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Abstract
Beta-cateninthe mammalian homolog of
Drosophila armadillo protein, was first identified
as a cadherin-associated protein at cell-cell junctions.
Another function of beta-catenin is the transduction of
cytosolic signals to the nucleus in a variety of cellular
contexts, which are usually elicited by the active form of
beta-catenin. The aim of this study was to examine the
potential role of active beta-catenin in the mouse embryo
and uterus during embryo implantation. As shown by these
results, active beta-catenin was detected differentially
in mouse embryos and uteri during the periimplantation
period. Aberrant activation of beta-catenin by LiCl, a
well-known GSK3 (glycogen synthase kinase3) inhibitor,
significantly inhibited blastocyst hatching and subsequent
adhesion and outgrowth on FN (fibronectin). Results
obtained from pseudopregnant and implantation-delayed mice
imply an important role for implanting blastocysts on the
temporal and spatial changes of active beta-catenin in the
uterus during the window of implantation. Collectively,
these results suggest that the beta-catenin signaling
pathway is inhibited in both blastocyst and uterus during
the window of implantation, which may represent a new
mechanism to synchronize the development of
preimplantation embryos and differentiation of the uterus
during this process.
Key words:
Embryo
Pregnancy
Implantation
Signal transduction
Steroid hormones
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