Dissecting the impact of endometriosis on decidualization and trophoblast-endometrial interactions. - implantation is a critical process in human development, initiated when the blastocyst-stage…
Active Project Grant Awarded Last action
- Award ID
- F31HD121162
- Recipient
-
Yale Univ UEI FL6GV84CKN57
- Awarding agency
-
National Institute of Child Health and Human Development
National Institutes of Health, Department of Health and Human Services
- Obligated
- $158,766
Award facts
- Assistance listing
- 93.865 Child Health and Human Development Extramural Research
- Completion date 34% complete
- Originally
- Place of performance
- New Haven, CT 06510, USA
Award details come from USAspending.gov.
Description
Dissecting the impact of endometriosis on decidualization and trophoblast-endometrial interactions. - implantation is a critical process in human development, initiated when the blastocyst-stage embryo establishes contact with the maternal endometrium. This interaction is mediated by trophoblast cells from the trophectoderm, which regulate early invasion and maternal-fetal crosstalk. Disruptions in trophoblast- endometrium interactions can lead to implantation failure, pregnancy loss, and complications such as preeclampsia. Women with endometriosis, a systemic condition affecting millions in the U.S., face an increased risk of infertility and pregnancy complications. However, the molecular mechanisms underlying these issues remain poorly understood, highlighting the need for models that accurately replicate trophoblast-endometrium dynamics in both healthy and diseased states. Existing in vitro models lack critical architectural and functional features, limiting their translational relevance. To address this GAP, I developed a novel patient-derived 3D endometrial assembloid (EMA) that mimics key aspects of endometrial architecture, including epithelial, stromal, and uterine endothelial cells; hormone responsiveness; basement membrane secretion; and apical-out polarity. This platform enables physiologically relevant studies of trophoblast-endometrium interactions. This proposal will investigate the role of mirnas in decidualization within the context of endometriosis, and how the disease affects trophoblast development and invasion. I propose to integrate advanced 3D tissue engineering, high-resolution imaging, extracellular vesicle analysis, and transcriptomic/functional assays to explore how endometriosis-associated decidualization defects influence trophoblast behavior. This study will provide insights into the mechanisms driving implantation defects and pregnancy complications by addressing fundamental questions about trophoblast-endometrium interactions in the context of endometriosis. Ultimately, these findings will be critical for the possible prevention of adverse pregnancy outcomes, offering a unique opportunity to inform future diagnostic and therapeutic strategies for improving reproductive outcomes in endometriosis patients.
Transactions
| Action | Obligated | Date |
|---|---|---|
| Amendment | $576 | |
| Amendment | $576 | |
| Amendment | $0 | |
| Amendment | $52,538 | |
| Amendment | $52,538 | |
| Original award | $52,538 |
Quick answers
Who received award F31HD121162?
F31HD121162 was awarded to Yale Univ by National Institute of Child Health and Human Development (National Institutes of Health) on August 1, 2025.
How much is award F31HD121162 worth?
$158,766 has been obligated on F31HD121162.
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