Mifepristone, but not levonorgestrel, inhibits human blastocyst attachment to an in vitro endometrial three-dimensional cell culture model

被引:123
|
作者
Lalitkumar, P. G. L.
Lalitkumar, S.
Meng, C. X.
Stavreus-Evers, A.
Hambiliki, F.
Bentin-Ley, U.
Gemzell-Danielsson, Kristina [1 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp, Dept Woman & Child Hlth, Div Obstet & Gynecol, S-17176 Stockholm, Sweden
[2] Uppsala Univ, Dept Womens & Childrens Hlth, Uppsala, Sweden
[3] Karolinska Inst, Dept Clin Sci, Div Obstet & Gynecol, Stockholm, Sweden
[4] Danish Fertil Clin, Copenhagen, Denmark
关键词
3D-endometrial cell construct; receptivity markers; mifepristone; levonorgestrel; human blastocyst;
D O I
10.1093/humrep/dem297
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: The use of fertility regulating drugs is limited among various socio-ethnic groups due to limited knowledge about their mechanism of action. This study investigates the effect of levonorgestrel and mifepristone on attachment of human embryos to an in vitro endometrial construct. METHOD: Three-dimensional endometrial constructs were established by co-culturing early luteal phase human endometrial stromal and epithelial cells. Expression of endometrial receptivity markers in this construct were examined by immunohistochemistry. Effects of mifepristone and levonorgestrel on viability and attachment of human blastocysts were investigated. RESULTS: Endometrial constructs expressed the factors involved in endometrial receptivity: estrogen receptor, progesterone receptor, vascular endothelial growth factor, leukemia inhibitory factor, interleukin-1, COX-2, MUC-1 and integrin-alpha(V)beta(3). None of the 15 embryos cultured with mifepristone attached to the endometrial construct (P < 0.01), whereas 10/17 in control, and 6/14 in levonorgestrel, groups attached. The attachment was confirmed by the positive expression of cytokeratin 7 at the attachment site. CONCLUSION: Mifepristone inhibits blastocyst attachment. Levonorgestrel did not impair the attachment of human embryos to the in vitro endometrial construct. This model could be used to understand endometrial receptivity and embryo-endometrial dialog and to develop new fertility regulating substances.
引用
收藏
页码:3031 / 3037
页数:7
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