Albarracín José Luis, Morató Roser, Izquierdo Dolors, Mogas Teresa
Departament de Medicina i Cirurgia Animals, Facultat de Veterinària, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.
Theriogenology. 2005 Nov;64(8):1740-55. doi: 10.1016/j.theriogenology.2005.04.018. Epub 2005 Jun 4.
Roscovitine, a potent inhibitor of M-phase promoting factor kinase activity, was used to maintain calf oocytes at the germinal vesicle stage for a 24h culture period. Cumulus-oocyte complexes were first prematured for 24h in the presence of different levels of roscovitine (12.5, 25, 50 and 100 microM). Roscovitine was shown to block germinal vesicle breakdown in calf oocytes in a concentration dependent manner. Significantly greater inhibitory effect was observed at 50 and 100 microM with 64.6% and 63.2% oocytes being blocked in the germinal vesicle stage when compared to the control (0.0%) and the 12.5 microM (2.9%) and 25 microM (18.8%) groups. However, this inhibitory effect of roscovitine was fully reversible since a substantial number of the oocytes resumed meiosis and reached the metaphase II stage after a further 24h of culture in a permissive medium. Cleavage rates and blastocyst yields were not significantly different for oocytes cultured under 50 microM roscovitine inhibition compared to oocytes not subjected to prematuration culture (rates of 76.7% cleavage and 8.7% blastocysts for control oocytes compared to 69.8% and 6.3%, respectively, for oocytes pretreated with 50 microM roscovitine). The morphology of the meiotic spindle was typical of metaphase II in 75.8% and 82.1% of the oocytes reaching the metaphase II stage after pretreatment with 50 microM roscovitine compared to control, respectively. A normal distribution of actin filaments was observed in 97.0% and 98.2% of oocytes exposed to 50 microM roscovitine compared to control, respectively. These results demonstrate the feasibility of maintaining calf oocytes in artificial meiotic arrest without compromising their subsequent developmental competence.
Roscovitine是一种有效的M期促进因子激酶活性抑制剂,用于在24小时培养期内将犊牛卵母细胞维持在生发泡期。卵丘-卵母细胞复合体首先在不同浓度(12.5、25、50和100微摩尔)的Roscovitine存在下进行24小时的早熟培养。结果表明,Roscovitine以浓度依赖的方式阻断犊牛卵母细胞的生发泡破裂。在50和100微摩尔浓度下观察到显著更强的抑制作用,与对照组(0.0%)、12.5微摩尔组(2.9%)和25微摩尔组(18.8%)相比,分别有64.6%和63.2%的卵母细胞被阻断在生发泡期。然而,Roscovitine的这种抑制作用是完全可逆的,因为在允许的培养基中再培养24小时后,大量卵母细胞恢复减数分裂并达到中期II阶段。与未进行早熟培养的卵母细胞相比,在50微摩尔Roscovitine抑制下培养的卵母细胞的分裂率和囊胚率没有显著差异(对照组卵母细胞的分裂率为76.7%,囊胚率为8.7%,而用50微摩尔Roscovitine预处理的卵母细胞的分裂率和囊胚率分别为69.8%和6.3%)。在用50微摩尔Roscovitine预处理后达到中期II阶段的卵母细胞中,分别有75.8%和82.1%的卵母细胞的减数分裂纺锤体形态典型,与对照组相比。与对照组相比,分别有97.0%和98.2%暴露于50微摩尔Roscovitine的卵母细胞观察到肌动蛋白丝的正常分布。这些结果证明了在不损害其随后发育能力的情况下将犊牛卵母细胞维持在人工减数分裂阻滞状态的可行性。