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Review

Engineering the Human Endometrial–Embryo Interface: Breakthroughs in 3D Uterine Models

by
Jenna A. Douglas
1,2,†,
Jordan Higgins
3,†,
Dinasha H. Wimalasiri
1,2,
Amy L. Winship
3 and
Harriet C. Fitzgerald
1,2,*
1
Department of Obstetrics and Gynaecology, Monash University, Clayton, VIC 3168, Australia
2
The Ritchie Centre, Hudson Institute of Medical Research, Clayton, VIC 3168, Australia
3
Monash Biomedicine Discovery Institute, Department of Anatomy and Developmental Biology, Development and Stem Cells Program, Monash University, Clayton, VIC 3800, Australia
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Biomolecules 2026, 16(3), 383; https://doi.org/10.3390/biom16030383
Submission received: 16 January 2026 / Revised: 16 February 2026 / Accepted: 24 February 2026 / Published: 3 March 2026

Abstract

Three-dimensional (3D) organoid and co-culture models have emerged as transformative tools for studying human endometrial function, implantation, and placental development, overcoming key limitations of animal and two-dimensional in vitro systems. This review synthesises available information of recent advances in endometrial epithelial organoids (EEOs), trophoblast organoids (TBOs), and increasingly complex co-culture platforms incorporating stromal, vascular, and trophoblast compartments to model epithelial–stromal crosstalk, decidualisation, angiogenesis, and embryo implantation. Emerging developments include assembloid systems, synthetic and semi-synthetic extracellular matrices, and microfluidic organ-on-a-chip technologies that enable long-term culture, hormonal responsiveness, and patient-specific modelling. These approaches have recapitulated key features of the mid-secretory endometrium, placental villous architecture, trophoblast differentiation, and early implantation events while revealing disease-associated dysfunctions in conditions such as endometriosis, adenomyosis, polycystic ovarian syndrome, and endometrial cancer. Despite significant progress, current models remain limited by incomplete cellular diversity, polarity constraints, and challenges in fully modelling immune and vascular interactions. Collectively, emerging 3D organoid and co-culture systems provide physiologically relevant platforms to interrogate human reproductive biology, elucidate mechanisms underlying implantation failure and placental disease, and support the development of personalised therapeutic strategies to improve reproductive outcomes.
Keywords: endometrium; endometrial epithelial organoids; uterus; embryo implantation; placenta; trophoblast organoids endometrium; endometrial epithelial organoids; uterus; embryo implantation; placenta; trophoblast organoids

Share and Cite

MDPI and ACS Style

Douglas, J.A.; Higgins, J.; Wimalasiri, D.H.; Winship, A.L.; Fitzgerald, H.C. Engineering the Human Endometrial–Embryo Interface: Breakthroughs in 3D Uterine Models. Biomolecules 2026, 16, 383. https://doi.org/10.3390/biom16030383

AMA Style

Douglas JA, Higgins J, Wimalasiri DH, Winship AL, Fitzgerald HC. Engineering the Human Endometrial–Embryo Interface: Breakthroughs in 3D Uterine Models. Biomolecules. 2026; 16(3):383. https://doi.org/10.3390/biom16030383

Chicago/Turabian Style

Douglas, Jenna A., Jordan Higgins, Dinasha H. Wimalasiri, Amy L. Winship, and Harriet C. Fitzgerald. 2026. "Engineering the Human Endometrial–Embryo Interface: Breakthroughs in 3D Uterine Models" Biomolecules 16, no. 3: 383. https://doi.org/10.3390/biom16030383

APA Style

Douglas, J. A., Higgins, J., Wimalasiri, D. H., Winship, A. L., & Fitzgerald, H. C. (2026). Engineering the Human Endometrial–Embryo Interface: Breakthroughs in 3D Uterine Models. Biomolecules, 16(3), 383. https://doi.org/10.3390/biom16030383

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