Fouladi Nashta A A, Waddington D, Campbell K H
Roslin Institute, Roslin, Midlothian EH25 9PS, Scotland, United Kingdom.
Biol Reprod. 1998 Aug;59(2):255-62. doi: 10.1095/biolreprod59.2.255.
The frequency of development of bovine embryos produced by maturation, fertilization, and culture in vitro is lower than that observed in vivo. One factor that may affect both the frequency of development and the quality of the embryos produced is the developmental competence of the oocyte. In current in vitro production systems, oocyte maturation, characterized by the resumption of meiosis, occurs after oocyte aspiration from the follicle. The developmental competence of individual oocytes may be improved by inducing maturation after culturing under conditions that inhibit the resumption of meiosis. In order to test this hypothesis, a system has been established in which intact antral follicles (3-8 mm in diameter) are cultured in vitro. During this period the oocytes are maintained at the germinal vesicle (GV) stage under the inhibitory effects of the follicle. Culture of intact antral follicles was compared with two other "physiological" methods for the maintenance of GV arrest: oocytes were cultured attached to a small part of the follicle wall or within hemisections of follicles. It was found that 96.8% of oocytes recovered from intact antral follicles-as compared to 24.6% attached to a small part of the follicle wall and 62.7% within hemisections of follicles-were maintained at the GV stage after 24-h culture. The effects on GV arrest and subsequent maturation of the oocytes were evaluated after longer periods of antral follicle culture (2, 4, and 7 days). As the culture period increased, the number of GV-arrested oocytes decreased; the maximum percentage of GV arrest was observed after 24-h culture. The majority of these oocytes matured to metaphase II. A comparison of blastocyst production was made after fertilization and subsequent development of oocytes obtained following follicle culture and of control oocytes aspirated directly from antral follicles. The cleavage rate and percentage of blastocyst production in these two groups were 54.6 +/- 13.9%, 48.4 +/- 8.4% and 68.6 +/- 8.6%, 32.8 +/- 10.8%, respectively. Statistical analysis showed significant differences in both cleavage rate and blastocyst production between these two groups. Total cell numbers in the control group were 144.6 +/- 7.28 and 152.0 +/- 25.8 after follicle culture. It is concluded that culture of intact antral follicles for 24 h is an alternative method for the maintenance of bovine oocytes in meiotic arrest and that these oocytes acquire a greater developmental competence in vitro.
通过体外成熟、受精和培养产生的牛胚胎发育频率低于体内观察到的频率。可能影响发育频率和所产生胚胎质量的一个因素是卵母细胞的发育能力。在当前的体外生产系统中,以减数分裂恢复为特征的卵母细胞成熟发生在从卵泡中吸出卵母细胞之后。在抑制减数分裂恢复的条件下培养后诱导成熟,可能会提高单个卵母细胞的发育能力。为了验证这一假设,建立了一个体外培养完整有腔卵泡(直径3 - 8毫米)的系统。在此期间,卵母细胞在卵泡的抑制作用下维持在生发泡(GV)期。将完整有腔卵泡的培养与另外两种维持GV期阻滞的“生理性”方法进行比较:将卵母细胞附着在一小部分卵泡壁上进行培养,或将卵母细胞培养在卵泡的半切片中。结果发现,从完整有腔卵泡中回收的卵母细胞,在培养24小时后,96.8%维持在GV期,而附着在一小部分卵泡壁上培养的卵母细胞为24.6%,在卵泡半切片中培养的卵母细胞为62.7%。在更长时间的有腔卵泡培养(2、4和7天)后,评估了对卵母细胞GV期阻滞和随后成熟的影响。随着培养时间的增加,处于GV期阻滞的卵母细胞数量减少;在培养24小时后观察到GV期阻滞的最大百分比。这些卵母细胞中的大多数成熟到中期II。对卵泡培养后获得的卵母细胞以及直接从有腔卵泡中吸出的对照卵母细胞进行受精和随后发育后,比较了囊胚的产生情况。这两组的卵裂率和囊胚产生百分比分别为54.6±13.9%、48.4±8.4%和68.6±8.6%、32.8±10.8%。统计分析表明,这两组在卵裂率和囊胚产生方面均存在显著差异。卵泡培养后对照组的总细胞数分别为144.6±7.28和152.0±25.8。结论是,将完整有腔卵泡培养24小时是维持牛卵母细胞减数分裂阻滞的一种替代方法,并且这些卵母细胞在体外获得了更高的发育能力。