Shirazi A, Ostad-Hosseini S, Ahmadi E, Heidari B, Shams-Esfandabadi N
Research Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran.
Theriogenology. 2009 Jan 15;71(2):342-8. doi: 10.1016/j.theriogenology.2008.07.027. Epub 2008 Aug 31.
The present study was conducted to determine the necessity for activation after intracytoplasmic sperm injection (ICSI) in sheep. The effect of chemical stimulation with either 5microM ionomycin (I) for 5min or ionomycin+2mM 6-dimethylaminopurine (6-DMAP) for 3h on the efficiency of ICSI, was compared in six experimental groups: (1) ICSI, (2) ICSI+I, (3) ICSI+I+6DMAP, (4) Sham, (5) Sham+I, and (6) parthenogenetics (Sham and parthenogenetic groups were used as controls). In the present study, ovine oocytes needed additional chemical stimulation, after conventional ICSI, to activate (female pronucleous formation) and to form zygotes with male and female pronuclei (2PN). The percentage of cleaved embryos obtained and developed to blastocyst stage was higher (P<0.001) for ICSI-derived zygotes, followed by activation (I and I+6DMAP; 18.2 and 22.5%, respectively) than ICSI and Sham injection without activation (3.0 and 0.0%, respectively). There was, however, no significant difference between activation protocols I or I+6DMAP. Furthermore, there was no significant difference among chemically activated, ICSI-derived zygotes in term of hatchability rate; however, the percentage was significantly higher in parthenogenetic and IVF groups than ICSI and Sham injection. In conclusion, neither sperm alone nor mechanical activation was sufficient for ovine oocyte activation and pronuclei formation. Therefore, in our study conditions for in vitro embryo development, chemical activation of oocytes must be considered an essential part of the ICSI procedure in sheep.
本研究旨在确定绵羊卵胞浆内单精子注射(ICSI)后激活的必要性。在六个实验组中比较了用5微摩尔离子霉素(I)处理5分钟或离子霉素+2毫摩尔6-二甲基氨基嘌呤(6-DMAP)处理3小时的化学刺激对ICSI效率的影响:(1)ICSI组,(2)ICSI+I组,(3)ICSI+I+6DMAP组,(4)假注射组,(5)假注射+I组,以及(6)孤雌生殖组(假注射组和孤雌生殖组用作对照)。在本研究中,绵羊卵母细胞在常规ICSI后需要额外的化学刺激来激活(形成雌原核)并形成具有雄原核和雌原核的合子(双原核,2PN)。与未激活的ICSI和假注射组(分别为3.0%和0.0%)相比,ICSI来源的合子经激活(I和I+6DMAP;分别为18.2%和22.5%)后获得的分裂胚胎百分比和发育到囊胚阶段的百分比更高(P<0.001)。然而,激活方案I或I+6DMAP之间没有显著差异。此外,化学激活的ICSI来源的合子在孵化率方面没有显著差异;然而,孤雌生殖组和体外受精组的百分比显著高于ICSI组和假注射组。总之,单独的精子或机械激活都不足以激活绵羊卵母细胞并形成原核。因此,在我们的体外胚胎发育研究条件下,卵母细胞的化学激活必须被视为绵羊ICSI程序的一个重要部分。