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通过玻璃化冷冻在生发泡期的卵母细胞进行体外受精生产高质量的猪囊胚。

Production of good-quality porcine blastocysts by in vitro fertilization of follicular oocytes vitrified at the germinal vesicle stage.

机构信息

Division of Animal Sciences, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki, Japan.

出版信息

Theriogenology. 2010 Jan 15;73(2):147-56. doi: 10.1016/j.theriogenology.2009.08.008.

Abstract

We investigated survival, meiotic competence, cytoplasmic maturation, in vitro fertilization, and development of immature porcine (Sus scrofa) oocytes cryopreserved by a modified solid surface vitrification protocol. Cumulus-oocyte complexes (COCs) collected from follicles 3 to 6mm in diameter in abattoir-derived ovaries of prepubertal gilts were either vitrified (Vitrified group), subjected to cryoprotectant treatment (CPA group), or used without any treatment (Control group). Oocyte viability was assayed by staining with fluorescein diacetate. Live oocytes were matured in vitro and their meiotic progression investigated by nuclear staining. In a series of experiments, the glutathione (GSH) content of in vitro-matured oocytes and viability of cumulus cells were assayed simultaneously. The in vitro-matured oocytes were also fertilized and cultured in vitro to assess their ability to be fertilized and to develop to the blastocyst stage, respectively. The proportion of viable oocytes in the Vitrified group was significantly lower than that in the CPA and Control groups (27.7%, 90.4%, and 100%, respectively). Among the three groups, there were no differences in meiotic competence, cumulus viability, and GSH levels at the end of in vitro maturation. Fertilization parameters (i.e., rates of male pronucleus formation, monospermy, and second polar body extrusion) were also similar among groups. However, comparison of the developmental abilities of oocytes in the Vitrified, CPA, and Control groups revealed that the Vitrified group had a significantly reduced ability to undergo first cleavage (34.4%, 63.3%, and 69.0%) and to develop to the blastocyst stage (5.1%, 25.5%, and 34.6%). The mean total cell numbers in blastocysts after 6 d of culture were not significantly different among the Vitrified, CPA, and Control groups (40.3, 42.8, and 43.4). In conclusion, despite low survival rates and impaired development in the Vitrified group, meiotic competence, cytoplasmic maturation, and subsequent fertilization characteristics of surviving germinal vesicle oocytes were unaffected by vitrification, and high-quality blastocysts were produced from vitrified immature oocytes.

摘要

我们研究了通过改良的固相玻璃化方案冷冻保存的不成熟猪(Sus scrofa)卵母细胞的存活率、减数分裂能力、细胞质成熟度、体外受精和发育情况。从屠宰场来源的青春期小母猪卵巢中直径为 3 至 6mm 的卵泡中收集卵丘-卵母细胞复合物(COCs),要么进行玻璃化(玻璃化组),要么进行冷冻保护剂处理(CPA 组),要么不进行任何处理(对照组)。通过用荧光二乙酸酯染色来检测卵母细胞的活力。将活卵母细胞在体外成熟,并通过核染色研究其减数分裂进展。在一系列实验中,同时检测体外成熟卵母细胞的谷胱甘肽(GSH)含量和卵丘细胞的活力。体外成熟的卵母细胞也进行受精和体外培养,以分别评估其受精能力和发育至囊胚阶段的能力。玻璃化组中活卵母细胞的比例明显低于 CPA 组和对照组(分别为 27.7%、90.4%和 100%)。在这三组中,减数分裂能力、卵丘细胞活力和体外成熟结束时的 GSH 水平没有差异。受精参数(即雄性原核形成率、单精子受精率和第二极体排出率)在组间也相似。然而,比较玻璃化组、CPA 组和对照组卵母细胞的发育能力发现,玻璃化组的第一次卵裂能力显著降低(分别为 34.4%、63.3%和 69.0%),并且发育到囊胚阶段的能力也显著降低(分别为 5.1%、25.5%和 34.6%)。体外培养 6 天后囊胚的总细胞数在玻璃化组、CPA 组和对照组之间没有显著差异(分别为 40.3、42.8 和 43.4)。总之,尽管玻璃化组的存活率低且发育受损,但玻璃化并未影响存活的生发泡期卵母细胞的减数分裂能力、细胞质成熟度和随后的受精特征,并且从玻璃化的不成熟卵母细胞中产生了高质量的囊胚。

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