Drakakis P, Loutradis D, Milingos S, Bletsa R, Kallianidis K, Michalas S, Aravantinos D
Alexandra Maternity Hospital, 1st Department of Ob/Gyn, Athens University Medical School, Greece.
J Assist Reprod Genet. 1996 Nov;13(10):786-92. doi: 10.1007/BF02066499.
The purpose of this study was to investigate the effect of male and female serum supplementation on the in vitro development of mouse embryos beyond the blastocyst stage until the outgrowth stage since the latter may be related to the nidation of the embryo. We also studied the effect of EGF addition on embryo culture and blastocyst outgrowth.
The blastocyst and hatching rates of two-cell mouse embryos cultured in Ham's F-10 + BSA, Ham's F-10 + male serum, or Ham's F-10 + female serum were found to be comparable (P > 0.05). The outgrowth rate of hatched blastocysts was significantly increased, though, when they were transferred to 50% male serum compared to either 50% BSA or 50% female serum (P < 0.01 and P < 0.05, respectively). In the last experiment, either 100 or 150 ng/ml EGF was added to the culture medium from the two-cell stage till blastocyst development and the latter were cultured till outgrowth in 50% BSA, male serum, or female serum. For both concentrations of EGF, the outgrowth rate was significantly higher in male serum compared to the other conditions (P < 0.01 and P < 0.05, respectively). The outgrowth rate was also higher when EGF was used compared to plain medium before transferring the blastocysts to either male or female serum (P < 0.01 for both).
We conclude that the development of embryos to the outgrowth stage is significantly enhanced by male serum. The addition of EGF from the two-cell stage also significantly improves the outgrowth success rate for both male and female serum conditions.
本研究旨在探讨补充雄性和雌性血清对小鼠胚胎体外发育的影响,观察其从囊胚期发育至胚泡植入前的生长阶段,因为后者可能与胚胎着床有关。我们还研究了添加表皮生长因子(EGF)对胚胎培养和囊胚生长的影响。
我们发现,在Ham's F-10 + 牛血清白蛋白(BSA)、Ham's F-10 + 雄性血清或Ham's F-10 + 雌性血清中培养的双细胞小鼠胚胎,其囊胚形成率和孵化率相当(P > 0.05)。然而,与50% BSA或50%雌性血清相比,将孵化后的囊胚转移至50%雄性血清中时,胚泡生长率显著提高(分别为P < 0.01和P < 0.05)。在最后一项实验中,从双细胞期开始直至囊胚发育阶段,向培养基中添加100或150 ng/ml的EGF,并将囊胚在50% BSA、雄性血清或雌性血清中培养至生长阶段。对于两种浓度的EGF,雄性血清中的胚泡生长率均显著高于其他条件(分别为P < 0.01和P < 0.05)。在将囊胚转移至雄性或雌性血清之前,使用EGF时的胚泡生长率也高于普通培养基(两者均为P < 0.01)。
我们得出结论,雄性血清可显著促进胚胎发育至生长阶段。从双细胞期开始添加EGF也显著提高了雄性和雌性血清条件下的胚泡生长成功率。