An In Vitro Model for the Study of Human Implantation

被引:36
|
作者
Holmberg, Jennie C.
Haddad, Severina
Wuensche, Vera
Yang, Yang
Aldo, Paulomi B.
Gnainsky, Yulia [2 ]
Granot, Irit [3 ]
Dekel, Nava [2 ]
Mor, Gil [1 ]
机构
[1] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, Reprod Immunol Unit, New Haven, CT 06520 USA
[2] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
[3] Kaplan Med Ctr, IVF Unit, Dept Obstet & Gynecol, Rehovot, Israel
基金
美国国家科学基金会;
关键词
Epithelium; inflammation; implantation; stroma; trophoblast; EMBRYO IMPLANTATION; BLASTOCYST IMPLANTATION; ENDOMETRIAL RECEPTIVITY; BREAST-CANCER; STEM-CELLS; UTERINE; TROPHOBLAST; EXPRESSION; MOLECULES; FERTILIZATION;
D O I
10.1111/j.1600-0897.2011.01095.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Problem Implantation remains the rate-limiting step for the success of in vitro fertilization. Appropriate models to study the molecular aspects of human implantation are necessary in order to improve fertility. Methods First trimester trophoblast cells are differentiated into blastocyst-like spheroids (BLS) by culturing them in low attachment plates. Immortalized human endometrial stromal cells and epithelial cells (ECC-1) were stably transfected with GFP or tdTomato. Co-culture experiments were monitored using Volocity imaging analysis system. Results This method demonstrates attachment and invasion of BLS, formed by trophoblast cells, into stromal cells, but not to uterine epithelial cells. Conclusion We have developed an in vitro model of uterine implantation. The manipulation of this system allows for dual color monitoring of the cells over time. Additionally, specific compounds can be added to the culture media to test how this may affect implantation and invasion. This model is a helpful tool in understanding the complexity of human implantation.
引用
收藏
页码:169 / 178
页数:10
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