Eight-Shaped Hatching Increases the Risk of Inner Cell Mass Splitting in Extended Mouse Embryo Culture

PLoS One. 2015 Dec 17;10(12):e0145172. doi: 10.1371/journal.pone.0145172. eCollection 2015.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastocyst Inner Cell Mass / cytology
  • Blastocyst Inner Cell Mass / metabolism
  • Blastocyst Inner Cell Mass / physiology*
  • Cell Division
  • Cells, Cultured
  • Embryo Culture Techniques / methods*
  • Mice
  • Octamer Transcription Factor-3 / metabolism

Substances

  • Octamer Transcription Factor-3
  • Pou5f1 protein, mouse

Grants and funding

This research was supported by the Natural Science Foundation of Shanghai, China (15ZR1424900) URL: http://www.stcsm.gov.cn/, role:design the study, decision to publish, and preparation of the manuscript, the National Natural Science Foundation for the Youth of China (81300485) URL: http://www.nsfc.gov.cn/, role:perform the study, decision to publish, and preparation of the manuscript, and the National Natural Science Foundation of China (31071275, 81571486), URL: http://www.nsfc.gov.cn/, role:design the study, data collection and analysis and preparation of the manuscript.