(IVM)、受精和胚胎培养。在 IVM 培养结束时检测活卵母细胞中的凋亡情况,并在体外受精(IVF)后检测卵裂期胚胎中的凋亡情况。我们在 IVM 培养结束时和早期胚胎中检测到所有组的卵母细胞中 DNA 片段化、半胱天冬酶活性、磷脂酰丝氨酸外翻和促凋亡 Bax 和 CASP3 基因的 mRNA 水平相似。然而,在玻璃化组中,抗凋亡 Bcl-XL 基因在 4-8 细胞胚胎中上调,与对照组和 CPA 组相比,Bcl-XL/Bax mRNA 比值显著增加了 8 倍(P<0.05)。总之,我们的方法对猪卵母细胞进行 GV 期玻璃化处理并没有引发卵母细胞和随后的胚胎发生凋亡级联反应,而是引发了胚胎中抗凋亡 Bcl-XL 基因的上调。