Wehrend A, Meinecke B
Clinic for Obstetrics, Gynaecology and Andrology of Large and Small Animals, Justus-Liebig-University, Frankfurter Str. 106, D-35392, Giessen, Germany.
Anim Reprod Sci. 2001 May 31;66(3-4):175-84. doi: 10.1016/s0378-4320(01)00094-x.
The kinetics of nuclear maturation, M-phase promoting factor (MPF) and mitogen-activated protein kinase (MAP kinase) activities during in vitro maturation of porcine and bovine oocytes were examined. A further objective was to determine the duration of the meiotic stages during the maturation process. Porcine and bovine cumulus-oocyte complexes (COCs) were incubated in TCM 199 supplemented with 20% (v/v) heat inactivated fetal calf serum (FCS), 0.05microg/ml gentamycin, 0.02mg/ml insulin, 2.5microg/ml FSH and 5microg/ml LH. COCs were removed from the culture media in hourly intervals starting immediately after recovery from the follicle until 24 (bovine) or 48h (porcine) of culture. Oocytes were either fixed to evaluate the maturation status or the activity of MPF, assessed by its histone H1 kinase activity, and MAP kinase were determined by a radioactive assay simultaneously. In oocytes of both species, the MPF activity oscillated during the culture period with two maxima corresponding with the two metaphases: between 27-32 and after 46h (porcine) and between 6-9 and after 22h (bovine). There was a temporary decline in activity after 33-38 (porcine) and after 19h (bovine), which corresponded with anaphase I and telophase I. MAP kinase activity increased during the whole culture period and reached maximum levels after 47 (porcine) and after 22h (bovine). In porcine oocytes, the MAP kinase was activated before GVBD and MPF activation. In bovine oocytes, MPF and MAP kinase were activated at approximately the same time as the GVBD (8-9h of incubation). In average porcine, oocytes remain 23.4h in the germinal vesicle (GV) stage (13h in GV I, 5.7h in GV II, 3.2h in GV III and 1.5h in GV IV), 0.9h in diakinese, 9.6h in the metaphase I, 2.8h in anaphase I and 1.9h in telophase I of the first meiotic division. In bovine oocytes, the temporal distribution of the meiotic stages were 8.5h for the GV stage, 1.2h for diakinese, 8.3h for metaphase I, 1.6h for anaphase I and 1.9h for telophase I. These results indicate that the duration of the meiotic stages differs between the species and that MAP kinase is activated before MPF and GVBD in porcine oocytes.
研究了猪和牛卵母细胞体外成熟过程中核成熟动力学、M期促进因子(MPF)和丝裂原活化蛋白激酶(MAP激酶)的活性。另一个目标是确定成熟过程中减数分裂各阶段的持续时间。将猪和牛的卵丘-卵母细胞复合体(COCs)培养于补充有20%(v/v)热灭活胎牛血清(FCS)、0.05μg/ml庆大霉素、0.02mg/ml胰岛素、2.5μg/ml促卵泡素(FSH)和5μg/ml促黄体素(LH)的TCM 199中。从卵泡中取出后立即开始,每隔一小时从培养基中取出COCs,直至培养24小时(牛)或48小时(猪)。卵母细胞要么固定以评估成熟状态,要么通过其组蛋白H1激酶活性评估MPF的活性,同时通过放射性测定法测定MAP激酶。在两个物种的卵母细胞中,MPF活性在培养期间振荡,有两个最大值,分别对应两个中期:猪在27 - 32小时之间以及46小时后,牛在6 - 9小时之间以及22小时后。在33 - 38小时(猪)和19小时(牛)后活性出现暂时下降,这与减数第一次分裂后期和末期相对应。MAP激酶活性在整个培养期间增加,并在47小时(猪)和22小时(牛)后达到最高水平。在猪卵母细胞中,MAP激酶在生发泡破裂(GVBD)和MPF激活之前被激活。在牛卵母细胞中,MPF和MAP激酶与GVBD(培养8 - 9小时)大致同时被激活。猪卵母细胞平均在生发泡(GV)期停留23.4小时(GV I期13小时、GV II期5.7小时、GV III期3.2小时、GV IV期1.5小时),在终变期停留0.9小时,在减数第一次分裂中期停留9.6小时,在后期停留2.8小时,在末期停留1.9小时。牛卵母细胞减数分裂各阶段的时间分布为:GV期8.5小时、终变期1.2小时、中期I 8.3小时、后期I 1.6小时、末期I 1.9小时。这些结果表明,减数分裂各阶段的持续时间在不同物种之间存在差异,并且在猪卵母细胞中MAP激酶在MPF和GVBD之前被激活。