不同活化处理对马卵母细胞胞浆内单精子注射受精的影响。

Xihe Li, L. Morris, W. Allen
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引用次数: 53

摘要

研究了四种试剂对马卵母细胞的激活和受精的影响,以及在卵浆内单精子注射后卵母细胞的发育。从屠宰场的马卵巢中收集卵母细胞复合物,在TCM199培养基中体外成熟40-44小时,然后在II中期注射固定的种马精子。然后对卵母细胞复合物进行五种激活处理之一:(a) 10微摩尔离子霉素1(-1)10分钟;(b) 7% (v/v)乙醇浸泡10 min;(c) 100微摩尔硫柳汞1(-1)浸泡10分钟;(d) 250微摩尔肌醇1,4,5 -三磷酸1(-1)注射液;(e)没有治疗(对照)。进一步培养18-20 h后,通过观察卵丘-卵母细胞复合物是否进入第二后期和末期并形成雌性原核来评估其活化情况。每次处理后激活的卵母细胞比例为:离子霉素组16/27 (59%);乙醇为14/25 (56%);硫柳汞22/28 (79%);1,4,5-三磷酸肌醇为15/27 (56%);未处理对照组为0/20(0%)。因此,硫柳汞处理的卵母细胞活化率显著高于其他4种处理(P < 0.05)。离子霉素组、乙醇组和硫柳汞组的卵母细胞在注射精子后24 ~ 30 h的卵母细胞分裂至双细胞期的比例分别为7/20(35%)、5/19(26%)和11/23(48%)。对照卵母细胞和经肌醇1,4,5 -三磷酸处理的卵母细胞均未见卵裂。此外,经离子霉素、乙醇和硫柳汞处理的卵母细胞中,有2/7(29%)、2/5(40%)和7/11(64%)的卵母细胞受精正常。这些结果表明:(a)离子霉素、乙醇、硫柳汞和肌醇(1,4,5-三磷酸)等化学刺激物可以激活马卵母细胞;(b)硫柳汞在促进马卵母细胞减数分裂激活和正常受精方面比其他三种试剂更有效;(c)化学激活也可能刺激卵母细胞的孤雌生殖分裂,而精子头部没有同时发生变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of different activation treatments on fertilization of horse oocytes by intracytoplasmic sperm injection.
The effects of four reagents on the activation and subsequent fertilization of equine oocytes, and the development of these after intracytoplasmic sperm injection, were investigated. Cumulus-oocyte complexes collected from equine ovaries obtained from an abattoir were matured in vitro for 40-44 h in TCM199 medium before being injected, when in metaphase II, with an immobilized stallion spermatozoon. The cumulus-oocyte complexes were then subjected to one of five activation treatments: (a) 10 micromol ionomycin l(-1) for 10 min; (b) 7% (v/v) ethanol for 10 min; (c) 100 micromol thimerosal l(-1) for 10 min; (d) 250 micromol inositol 1,4, 5-triphosphate l(-1) injection; and (e) no treatment (control). After 18-20 h further culture, the cumulus-oocyte complexes were assessed for activation by observing whether they had progressed through second anaphase-telophase and had formed a female pronucleus. The proportions of oocytes activated after each treatment were: 16/27 (59%) for ionomycin; 14/25 (56%) for ethanol; 22/28 (79%) for thimerosal; 15/27 (56%) for inositol 1,4,5-triphosphate; and 0/20 (0%) for the untreated controls. Thus, significantly more oocytes (P < 0.05) were activated by treatment with thimerosal than by the other four treatments. The proportions of oocytes that cleaved to the two-cell stage at 24-30 h after sperm injection in the groups treated with ionomycin, ethanol and thimerosal were 7/20 (35%), 5/19 (26%) and 11/23 (48%), respectively. No cleavage was observed in any of the control oocytes or those treated with inositol 1,4, 5-triphosphate. Furthermore, evidence of normal fertilization was observed in 2/7 (29%), 2/5 (40%) and 7/11 (64%) of the oocytes treated with ionomycin, ethanol and thimerosal, respectively. These results demonstrated that: (a) it is possible to activate equine oocytes with the chemical stimulants, ionomycin, ethanol, thimerosal and inositol 1,4,5-triphosphate; (b) thimerosal is more effective than the other three reagents in facilitating both meiotic activation and normal fertilization of equine oocytes; and (c) chemical activation may also stimulate parthenogenetic cleavage of oocytes without concurrent changes in the head of the spermatozoon.
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