Embryo‐uterine interaction coordinates mouse embryogenesis during implantation

Author:

Bondarenko Vladyslav12ORCID,Nikolaev Mikhail3,Kromm Dimitri4ORCID,Belousov Roman4ORCID,Wolny Adrian4ORCID,Blotenburg Marloes5,Zeller Peter5,Rezakhani Saba3,Hugger Johannes46ORCID,Uhlmann Virginie6,Hufnagel Lars4,Kreshuk Anna4,Ellenberg Jan4,van Oudenaarden Alexander5,Erzberger Anna47ORCID,Lutolf Matthias P3ORCID,Hiiragi Takashi1589ORCID

Affiliation:

1. European Molecular Biology Laboratory Developmental Biology Unit Heidelberg Germany

2. Faculty of Biosciences University of Heidelberg Heidelberg Germany

3. Institute of Bioengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL) Lausanne Switzerland

4. European Molecular Biology Laboratory, Cell Biology and Biophysics Unit Heidelberg Germany

5. Hubrecht Institute Utrecht The Netherlands

6. EMBL‐EBI, Wellcome Genome Campus Hinxton UK

7. Department of Physics and Astronomy Heidelberg University Heidelberg Germany

8. Institute for the Advanced Study of Human Biology (WPI‐ASHBi) Kyoto University Kyoto Japan

9. Department of Developmental Biology Graduate School of Medicine, Kyoto University Kyoto Japan

Abstract

AbstractEmbryo implantation into the uterus marks a key transition in mammalian development. In mice, implantation is mediated by the trophoblast and is accompanied by a morphological transition from the blastocyst to the egg cylinder. However, the roles of trophoblast‐uterine interactions in embryo morphogenesis during implantation are poorly understood due to inaccessibility in utero and the remaining challenges to recapitulate it ex vivo from the blastocyst. Here, we engineer a uterus‐like microenvironment to recapitulate peri‐implantation development of the whole mouse embryo ex vivo and reveal essential roles of the physical embryo‐uterine interaction. We demonstrate that adhesion between the trophoblast and the uterine matrix is required for in utero‐like transition of the blastocyst to the egg cylinder. Modeling the implanting embryo as a wetting droplet links embryo shape dynamics to the underlying changes in trophoblast adhesion and suggests that the adhesion‐mediated tension release facilitates egg cylinder formation. Light‐sheet live imaging and the experimental control of the engineered uterine geometry and trophoblast velocity uncovers the coordination between trophoblast motility and embryo growth, where the trophoblast delineates space for embryo morphogenesis.

Funder

European Molecular Biology Laboratory

Joachim Herz Stiftung

Publisher

Springer Science and Business Media LLC

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3