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表皮生长因子(EGF)和胰岛素样生长因子-I(IGF-I)联合使用可加速体外培养的牛卵泡卵母细胞减数分裂进程,而胎牛血清可中和这种加速作用。

A combination of EGF and IGF-I accelerates the progression of meiosis in bovine follicular oocytes in vitro and fetal calf serum neutralizes the acceleration effect.

作者信息

Sakaguchi M, Dominko T, Leibfried-Rutledge M L, Nagai T, First N L

机构信息

Laboratory of Animal Reproduction, Tohoku National Agricultural Experiment Station, Morioka, Iwate, Japan.

出版信息

Theriogenology. 2000 Nov 1;54(8):1327-42. doi: 10.1016/s0093-691x(00)00439-8.

Abstract

The effects of a combination of EGF and IGF-I (GFs) on the progress of meiosis and on their developmental competence were examined in cumulus-enclosed bovine oocytes. Exposure to GFs in serum-free, 0.3% PVP-containing maturation medium significantly (P<0.05) increased the frequency of oocytes with the first polar body (PB) at 16 h of culture and decreased those with PB at 20 h. The cleavage rates of PB-extruded oocytes after fertilization were not affected by treatment of GFs during maturation culture, and blastocyst yield was not improved by GFs treatment. Although replacement of PVP from GFs-containing medium with fatty acid-free BSA did not affect the timing of PB extrusion, replacement with 10% FCS neutralized the acceleration effects of GFs. Replacement for macromolecule in maturation medium did not improve blastocyst yield of PB-extruded oocytes after fertilization. These results indicate that the progression of meiosis in bovine oocytes with cumulus cells is accelerated by exposure to GFs in serum-free maturation medium but their developmental competence is not improved, and that the acceleration effects on the progress of meiosis is neutralized by the presence of FCS in maturation medium with no improvement of developmental competence after in vitro fertilization.

摘要

在卵丘包裹的牛卵母细胞中,研究了表皮生长因子(EGF)和胰岛素样生长因子-I(IGF-I,生长因子)的组合对减数分裂进程及其发育能力的影响。在无血清、含0.3%聚乙烯吡咯烷酮(PVP)的成熟培养基中暴露于生长因子,显著(P<0.05)提高了培养16小时时排出第一极体(PB)的卵母细胞频率,并降低了培养20小时时排出PB的卵母细胞频率。成熟培养期间生长因子处理不影响受精后排出PB的卵母细胞的分裂率,生长因子处理也未提高囊胚率。虽然用无脂肪酸牛血清白蛋白(BSA)替代含生长因子培养基中的PVP不影响PB排出时间,但用10%胎牛血清(FCS)替代可抵消生长因子的加速作用。替代成熟培养基中的大分子并未提高受精后排出PB的卵母细胞的囊胚率。这些结果表明,在无血清成熟培养基中暴露于生长因子可加速有卵丘细胞的牛卵母细胞减数分裂进程,但不提高其发育能力,并且成熟培养基中FCS的存在可抵消对减数分裂进程的加速作用,体外受精后发育能力未得到改善。

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