Modeling embryo-endometrial interface recapitulating human embryo implantation

Author:

Shibata Shun12ORCID,Endo Shun13ORCID,Nagai Luis A. E.4ORCID,H. Kobayashi Eri1ORCID,Oike Akira15,Kobayashi Norio16ORCID,Kitamura Akane1,Hori Takeshi7ORCID,Nashimoto Yuji7ORCID,Nakato Ryuichiro4ORCID,Hamada Hirotaka3ORCID,Kaji Hirokazu7ORCID,Kikutake Chie8ORCID,Suyama Mikita8ORCID,Saito Masatoshi3,Yaegashi Nobuo3ORCID,Okae Hiroaki15ORCID,Arima Takahiro1ORCID

Affiliation:

1. Department of Informative Genetics, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

2. Research and Development Division, Rohto Pharmaceutical Co. Ltd., Osaka 544-8666, Japan.

3. Department of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

4. Laboratory of Computational Genomics, Institute for Quantitative Biosciences, The University of Tokyo, Tokyo 113-0032, Japan.

5. Department of Trophoblast Research, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto 862-0973, Japan.

6. Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.

7. Department of Diagnostic and Therapeutic Systems Engineering, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, Tokyo 101-0062, Japan.

8. Division of Bioinformatics, Medical Institute of Bioregulation, Kyushu University, Fukuoka 812-8582, Japan.

Abstract

The initiation of human pregnancy is marked by the implantation of an embryo into the uterine environment; however, the underlying mechanisms remain largely elusive. To address this knowledge gap, we developed hormone-responsive endometrial organoids (EMO), termed apical-out (AO)–EMO, which emulate the in vivo architecture of endometrial tissue. The AO-EMO comprise an exposed apical epithelium surface, dense stromal cells, and a self-formed endothelial network. When cocultured with human embryonic stem cell–derived blastoids, the three-dimensional feto-maternal assembloid system recapitulates critical implantation stages, including apposition, adhesion, and invasion. Endometrial epithelial cells were subsequently disrupted by syncytial cells, which invade and fuse with endometrial stromal cells. We validated this fusion of syncytiotrophoblasts and stromal cells using human blastocysts. Our model provides a foundation for investigating embryo implantation and feto-maternal interactions, offering valuable insights for advancing reproductive medicine.

Publisher

American Association for the Advancement of Science (AAAS)

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