Kono T, Tsunoda Y
National Institute of Animal Industry, Ibaraki, Japan.
Cryobiology. 1988 Jun;25(3):197-202. doi: 10.1016/0011-2240(88)90026-0.
The present study was conducted to compare the resistance of the nuclei with that of the cytoplasm of mouse zygotes to damage during the vitrification-warming cycle using the technique of pronuclear transplantation. Zygotes were collected from the oviduct of superovulated F1 female mice mated with males of the same strain. They were cryopreserved by the vitrification method. After being diluted with glycerol-sucrose PB1 solution, 86% of the recovered zygotes were morphologically normal and 80% of them developed to the two-cell stage in vitro, but the proportion of zygotes which developed to blastocysts was only 27%. When zygotes were exposed to VS1 solution in the same manner as above without cooling, 61% of them developed to blastocysts. In order to examine the source of injury during vitrification, the pronuclei of vitrified zygotes were transferred into enucleated fresh zygotes and vice versa. The developmental rate of blastocysts from vitrified zygotes that were enucleated and fused with pronuclei from fresh zygotes was significantly higher than that of zygotes reconstituted reversely. These findings suggest that nuclei are apparently damaged more than cytoplasm by the vitrification-warming cycle and the toxicity of VS1 solution.
本研究旨在利用原核移植技术,比较小鼠受精卵在玻璃化冷冻-复温过程中细胞核与细胞质对损伤的耐受性。从超排卵的F1雌性小鼠与同品系雄性小鼠交配后的输卵管中收集受精卵。采用玻璃化法对其进行冷冻保存。用甘油-蔗糖PB1溶液稀释后,86%的复苏受精卵形态正常,其中80%在体外发育至二细胞期,但发育至囊胚的受精卵比例仅为27%。当受精卵以与上述相同的方式暴露于VS1溶液而不进行冷却时,61%的受精卵发育至囊胚。为了研究玻璃化过程中的损伤来源,将玻璃化受精卵的原核转移到去核的新鲜受精卵中,反之亦然。去核的玻璃化受精卵与新鲜受精卵的原核融合后发育至囊胚的比率显著高于反向重构的受精卵。这些发现表明,在玻璃化冷冻-复温过程以及VS1溶液的毒性作用下,细胞核比细胞质明显更容易受到损伤。