Anas M K, Shojo A, Shimada M, Terada T
Graduate School for International Development and Cooperation, Hiroshima University, Higashi-Hiroshima.
Theriogenology. 2000 Jun;53(9):1797-806. doi: 10.1016/s0093-691x(00)00315-0.
The present study was conducted with the objective of examining the effect of wortmanin, a specific PI 3-kinase inhibitor, on the kinetic of GVBD, and on the activities of the maturation-promoting factor (MPF) and mitogen-activated protein (MAP) kinase during bovine oocyte maturation. The time sequence for GVBD was not different between oocytes cultured with or without wortmannin. Most of the cultured oocytes were at the filamentous bivalents stage after 4 h of culture. Six hours after the start of culture, most of the oocytes possessed germinal vesicles with condensed bivalent, and by 10 h of culture nearly all of the cultured oocytes underwent GVBD. A gradual increase in MPF activity until 12 h of culture was observed in the presence and absence of wortmannin. A sharp decrease in MPF activity in oocytes cultured without wortmannin treatment was recorded at 14 h of culture. Thereafter, MPF regained activity, reaching a maximum level at 20 to 24 h of culture. For oocytes cultured with wortmannin, no decline in the activity of MPF was observed during the interval from 12 to 24 h of culture. For these oocytes the MPF activity remained nearly stable during this transition until the end of incubation. The presence of wortmannin in the maturation medium did not alter MAP kinase activity. Taken together, these observations indicate that inhibition of PI 3-kinase does not modulate the time sequence of GVBD or the pattern of MAP kinase activity in bovine oocytes. However, PI 3-kinase might be one of the molecules that regulate the sharp reduction in the activity of MPF during the MI/MII transition.
本研究旨在检测特异性PI 3激酶抑制剂渥曼青霉素对牛卵母细胞成熟过程中GVBD动力学、成熟促进因子(MPF)活性和丝裂原活化蛋白(MAP)激酶活性的影响。在添加或不添加渥曼青霉素培养的卵母细胞中,GVBD的时间顺序没有差异。培养4小时后,大多数培养的卵母细胞处于丝状二价体阶段。培养开始6小时后,大多数卵母细胞的生发泡内含有浓缩的二价体,培养至10小时时,几乎所有培养的卵母细胞都发生了GVBD。在添加和不添加渥曼青霉素的情况下,均观察到培养至12小时时MPF活性逐渐增加。在未用渥曼青霉素处理的培养卵母细胞中,培养至14小时时记录到MPF活性急剧下降。此后,MPF活性恢复,在培养20至24小时时达到最高水平。对于用渥曼青霉素培养的卵母细胞,在培养12至24小时期间未观察到MPF活性下降。对于这些卵母细胞,在这个转变过程中MPF活性在整个孵育结束前几乎保持稳定。成熟培养基中渥曼青霉素的存在不会改变MAP激酶活性。综上所述,这些观察结果表明,PI 3激酶的抑制作用不会调节牛卵母细胞中GVBD的时间顺序或MAP激酶活性模式。然而,PI 3激酶可能是在MI/MII转变过程中调节MPF活性急剧下降的分子之一。