TY - JOUR
T1 - Modeling embryo-endometrial interface recapitulating human embryo implantation
AU - Shibata, Shun
AU - Endo, Shun
AU - Nagai, Luis A.E.
AU - Kobayashi, Eri H.
AU - Oike, Akira
AU - Kobayashi, Norio
AU - Kitamura, Akane
AU - Hori, Takeshi
AU - Nashimoto, Yuji
AU - Nakato, Ryuichiro
AU - Hamada, Hirotaka
AU - Kaji, Hirokazu
AU - Kikutake, Chie
AU - Suyama, Mikita
AU - Saito, Masatoshi
AU - Yaegashi, Nobuo
AU - Okae, Hiroaki
AU - Arima, Takahiro
N1 - Publisher Copyright:
copyright © 2024 the Authors, some rights reserved.
PY - 2024/2
Y1 - 2024/2
N2 - 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.
AB - 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.
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U2 - 10.1126/sciadv.adi4819
DO - 10.1126/sciadv.adi4819
M3 - Article
C2 - 38394208
AN - SCOPUS:85185900302
SN - 2375-2548
VL - 10
JO - Science advances
JF - Science advances
IS - 8
M1 - eadi4819
ER -