Reproductive Medical Center, Jilin Medical University, Jilin 132013, PR China.
Center for Reproductive Medicine, Wuxi Maternity and Child Health Care Hospital Affiliated to Nanjing Medical University, Wuxi 214002, PR China.
Clin Chim Acta. 2018 Oct;485:119-125. doi: 10.1016/j.cca.2018.06.041. Epub 2018 Jun 27.
In order to investigate the effects and mechanism of Bisphenol A (BPA) on the growth of preantral follicles and the maturation of oocytes in vitro, preantral follicles were harvested from mouse ovaries and in vitro cultured for 11 days with different concentrations of BPA (0, 4.5 and 45 μM) for calculating the percentages of antral follicles, denuded oocytes, degenerative oocytes and the maturation rate of oocytes, besides measuring the diameter of follicles and the thickness of cumulus cell layers.
The contents of estradiol (E) in the culture media on Day 4, 8 and 10 were detected by ELISA. The estrogen receptor (ER) expression, spindle morphology and chromosome distribution in oocytes on Day 10 and 11 were observed by immunofluorescence. Western blotting was used to detect the expressions of growth differentiation factor 9 (GDF-9), bone morphogenetic protein-15 (BMP-15), phosphorylated extracellular signal-regulated kinase 1 (p-Erk1) and phosphorylated Ca/calmodulin-dependent protein kinase II (p-CaMKII) in the oocytes.
Compared with control, BPA (45 μM) significantly reduced percentages of antral follicles (9.25% vs. 91.17%, P < 0.05) and the maturation rate of oocytes (7.61% vs. 79.83%, P < 0.05), but increased the percentages of denuded oocytes (30.29% vs. 3.36%, P < 0.05) and degenerative oocytes (45.70% vs. 2.45%, P < 0.05). The diameter of follicles and the thickness of the cumulus cell layers were decreased significantly (P < 0.05). Moreover, BPA (45 μM) significantly decreased E contents in the culture medium on Day 8 and 10 (P < 0.05) and the expressions of ER, GDF-9 and BMP-15 in oocytes (P < 0.05). Furthermore, BPA (4.5 and 45 μM) treatment resulted in the abnormal spindle morphology and chromosome distribution, and the decreased expressions of p-Erk1 and p-CaMKII in the MII oocytes.
Together, these results clearly demonstrated BPA retarded the preantral follicle growth in vitro through interfering with the synthesis and secretion of E and reducing the expressions of ER, GDF-9 and BMP-15, and led to the abnormal meioses of oocytes through reducing p-Erk1 and p-CaMKII expressions in the preantral follicles, which will help us to further unsderstand the mechanism of BPA exposure retarding in vitro growth of preantral follicles and maturation of oocyes.
为了研究双酚 A(BPA)对体外小鼠原始卵泡生长和卵母细胞成熟的影响及其作用机制,我们从小鼠卵巢中采集原始卵泡,并在含有不同浓度 BPA(0、4.5 和 45μM)的培养基中进行体外培养 11 天,计算腔前卵泡、去卵丘卵母细胞、退化卵母细胞的比例和卵母细胞的成熟率,同时测量卵泡直径和卵丘细胞层的厚度。
采用 ELISA 法检测第 4、8 和 10 天培养基中雌二醇(E)的含量。采用免疫荧光法观察第 10 和 11 天卵母细胞中雌激素受体(ER)的表达、纺锤体形态和染色体分布。采用 Western blot 法检测卵母细胞中生长分化因子 9(GDF-9)、骨形态发生蛋白 15(BMP-15)、磷酸化细胞外信号调节激酶 1(p-Erk1)和磷酸化钙/钙调蛋白依赖性蛋白激酶 II(p-CaMKII)的表达。
与对照组相比,BPA(45μM)显著降低了腔前卵泡的比例(9.25% vs. 91.17%,P<0.05)和卵母细胞的成熟率(7.61% vs. 79.83%,P<0.05),但增加了去卵丘卵母细胞的比例(30.29% vs. 3.36%,P<0.05)和退化卵母细胞的比例(45.70% vs. 2.45%,P<0.05)。卵泡直径和卵丘细胞层的厚度显著减小(P<0.05)。此外,BPA(45μM)显著降低了第 8 和 10 天培养基中 E 的含量(P<0.05)和卵母细胞中 ER、GDF-9 和 BMP-15 的表达(P<0.05)。此外,BPA(4.5 和 45μM)处理导致纺锤体形态和染色体分布异常,并降低了 MII 期卵母细胞中 p-Erk1 和 p-CaMKII 的表达。
综上所述,这些结果清楚地表明,BPA 通过干扰 E 的合成和分泌以及降低 ER、GDF-9 和 BMP-15 的表达,阻碍了体外原始卵泡的生长,并通过降低原始卵泡中 p-Erk1 和 p-CaMKII 的表达,导致卵母细胞减数分裂异常,这将有助于我们进一步了解 BPA 暴露阻碍体外原始卵泡生长和卵母细胞成熟的机制。