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Publication : HIF2α in the uterine stroma permits embryo invasion and luminal epithelium detachment.

First Author  Matsumoto L Year  2018
Journal  J Clin Invest Volume  128
Issue  7 Pages  3186-3197
PubMed ID  29911998 Mgi Jnum  J:265444
Mgi Id  MGI:6197599 Doi  10.1172/JCI98931
Citation  Matsumoto L, et al. (2018) HIF2alpha in the uterine stroma permits embryo invasion and luminal epithelium detachment. J Clin Invest 128(7):3186-3197
abstractText  Although it has been reported that hypoxia inducible factor 2 alpha (Hif2a), a major transcriptional factor inducible by low oxygen tension, is expressed in the mouse uterus during embryo implantation, its role in pregnancy outcomes remains unclear. This study aimed to clarify functions of uterine HIF using transgenic mouse models. Mice with deletion of Hif2a in the whole uterus (Hif2a-uKO mice) showed infertility due to implantation failure. Supplementation with progesterone (P4) and leukemia inhibitory factor (LIF) restored decidual growth arrest and aberrant position of implantation sites in Hif2a-uKO mice, respectively, but did not rescue pregnancy failure. Histological analyses in Hif2a-uKO mice revealed persistence of the intact luminal epithelium, which blocked direct contact between stroma and embryo, inactivation of PI3K-AKT pathway (embryonic survival signal), and failed embryo invasion. Mice with stromal deletion of Hif2a (Hif2a-sKO mice) showed infertility with impaired embryo invasion and those with epithelial deletion of Hif2a (Hif2a-eKO mice) showed normal fertility, suggesting the importance of stromal HIF2alpha in embryo invasion. This was reflected in reduced expression of membrane type 2 metalloproteinase (MT2-MMP), lysyl oxidase (LOX), VEGF, and adrenomedullin (ADM) in Hif2a-uKO stroma at the attachment site, suggesting that stromal HIF2alpha regulates these mediators to support blastocyst invasion. These findings provide new insight that stromal HIF2alpha allows trophoblast invasion through detachment of the luminal epithelium and activation of an embryonic survival signal.
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