Abstract
Statement of Purpose: The endometrium, the site of embryo implantation, is a unique, dynamic tissue that undergoes rapid vascular remodeling over the course of the menstrual cycle and pregnancy. Endometrial models are crucial for understanding reproductive disorders, including preeclampsia and endometriosis. They also provide a platform to examine mechanisms underlying vascular remodeling that takes place within the endometrium. While animal models can be used to study dynamic endometrial processes, physiological differences in placentation between animals and humans call into question the relevance of such models. Traditional 2D in vitro models allow researchers to study the endometrium using human cells; however, they do not capture cellular crosstalk in complex microenvironments. Tissue engineered 3D endometrial models would provide new avenues to recapitulate aspects of the in vivo environment while retaining the capability to study cell-cell and cell-matrix interactions in a highly tunable manner. Herein, we describe an adaptable 3D hydrogel model of the endometrium consisting of a coculture of human endometrial stromal cells (HESCs) and human umbilical vein endothelial cells (HUVECs) within a methacrylamide-functionalized gelatin (GelMA) hydrogel. We demonstrate the ability to form vessel structures within this model as well as study the kinetics of trophoblast invasion in 3D. The GelMA hydrogel provides a platform to integrate additional signals from the native tissue microenvironment of the endometrium, namely sex steroid hormones, to examine how the role played by endometrial stromal cell decidualization status (specialized decidual endometrial stromal cells play a critical role in embryo implantation and placentation) affects endothelial cell network formation.
| Original language | English (US) |
|---|---|
| Title of host publication | Society for Biomaterials Annual Meeting and Exposition 2019 |
| Subtitle of host publication | The Pinnacle of Biomaterials Innovation and Excellence - Transactions of the 42nd Annual Meeting |
| Publisher | Society for Biomaterials |
| Number of pages | 1 |
| ISBN (Electronic) | 9781510883901 |
| State | Published - Jan 1 2019 |
| Event | 42nd Society for Biomaterials Annual Meeting and Exposition 2019: The Pinnacle of Biomaterials Innovation and Excellence - Seattle, United States Duration: Apr 3 2019 → Apr 6 2019 |
Publication series
| Name | Transactions of the Annual Meeting of the Society for Biomaterials and the Annual International Biomaterials Symposium |
|---|---|
| Volume | 40 |
| ISSN (Print) | 1526-7547 |
Conference
| Conference | 42nd Society for Biomaterials Annual Meeting and Exposition 2019: The Pinnacle of Biomaterials Innovation and Excellence |
|---|---|
| Country | United States |
| City | Seattle |
| Period | 4/3/19 → 4/6/19 |
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ASJC Scopus subject areas
- Biochemistry
- Biophysics
- Biotechnology
- Biomaterials
- Materials Chemistry
Cite this
Development of a biomaterial model of the decidualized endometrium. / Zambuto, Samantha G.; Harley, Brendan A.
Society for Biomaterials Annual Meeting and Exposition 2019: The Pinnacle of Biomaterials Innovation and Excellence - Transactions of the 42nd Annual Meeting. Society for Biomaterials, 2019. (Transactions of the Annual Meeting of the Society for Biomaterials and the Annual International Biomaterials Symposium; Vol. 40).Research output: Chapter in Book/Report/Conference proceeding › Conference contribution
}
TY - GEN
T1 - Development of a biomaterial model of the decidualized endometrium
AU - Zambuto, Samantha G.
AU - Harley, Brendan A
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Statement of Purpose: The endometrium, the site of embryo implantation, is a unique, dynamic tissue that undergoes rapid vascular remodeling over the course of the menstrual cycle and pregnancy. Endometrial models are crucial for understanding reproductive disorders, including preeclampsia and endometriosis. They also provide a platform to examine mechanisms underlying vascular remodeling that takes place within the endometrium. While animal models can be used to study dynamic endometrial processes, physiological differences in placentation between animals and humans call into question the relevance of such models. Traditional 2D in vitro models allow researchers to study the endometrium using human cells; however, they do not capture cellular crosstalk in complex microenvironments. Tissue engineered 3D endometrial models would provide new avenues to recapitulate aspects of the in vivo environment while retaining the capability to study cell-cell and cell-matrix interactions in a highly tunable manner. Herein, we describe an adaptable 3D hydrogel model of the endometrium consisting of a coculture of human endometrial stromal cells (HESCs) and human umbilical vein endothelial cells (HUVECs) within a methacrylamide-functionalized gelatin (GelMA) hydrogel. We demonstrate the ability to form vessel structures within this model as well as study the kinetics of trophoblast invasion in 3D. The GelMA hydrogel provides a platform to integrate additional signals from the native tissue microenvironment of the endometrium, namely sex steroid hormones, to examine how the role played by endometrial stromal cell decidualization status (specialized decidual endometrial stromal cells play a critical role in embryo implantation and placentation) affects endothelial cell network formation.
AB - Statement of Purpose: The endometrium, the site of embryo implantation, is a unique, dynamic tissue that undergoes rapid vascular remodeling over the course of the menstrual cycle and pregnancy. Endometrial models are crucial for understanding reproductive disorders, including preeclampsia and endometriosis. They also provide a platform to examine mechanisms underlying vascular remodeling that takes place within the endometrium. While animal models can be used to study dynamic endometrial processes, physiological differences in placentation between animals and humans call into question the relevance of such models. Traditional 2D in vitro models allow researchers to study the endometrium using human cells; however, they do not capture cellular crosstalk in complex microenvironments. Tissue engineered 3D endometrial models would provide new avenues to recapitulate aspects of the in vivo environment while retaining the capability to study cell-cell and cell-matrix interactions in a highly tunable manner. Herein, we describe an adaptable 3D hydrogel model of the endometrium consisting of a coculture of human endometrial stromal cells (HESCs) and human umbilical vein endothelial cells (HUVECs) within a methacrylamide-functionalized gelatin (GelMA) hydrogel. We demonstrate the ability to form vessel structures within this model as well as study the kinetics of trophoblast invasion in 3D. The GelMA hydrogel provides a platform to integrate additional signals from the native tissue microenvironment of the endometrium, namely sex steroid hormones, to examine how the role played by endometrial stromal cell decidualization status (specialized decidual endometrial stromal cells play a critical role in embryo implantation and placentation) affects endothelial cell network formation.
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UR - http://www.scopus.com/inward/citedby.url?scp=85065393181&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:85065393181
T3 - Transactions of the Annual Meeting of the Society for Biomaterials and the Annual International Biomaterials Symposium
BT - Society for Biomaterials Annual Meeting and Exposition 2019
PB - Society for Biomaterials
ER -