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影响液滴玻璃化处理牛卵母细胞存活率的因素。

Factors affecting the survivability of bovine oocytes vitrified in droplets.

作者信息

Papis K, Shimizu M, Izaike Y

机构信息

lnstitute of Genetics and Animal Breeding, Jastrzebiec, Mroków, Poland.

出版信息

Theriogenology. 2000 Sep 15;54(5):651-8. doi: 10.1016/S0093-691X(00)00380-0.

Abstract

Vitrification of bovine oocytes performed using the traditional, in straw system has not given satisfactory results. Although an alternative approach based on minimizing the volume of the vitrified sample has recently resulted in a much more promising survival rate of vitrified oocytes, we attempted to examine some additional factors influencing the survival and subsequent fertilization and development rates of bovine oocytes subjected to vitrification according to the minimum drop size approach. In total, 748 bovine, in vitro matured oocytes were vitrified using VS14 vitrification solution, containing 5.5-M ethylene glycol and 1.0-M sucrose after different pre-equilibration and equilibration protocols performed at 35 degrees to 37 degrees C. Experiment 1 showed no significant toxic effect during pre-equilibration treatments of oocytes in 2%, 4% or 6% ethylene glycol solutions, except the lower cleavage rate of oocytes exposed to 6% ethylene glycol (77.2% vs. 93.9% in control, P< 0.05). In Experiment 2, 12 to 15 min of pre-equilibration treatments in 0%, 1% or 2% ethylene glycol solutions were tested, followed by 30 or 45 sec of equilibration in VS 14 solution and vitrification in droplets of medium dropped directly into liquid nitrogen. The development rate of vitrified oocytes to the blastocyst stage tended to be higher after 30-sec equilibration treatment (9.5%, 13.9% and 13.8% in groups of oocytes pre-equilibrated in 0%, 1% or 2% ethylene glycol solutions, respectively). Experiment 3 tested pre-equilibration treatments in 0%, 1%, 2%, 3%, 4%, 5% or 6% ethylene glycol solutions, followed by 30-sec equilibration and vitrification in droplets. The highest cleavage, blastocyst and hatched blastocyst rates, which were not significantly different from control, were achieved in a group of oocytes pre-equilibrated in 3% ethylene glycol solution (76%, 30% and 15% vs. 89%, 42% and 21% in control, respectively). A healthy calf was born on Feb 22 1999, after transfer of 4 morula/blastocyst stage embryos developed from oocytes vitrified in droplets after pre-equilibration in 3% ethylene glycol solution. We conclude that gentle pre-equilibration of bovine oocytes in diluted, 3% ethylene glycol solution is an important factor improving the effectiveness of vitrification in droplets of bovine oocytes.

摘要

使用传统的细管系统对牛卵母细胞进行玻璃化冷冻,尚未取得令人满意的结果。尽管最近一种基于最小化玻璃化样本体积的替代方法使玻璃化卵母细胞的存活率更具前景,但我们试图根据最小液滴法研究一些其他因素,这些因素会影响玻璃化处理后的牛卵母细胞的存活以及随后的受精和发育率。总共748个体外成熟的牛卵母细胞,在35℃至37℃下进行不同的预平衡和平衡方案后,使用含有5.5 M乙二醇和1.0 M蔗糖的VS14玻璃化溶液进行玻璃化冷冻。实验1表明,在2%、4%或6%乙二醇溶液中对卵母细胞进行预平衡处理期间,未观察到显著的毒性作用,但暴露于6%乙二醇的卵母细胞的分裂率较低(77.2%对对照组的93.9%,P<0.05)。在实验2中,测试了在0%、1%或2%乙二醇溶液中进行12至15分钟的预平衡处理,然后在VS14溶液中平衡30或45秒,并直接将培养基液滴滴入液氮中进行玻璃化冷冻。在平衡30秒的处理后,玻璃化卵母细胞发育到囊胚阶段的比率往往更高(在分别用0%、1%或2%乙二醇溶液预平衡的卵母细胞组中,比率分别为9.5%、13.9%和13.8%)。实验3测试了在0%、1%、2%、3%、4%、5%或6%乙二醇溶液中进行预平衡处理,然后平衡30秒并进行液滴玻璃化冷冻。在一组用3%乙二醇溶液预平衡的卵母细胞中,获得了最高的分裂、囊胚和孵化囊胚率,与对照组无显著差异(分别为76%、30%和15%对对照组的89%、42%和21%)。在将由在3%乙二醇溶液中预平衡后进行液滴玻璃化冷冻的卵母细胞发育而来的4个桑葚胚/囊胚阶段胚胎移植后,1999年2月22日出生了一头健康的小牛。我们得出结论,在稀释的3%乙二醇溶液中对牛卵母细胞进行温和的预平衡处理是提高牛卵母细胞液滴玻璃化冷冻效果的一个重要因素。

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