Rizos Dimitrios, Ward Fabian, Duffy Pat, Boland Maurice P, Lonergan Patrick
Department of Animal Science and Production and Conway Institute for Biomedical and Biomolecular Research, University College Dublin, Lyons Research Farm, Newcastle, County Dublin, Ireland.
Mol Reprod Dev. 2002 Feb;61(2):234-48. doi: 10.1002/mrd.1153.
The aim of this study is to examine the effect of bovine oocyte maturation, fertilization or culture in vivo or in vitro on the proportion of oocytes reaching the blastocyst stage, and on blastocyst quality as measured by survival following vitrification. In Experiment 1, 4 groups of oocytes were used: (1) immature oocytes from 2-6 mm follicles; (2) immature oocytes from > 6 mm follicles; (3) immature oocytes recovered in vivo just before the LH surge; and (4) in vivo matured oocytes. Significantly more blastocysts developed from oocytes matured in vivo than those recovered just before the LH surge or than oocytes from 2-6 mm follicles. Results from > 6 mm follicles were intermediate. All blastocysts had low survival following vitrification. In Experiment 2, in vivo matured oocytes were either (1) fertilized in vitro or (2) fertilized in vivo by artificial insemination and the resulting presumptive zygotes recovered on day 1. Both groups were then cultured in vitro. In vivo fertilized oocytes had a significantly higher blastocyst yield than those fertilized in vitro. Blastocyst quality was similar between the groups. Both groups had low survival following vitrification. In Experiment 3a, presumptive zygotes produced by in vitro maturation (IVM)/fertilization (IVF) were cultured either in vitro in synthetic oviduct fluid, or in vivo in the ewe oviduct. In Experiment 3b, in vivo matured/in vivo fertilized zygotes were either surgically recovered on day 1 and cultured in vitro in synthetic oviduct fluid, or were nonsurgically recovered on day 7. There was no difference in blastocyst yields between groups of zygotes originating from the same source (in vivo or in vitro fertilization) irrespective of whether culture took place in vivo or in vitro. However, there was a dramatic effect on blastocyst quality with those blastocysts produced following in vivo culture surviving vitrification at significantly higher rates than their in vitro cultured counterparts. Collectively, these results indicate that the intrinsic quality of the oocyte is the main factor affecting blastocyst yields, while the conditions of embryo culture have a crucial role in determining blastocyst quality.
本研究的目的是检测牛卵母细胞体内或体外成熟、受精或培养对发育至囊胚阶段的卵母细胞比例,以及对通过玻璃化冷冻后的存活率来衡量的囊胚质量的影响。在实验1中,使用了4组卵母细胞:(1)来自2 - 6毫米卵泡的未成熟卵母细胞;(2)来自大于6毫米卵泡的未成熟卵母细胞;(3)在促黄体生成素(LH)峰即将出现前体内回收的未成熟卵母细胞;(4)体内成熟的卵母细胞。与在LH峰即将出现前回收的卵母细胞或来自2 - 6毫米卵泡的卵母细胞相比,体内成熟的卵母细胞发育出的囊胚显著更多。来自大于6毫米卵泡的卵母细胞的结果处于中间水平。所有囊胚在玻璃化冷冻后的存活率都很低。在实验2中,将体内成熟的卵母细胞要么(1)进行体外受精,要么(2)通过人工授精进行体内受精,并在第1天回收所得的假定受精卵。然后将两组都进行体外培养。体内受精的卵母细胞的囊胚产量显著高于体外受精的卵母细胞。两组之间的囊胚质量相似。两组在玻璃化冷冻后的存活率都很低。在实验3a中,将体外成熟(IVM)/体外受精(IVF)产生的假定受精卵要么在合成输卵管液中进行体外培养,要么在母羊输卵管中进行体内培养。在实验3b中,将体内成熟/体内受精的受精卵要么在第1天通过手术回收并在合成输卵管液中进行体外培养,要么在第7天通过非手术回收。无论培养是在体内还是体外进行,来自相同来源(体内或体外受精)的受精卵组之间的囊胚产量没有差异。然而,对囊胚质量有显著影响,体内培养产生的囊胚在玻璃化冷冻后的存活率显著高于其体外培养的对应物。总体而言,这些结果表明卵母细胞的内在质量是影响囊胚产量的主要因素,而胚胎培养条件在决定囊胚质量方面起着关键作用。