Barile V L, Dell'Aquila M E, Cinone M, Minoia P
Istituto di Biologia della Riproduzione ed Ostetricia degli Animali Domestici dell'Università di Bari.
Boll Soc Ital Biol Sper. 1990 Sep;66(9):899-906.
This work aims towards developing research concerning the improvement of animal reproduction, embryo development and genetic engineering. In our laboratory, an attempt has been made to standardize in vitro conditions able to optimally support bovine oocyte maturation and fertilization in order to yield viable embryos. Ovaries from cows and heifers, obtained from local slaughter-house, were used for recovery of oocytes from antral follicles. Cumulus-oocyte complexes were statically cultured for 24h at 39 degrees C in medium TCM 199 supplemented with fetal calf serum inactivated, hormones, glucose and granulosa cells under a 5% CO2 and 95% humidity atmosphere. A first group of oocytes was used for fixing and staining procedure for evidence of in vitro maturation. After culture 69.4% (77/111) of oocytes reached full maturation showing cumulus expansion, first polar body extrusion and the 2nd metaphase plate. A 2nd group was used for in vitro fertilization. In vitro semen capacitation was obtained with swim-up system (8.9) with separation of high motility fraction in Talp Hepes medium. Oocytes and spermatozoa were coincubated for 18-20h in Talp medium at 39 degrees C with 5% CO2 and 95% humidity. At the end of culture stereoscope and microscope observations were made for evidence of fertilization. After IVF 67.4% (58/86) resulted fertilized. Most of them showed two pronuclei and residual sperm tail. In few cases oocytes with 1 pronucleus and the swollen sperm head or with syngamy or polyspermic were found. In these experiments high percentages of in vitro matured and in vitro fertilized oocytes have been obtained. These bovine zygotes can be considered an essential step to develop new technologies in cattle breeding.
这项工作旨在开展有关改善动物繁殖、胚胎发育和基因工程的研究。在我们实验室,已尝试对体外条件进行标准化,以最佳支持牛卵母细胞成熟和受精,从而获得有活力的胚胎。从当地屠宰场获取的母牛和小母牛的卵巢,用于从窦状卵泡中回收卵母细胞。卵丘 - 卵母细胞复合体在补充有灭活胎牛血清、激素、葡萄糖和颗粒细胞的TCM 199培养基中,于39℃、5%二氧化碳和95%湿度的气氛下静态培养24小时。第一组卵母细胞用于固定和染色程序,以证明体外成熟情况。培养后,69.4%(77/111)的卵母细胞达到完全成熟,表现为卵丘扩展、第一极体排出和第二中期板。第二组用于体外受精。通过上浮系统(8.9)在Talp Hepes培养基中分离高活力部分,实现体外精液获能。卵母细胞和精子在Talp培养基中于39℃、5%二氧化碳和95%湿度下共同孵育18 - 20小时。培养结束时,通过实体显微镜和显微镜观察来证明受精情况。体外受精后,67.4%(58/86)的卵母细胞受精。其中大多数显示两个原核和残留的精子尾部。在少数情况下,发现有1个原核且精子头部肿胀或发生了受精或多精受精的卵母细胞。在这些实验中,获得了高比例的体外成熟和体外受精的卵母细胞。这些牛受精卵可被视为牛育种新技术发展的关键一步。