Tsunoda Y, Yasui T, Nakamura K, Uchida T, Sugie T
J Exp Zool. 1986 Oct;240(1):119-25. doi: 10.1002/jez.1402400115.
A new and reliable pronuclear transplantation procedure for the mouse egg has been developed by McGrath and Solter ('83). To overcome the technical difficulties of such a procedure, especially in uniformly preparing enucleation pipettes and in reducing damages during micromanipulation, we have examined the effect of cutting the zona pellucida of the eggs. By making a slit in the zona of an egg, the time for pipetting and exchange of pronuclei between eggs was shortened because the sharp tip of the pipette was not necessary. Although the proportion of pregnant recipients and young obtained after transfer of pronuclear transplanted eggs cultured for 1 day or 3 days was quite low, it was significantly increased (70% for pregnancy rate and 32% for the young) following transfer of eggs cultured for 4 days. These values were comparable with those after transfer of unoperated eggs cultured to morulae and blastocysts.
麦克格拉斯和索尔特(1983年)开发了一种用于小鼠卵子的新型可靠的原核移植程序。为了克服该程序的技术难题,尤其是在统一制备去核吸管以及减少显微操作过程中的损伤方面,我们研究了切割卵子透明带的效果。通过在卵子的透明带上切一个小口,移液以及卵子间原核交换的时间得以缩短,因为不再需要吸管的尖锐尖端。尽管移植培养1天或3天的原核移植卵子后怀孕受体和幼崽的比例相当低,但在移植培养4天的卵子后,这一比例显著提高(妊娠率为70%,幼崽率为32%)。这些数值与移植培养至桑葚胚和囊胚阶段的未操作卵子后的数值相当。