Knockdown of the tetraspan protein epithelial membrane protein-2 inhibits implantation in the mouse

被引:38
|
作者
Wadehra, M
Dayal, M
Mainigi, M
Ord, T
Iyer, R
Braun, J
Williams, CJ
机构
[1] Univ Calif Los Angeles, Geffen Sch Med, Dept Pathol & Lab Med, Inst Mol Biol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Johnson Comprehens Canc Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[3] Univ Penn, Ctr Res Reprod & Womens Hlth, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Obstet & Gynecol, Div Reprod Endocrinol & Infertil, Philadelphia, PA 19104 USA
关键词
epithelial membrane protein-2; tetraspan; implantation; endometrum; protein trafficking; GAS3/PMP22;
D O I
10.1016/j.ydbio.2006.01.015
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The establishment of pregnancy requires a successful molecular interaction between the trophectoderm cells of the blastocyst stage embryo and the endometrial cells of the uterus. These interactions are complex and require synchronous development and coordinated endocrine, paracrine, and autocrine communication. In this study, we demonstrate that the tetraspan protein epithelial membrane protein-2 (EMP2) is involved in these molecular interactions during implantation. EMP2, which is highly expressed in the uterus, translocates from an intracellular location to the apical surface of the endometrial epithelium during the window of implantation and is expressed in decidualized stromal cells. We developed plasmid constructs that utilized either ribozyme-mediated or short hairpin RNA-mediated mechanisms to target endometrial EMP2 mRNA for destruction. These constructs were transfected into the mouse uterus on day I of pregnancy using the technique of in vivo reproductive tract gene transfer. Reduction in EMP2 expression by either method resulted in a significant decrease in the number of implantation sites in the treated uterine horns as compared to control horns. These studies indicate a previously unknown function of tetraspan proteins in implantation and could provide a molecular framework for the development of therapeutic modalities for both contraception and fertility. (c) 2006 Elsevier Inc. All rights reserved.
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页码:430 / 441
页数:12
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