Appeltant Ruth, Somfai Tamás, Santos Elisa C S, Dang-Nguyen Thanh Quang, Nagai Takashi, Kikuchi Kazuhiro
Division of Animal Sciences, Institute of Agrobiological Sciences, National Agriculture and Food Research Organisation, Kannondai 2-1-2, Tsukuba, Ibaraki 305-8602, Japan.
Animal Breeding and Reproduction Research Division, Institute of Livestock and Grassland Science, National Agriculture and Food Research Organisation, Ikenodai 2, Tsukuba, Ibaraki 305-0901, Japan.
Reprod Fertil Dev. 2017 Nov;29(12):2419-2429. doi: 10.1071/RD16386.
Although offspring have been produced from porcine oocytes vitrified at the germinal vesicle (GV) stage, the rate of embryo development remains low. In the present study, nuclear morphology and progression, cumulus expansion, transzonal projections (TZPs), ATP and glutathione (GSH) levels were compared between vitrified cumulus-oocyte complexes (COCs) and control COCs (no cryoprotectant treatment and no cooling), as well as a toxicity control (no cooling). Vitrification was performed with 17.5% (v/v) ethylene glycol and 17.5% (v/v) propylene glycol. Vitrification at the GV stage caused premature meiotic progression, reflected by earlier GV breakdown and untimely attainment of the MII stage. However, cytoplasmic maturation, investigated by measurement of ATP and GSH levels, as well as cumulus expansion, proceeded normally despite detectable damage to TZPs in vitrified COCs. Moreover, treatment with cryoprotectants caused fragmentation of nucleolus precursor bodies and morphological changes in F-actin from which oocytes were able to recover during subsequent IVM culture. Reduced developmental competence may be explained by premature nuclear maturation leading to oocyte aging, although other mechanisms, such as initiation of apoptosis and reduction of cytoplasmic mRNA, can also be considered. Further research will be required to clarify the presence and effects of these phenomena during the vitrification of immature COCs.
尽管已经从在生发泡(GV)期玻璃化的猪卵母细胞中获得了后代,但胚胎发育率仍然很低。在本研究中,比较了玻璃化的卵丘-卵母细胞复合体(COC)与对照COC(未进行冷冻保护剂处理和未冷却)以及毒性对照(未冷却)之间的核形态与进程、卵丘扩展、透明带穿卵突起(TZP)、ATP和谷胱甘肽(GSH)水平。使用17.5%(v/v)乙二醇和17.5%(v/v)丙二醇进行玻璃化处理。GV期玻璃化导致减数分裂过早进行,表现为GV提前破裂和过早达到MII期。然而,通过测量ATP和GSH水平研究的细胞质成熟以及卵丘扩展正常进行,尽管玻璃化的COC中的TZP有可检测到的损伤。此外,冷冻保护剂处理导致核仁前体的碎片化以及F-肌动蛋白的形态变化,卵母细胞在随后的体外成熟培养过程中能够从中恢复。发育能力降低可能是由于过早的核成熟导致卵母细胞老化,尽管也可以考虑其他机制,如凋亡的启动和细胞质mRNA的减少。需要进一步研究来阐明这些现象在未成熟COC玻璃化过程中的存在及影响。