Effect of Estradiol on Mouse Uterine Epithelial Cell Transepithelial Resistance (TER)
Article first published online: 18 OCT 2004
American Journal of Reproductive Immunology
Volume 52, Issue 4, pages 252–262, October 2004
How to Cite
Grant-Tschudy, K. S. and Wira, C. R. (2004), Effect of Estradiol on Mouse Uterine Epithelial Cell Transepithelial Resistance (TER). American Journal of Reproductive Immunology, 52: 252–262. doi: 10.1111/j.1600-0897.2004.00218.x
- Issue published online: 18 OCT 2004
- Article first published online: 18 OCT 2004
- Submitted June 11, 2004; revised July 15, 2004; accepted August 3, 2004.
- Epithelial cells;
- transepithelial resistance;
Problem: The effects of estradiol on epithelial cell function in the uterus may either be direct or indirect through the paracrine effects of underlying stromal cells. The aim of this study was to test whether estradiol-17β (E2) acts directly to regulate uterine epithelial cell monolayer integrity.
Methods of Study: Mouse uterine epithelial cells were isolated and grown on cell culture inserts to form confluent, polarized monolayers, as indicated by the development of high transepithelial resistance (TER).
Results: When polarized epithelial cells were treated with E2, TER was significantly decreased within 24 hr of exposure. Epithelial cells remained hormonally responsive in culture for at least 10 days. In contrast to estradiol, incubation with progesterone, cortisol, aldosterone, and DHT had no effect on uterine epithelial cell TER. The ability of E2 to decrease TER was inhibited following co-incubation with ICI 182,780, a pure estrogen receptor antagonist. To further investigate the mechanism involved in estradiol-induced decreases in TER, we tested the effect of TAPI-0, an inhibitor of matrix metalloproteinases. Our findings indicate that TAPI-0 reversed the inhibitory effect of E2 on TER.
Conclusions: These studies demonstrate that epithelial monolayer integrity is directly influenced by E2 and ER mediated. Further, it suggests that the mechanism through which estradiol decreases TER is mediated by matrix metalloproteinases.