利用青春期前雄性小鼠的第一波精子进行体外受精的早期后代生产

K. Mochida, A. Hasegawa, N. Ogonuki, K. Inoue, A. Ogura
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引用次数: 5

摘要

成熟雄性小鼠(10-12周或更大)通常用于体外受精(IVF),以获得高受精率(例如,> 70%)。在这里,我们试图确定雄性小鼠(C57BL/6J品系)可以有效地通过体外受精产生后代的最早年龄。因为我们注意到,在试管婴儿培养基中添加还原型谷胱甘肽(GSH)可以显著提高青春期前男性精子的受精能力,所以我们在所有实验中都使用了这种试管婴儿方案。精子在第35天首先到达附睾尾部区域;然而,它们不能使卵母细胞受精。尾侧附睾精子在第37天首先具有与卵母细胞受精的能力,尽管率很低(2.9%)。第40天受精率为72.0%,移植后成虫率为52.4%。此外,我们还发现,青春期前小鼠附睾精子可以使卵母细胞受精;但无论雄虫年龄大小,受精率均< 50%。不论雄鼠年龄大小,附睾头精子均不能使卵母细胞受精。因此,我们建议40日龄雄性小鼠的尾侧附睾精子可以有效地用于体外受精,在最短的时间内获得后代。与传统的体外受精方案相比,该方案将减少小鼠生成所需的周转时间约1个月。
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Early production of offspring by in vitro fertilization using first-wave spermatozoa from prepubertal male mice
Mature male mice (aged 10–12 weeks or older) are conventionally used for in vitro fertilization (IVF) in order to achieve high fertilization rates (e.g., > 70%). Here, we sought to determine the earliest age at which male mice (C57BL/6J strain) can be used efficiently for producing offspring via IVF. Because we noted that the addition of reduced glutathione (GSH) to the IVF medium significantly increased the fertilizing ability of spermatozoa from prepubertal males, we used this IVF protocol for all experiments. Spermatozoa first reached the caudal region of the epididymides at day 35; however, they were unable to fertilize oocytes. Caudal epididymal spermatozoa first became competent for oocyte fertilization at day 37, albeit at a low rate (2.9%). A high fertilization rate (72.0%) was obtained at day 40, and 52.4% of the embryos thus obtained developed into offspring after embryo transfer. Moreover, we found that corpus epididymal spermatozoa in prepubertal mice could fertilize oocytes; however, the fertilization rates were always < 50%, regardless of the age of the males. Caput epididymal spermatozoa failed to fertilize oocytes irrespective of the age of the males. Therefore, we propose that caudal epididymal spermatozoa from male mice aged 40 days can be efficiently used for IVF, to obtain offspring in the shortest attainable time. This protocol will reduce the turnover time required for the generation of mice by ~1 month compared with that of the conventional IVF protocol.
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