Abstract
Many underlying causes of human infertility have been overcome by using in vitro fertilization (IVF) and embryo transfer (ET) techniques. Nevertheless, implantation rates in IVF programs remain low despite the transfer of apparently healthy embryos. This suggests that there are problems with the differentiation of the uterus to the receptive state in response to the ovarian hormones estrogen and progesterone. The molecular basis of this receptive state when the uterine environment is conducive to blastocyst acceptance and implantation remains poorly understood. Normally, the "window" of uterine receptivity lasts for a limited time. Using ETs and the progesterone-treated delayed-implantation model in mice, we demonstrate here that levels of estrogen within a very narrow range determine the duration of the window of uterine receptivity. Although estrogen at different physiological concentrations can initiate implantation, we find that the window of uterine receptivity remains open for an extended period at lower estrogen levels but rapidly closes at higher levels. The uterine refractoriness that follows the receptive state at high estrogen levels is accompanied by aberrant uterine expression of implantation-related genes. These results suggest that careful regulation of estrogen levels is one of the important factors for improvement of female fertility in IVFET programs.
MeSH Terms
Animals
Blastocyst/drug effects,physiology
Embryo Implantation
Embryo Transfer
Estradiol/pharmacology
Estrogens/physiology
Female
Gene Expression Regulation
In Situ Hybridization
Male
Mice
Mice, Inbred Strains
Pregnancy
RNA, Complementary/metabolism
Time Factors
Uterus/metabolism
Chemicals
Estrogens
RNA, Complementary
Estradiol
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ma Wen-ge
Division of Reproductive and Developmental Biology and Department of Pediatric, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Song Haengseok
Das Sanjoy K
Paria Bibhash C
Dey Sudhansu K
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