Casillas Fahiel, Ducolomb Yvonne, Lemus Ana E, Cuello Cristina, Betancourt Miguel
Departamento de Ciencias de la Salud, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana-Iztapalapa, 09340 DF, Mexico; Doctorado en Ciencias Biológicas y de la Salud, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana-Iztapalapa, 09340 DF, Mexico.
Departamento de Ciencias de la Salud, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana-Iztapalapa, 09340 DF, Mexico.
Cryobiology. 2015 Oct;71(2):299-305. doi: 10.1016/j.cryobiol.2015.08.003. Epub 2015 Aug 5.
This study was designed to evaluate the capacity of vitrified-warmed porcine immature oocytes to mature and to be fertilized using in vitro fertilization or intracytoplasmic sperm injection, and to determine the subsequent embryo development. Immature oocytes were vitrified using ethylene glycol and dimethylsulphoxide as cryoprotectants and the Cryolock method. After warming oocytes were cultured 44 h for maturation. Oocytes were randomly distributed in three treatment groups and subjected to in vitro fertilization (Experiment 1) or intracytoplasmic sperm injection (Experiment 2) procedures. The results indicate that the embryo development was higher in denuded oocytes co-cultured with granulosa cells (NkO-CC group) fertilized by in vitro fertilization or intracytoplasmic sperm injection compared to cumulus-cell oocyte complexes (COCs group), showing no significant differences with control. Vitrified denuded oocytes matured with a co-culture system NkO-CC group, displayed higher cleavage rate and blastocyst production than vitrified COCs group. Blastocysts were successfully obtained after IVF and ICSI procedures; however, the development to the blastocyst stage was better after IVF. These results show that the vitrification-warming media, the employment of a granulosa cell co-culture system and the Cryolock method during vitrification, increased the nuclear and cytoplasmic maturation of vitrified porcine immature oocytes. Further experiments are required to enhance porcine embryo production after vitrification.
本研究旨在评估玻璃化冷冻的猪未成熟卵母细胞在体外受精或卵胞浆内单精子注射情况下的成熟及受精能力,并确定随后的胚胎发育情况。未成熟卵母细胞采用乙二醇和二甲亚砜作为冷冻保护剂,运用Cryolock方法进行玻璃化冷冻。解冻后,卵母细胞培养44小时以使其成熟。将卵母细胞随机分为三个处理组,分别进行体外受精(实验1)或卵胞浆内单精子注射(实验2)操作。结果表明,与卵丘 - 卵母细胞复合体(COCs组)相比,经体外受精或卵胞浆内单精子注射受精后,与颗粒细胞共培养的裸卵(NkO - CC组)胚胎发育率更高,与对照组相比无显著差异。在NkO - CC共培养系统中成熟的玻璃化冷冻裸卵,其卵裂率和囊胚形成率高于玻璃化冷冻的COCs组。体外受精和卵胞浆内单精子注射操作后均成功获得了囊胚;然而,体外受精后发育至囊胚阶段的情况更好。这些结果表明,玻璃化冷冻 - 解冻培养基、颗粒细胞共培养系统的应用以及玻璃化冷冻过程中的Cryolock方法,提高了玻璃化冷冻猪未成熟卵母细胞的核成熟和胞质成熟。需要进一步实验以提高玻璃化冷冻后猪胚胎的产量。