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Uterine Gα q/11 signaling, in a progesterone‐dependent manner, critically regulates the acquisition of uterine receptivity in the female mouse
Author(s) -
Oliveira Vanessa,
Schaefer Jennifer,
Calder Michele,
Lydon John P.,
Demayo Francesco J.,
Bhattacharya Moshmi,
Radovick Sally,
Babwah Andy V.
Publication year - 2019
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.201900026r
Subject(s) - endocrinology , biology , medicine , signal transduction , uterus , receptor , knockout mouse , progesterone receptor , receptivity , microbiology and biotechnology , myometrium , cancer , estrogen receptor , breast cancer
A nonreceptive uterus is a major cause of embryo implantation failure. This study examined the importance of the Gα q/11 ‐coupled class of GPCRs as regulators of uterine receptivity. Mice were created lacking uterine Gα q and Gα 11 ; as a result, signaling by all uterine Gα q/11 ‐coupled receptors was disrupted. Reproductive profiling of the knockout females revealed that on d 4 of pregnancy, despite adequate serum progesterone (P4) levels and normal P4 receptor (PR) expression, there was no evidence of PR signaling. This resulted in the down‐regulation of heart and neural crest derivatives expressed 2, Kruppel‐like factor 15, and cyclin G1 and the subsequent persistent proliferation of the luminal epithelium. Aquaporin (Aqp) 11 was also potently down‐regulated, whereas Aηp5 /AQP5 expression persisted, resulting in the inhibition of luminal closure. Hypertrophy of the myometrial longitudinal muscle was also dramatically diminished, likely contributing to the observed implantation failure. Further analyses revealed that a major mechanism via which uterine Gα q/11 signaling induces PR signaling is through the transcriptional up‐regulation of leucine‐rich repeat‐containing GPCR 4 ( Lgr4 ). LGR4 was previously identified as a trigger of PR activation and signaling. Overall, this study establishes that Gα q/11 signaling, in a P4‐dependent manner, critically regulates the acquisition of uterine receptivity in the female mouse, and disruption of such signaling results in P4 resistance.—de Oliveira, V., Schaefer, J., Calder, M., Lydon, J. P., DeMayo, F. J., Bhattacharya, M., Radovick, S., Babwah, A. V. Uterine Gα q/11 signaling, in a progesterone‐dependent manner, critically regulates the acquisition of uterine receptivity in the female mouse. FASEB J. 33, 9374–9387 (2019). www.fasebj.org