Journal
EXPERIMENTAL BIOLOGY AND MEDICINE
Volume 242, Issue 18, Pages 1735-1745Publisher
SAGE PUBLICATIONS LTD
DOI: 10.1177/1535370217732737
Keywords
beta-catenin; Wnt signaling; cardiogenesis; plakoglobin; development; heart
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Funding
- EU FP7 Grant Fishmed GA [316125]
- Polish National Science Center (NCN) OPUS grant [2014/13/B/NZ2/03863]
- EMBO [ASTF 518-2015]
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The main mediator of the canonical Wnt pathway, beta-catenin, is a major effector of embryonic development, postnatal tissue homeostasis, and adult tissue regeneration. The requirement for -beta catenin in cardiogenesis and embryogenesis has been well established. However, many questions regarding the molecular mechanisms by which beta-catenin and canonical Wnt signaling regulate these developmental processes remain unanswered. An interesting question that emerged from our studies concerns how beta-catenin signaling is modulated through interaction with other factors. Recent experimental data implicate new players in canonical Wnt signaling, particularly those which modulate beta-catenin function in many its biological processes, including cardiogenesis. One of the interesting candidates is plakoglobin, a little-studied member of the catenin family which shares several mechanistic and functional features with its close relative, beta-catenin. Here we have focused on the function of beta-catenin in cardiogenesis. We also summarize findings on plakoglobin signaling function and discuss possible interplays between beta-catenin and plakoglobin in the regulation of embryonic heart development.
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