Yan Zheng, Liang Hongxing, Deng Li, Long Hui, Chen Hong, Chai Weiran, Suo Lun, Xu Chen, Kuang Yanping, Wu Lingqian, Lu Shengsheng, Lyu Qifeng
Department of Assisted Reproduction, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200011, PR China.
Guangxi High Education key Laboratory for Animal Reproduction and Biotechnology, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi University, Nanning, 530004, PR China.
PLoS One. 2015 Dec 17;10(12):e0145172. doi: 10.1371/journal.pone.0145172. eCollection 2015.
Increased risk of monozygotic twinning (MZT) has been shown to be associated with assisted reproduction techniques, particularly blastocyst culture. Interestingly, inner cell mass (ICM) splitting in human '8'-shaped hatching blastocysts that resulted in MZT was reported. However, the underlying cause of MZT is not known. In this study, we investigated in a mouse model whether in vitro culture leads to ICM splitting and its association with hatching types. Blastocyst hatching was observed in: (i) in vivo developed blastocysts and (ii-iii) in vitro cultured blastocysts following in vivo or in vitro fertilization. We found that '8'-shaped hatching occurred with significantly higher frequency in the two groups of in vitro cultured blastocysts than in the group of in vivo developed blastocysts (24.4% and 20.4% versus 0.8%, respectively; n = 805, P < 0.01). Moreover, Oct4 immunofluorescence staining was performed to identify the ICM in the hatching and hatched blastocysts. Scattered and split distribution of ICM cells was observed around the small zona opening of '8'-shaped hatching blastocysts. This occurred at a high frequency in the in vitro cultured groups. Furthermore, we found more double OCT4-positive masses, suggestive of increased ICM splitting in '8'-shaped hatching and hatched blastocysts than in 'U'-shaped hatching and hatched blastocysts (12.5% versus 1.9%, respectively; n = 838, P < 0.01). Therefore, our results demonstrate that extended in vitro culture can cause high frequencies of '8'-shaped hatching, and '8'-shaped hatching that may disturb ICM herniation leading to increased risk of ICM splitting in mouse blastocysts. These results may provide insights into the increased risk of human MZT after in vitro fertilization and blastocyst transfer.
单卵双胎(MZT)风险增加已被证明与辅助生殖技术有关,尤其是囊胚培养。有趣的是,有报道称人类“8”字形孵化囊胚的内细胞团(ICM)分裂导致了MZT。然而,MZT的潜在原因尚不清楚。在本研究中,我们在小鼠模型中研究了体外培养是否会导致ICM分裂及其与孵化类型的关系。在以下情况中观察到囊胚孵化:(i)体内发育的囊胚,以及(ii-iii)体内或体外受精后的体外培养囊胚。我们发现,两组体外培养的囊胚中“8”字形孵化的发生率显著高于体内发育的囊胚组(分别为24.4%和20.4%,而体内发育的囊胚组为0.8%;n = 805,P < 0.01)。此外,进行了Oct4免疫荧光染色以识别孵化和已孵化囊胚中的ICM。在“8”字形孵化囊胚的小透明带开口周围观察到ICM细胞的分散和分裂分布。这种情况在体外培养组中发生率很高。此外,我们发现“8”字形孵化和已孵化囊胚中双OCT4阳性团块比“U”字形孵化和已孵化囊胚更多,提示ICM分裂增加(分别为12.5%和1.9%;n = 838,P < 0.01)。因此,我们的结果表明,延长体外培养可导致“8”字形孵化的高发生率,并且“8”字形孵化可能会干扰ICM疝出,导致小鼠囊胚中ICM分裂风险增加。这些结果可能为体外受精和囊胚移植后人类MZT风险增加提供见解。