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Mechanics of mouse blastocyst hatching revealed by a hydrogel-based microdeformation assay

Abstract:
Mammalian embryos are surrounded by an acellular shell, the zona pellucida. Hatching out of the zona is crucial for implantation and continued development of the embryo. Clinically, problems in hatching can contribute to failure in assisted reproductive intervention. Although hatching is fundamentally a mechanical process, due to limitations in methodology most studies focus on its biochemical properties. To understand the role of mechanical forces in hatching, we developed a hydrogel deformation-based method and analytical approach for measuring pressure in cyst-like tissues. Using this approach, we found that, in cultured blastocysts, pressure increased linearly, with intermittent falls. Inhibition of Na/K-ATPase led to a dosage-dependent reduction in blastocyst cavity pressure, consistent with its requirement for cavity formation. Reducing blastocyst pressure reduced the probability of hatching, highlighting the importance of mechanical forces in hatching. These measurements allowed us to infer details of microphysiology such as osmolarity, ion and water transport kinetics across the trophectoderm, and zona stiffness, allowing us to model the embryo as a thin-shell pressure vessel. We applied this technique to test whether cryopreservation, a process commonly used in assisted reproductive technology (ART), leads to alteration of the embryo and found that thawed embryos generated significantly lower pressure than fresh embryos, a previously unknown effect of cryopreservation. We show that reduced pressure is linked to delayed hatching. Our approach can be used to optimize in vitro fertilization (IVF) using precise measurement of embryo microphysiology. It is also applicable to other biological systems involving cavity formation, providing an approach for measuring forces in diverse contexts.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1073/pnas.1719930115

Authors

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Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Physiology Anatomy and Genetics
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Role:
Author
More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author
More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author
ORCID:
0000-0003-3623-600X


More from this funder
Funding agency for:
Leonavicius, K
Srinivas, S
Grant:
203141/Z/16/Z
Senior Investigator Award (103788/Z/14/Z
More from this funder
Funding agency for:
Leonavicius, K
Grant:
203141/Z/16/Z
More from this funder
Funding agency for:
Leonavicius, K
Grant:
203141/Z/16/Z


Publisher:
National Academy of Sciences
Journal:
Proceedings of the National Academy of Sciences More from this journal
Volume:
115
Issue:
41
Pages:
10375-10380
Publication date:
2018-09-19
Acceptance date:
2018-08-15
DOI:
EISSN:
1091-6490
ISSN:
0027-8424
Pmid:
30232257


Language:
English
Keywords:
Pubs id:
pubs:920894
UUID:
uuid:1c1f844a-09ce-49b0-be61-0838b3ff03ce
Local pid:
pubs:920894
Source identifiers:
920894
Deposit date:
2018-10-25
ARK identifier:

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