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Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease
The establishment of polarity within tissues and dynamic cellular morphogenetic events are features common to both developing and adult tissues, and breakdown of these programs is associated with diverse human diseases. Wnt/Planar cell polarity (Wnt/PCP) signaling, a branch of non-canonical Wnt sign...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130715/ https://www.ncbi.nlm.nih.gov/pubmed/35646914 http://dx.doi.org/10.3389/fcell.2022.887100 |
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author | Dreyer, Courtney A. VanderVorst, Kacey Carraway, Kermit L. |
author_facet | Dreyer, Courtney A. VanderVorst, Kacey Carraway, Kermit L. |
author_sort | Dreyer, Courtney A. |
collection | PubMed |
description | The establishment of polarity within tissues and dynamic cellular morphogenetic events are features common to both developing and adult tissues, and breakdown of these programs is associated with diverse human diseases. Wnt/Planar cell polarity (Wnt/PCP) signaling, a branch of non-canonical Wnt signaling, is critical to the establishment and maintenance of polarity in epithelial tissues as well as cell motility events critical to proper embryonic development. In epithelial tissues, Wnt/PCP-mediated planar polarity relies upon the asymmetric distribution of core proteins to establish polarity, but the requirement for this distribution in Wnt/PCP-mediated cell motility remains unclear. However, in both polarized tissues and migratory cells, the Wnt/PCP-specific transmembrane protein Vangl is required and appears to serve as a scaffold upon which the core pathway components as well as positive and negative regulators of Wnt/PCP signaling assemble. The current literature suggests that the multiple interaction domains of Vangl allow for the binding of diverse signaling partners for the establishment of context- and tissue-specific complexes. In this review we discuss the role of Vangl as a master scaffold for Wnt/PCP signaling in epithelial tissue polarity and cellular motility events in developing and adult tissues, and address how these programs are dysregulated in human disease. |
format | Online Article Text |
id | pubmed-9130715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91307152022-05-26 Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease Dreyer, Courtney A. VanderVorst, Kacey Carraway, Kermit L. Front Cell Dev Biol Cell and Developmental Biology The establishment of polarity within tissues and dynamic cellular morphogenetic events are features common to both developing and adult tissues, and breakdown of these programs is associated with diverse human diseases. Wnt/Planar cell polarity (Wnt/PCP) signaling, a branch of non-canonical Wnt signaling, is critical to the establishment and maintenance of polarity in epithelial tissues as well as cell motility events critical to proper embryonic development. In epithelial tissues, Wnt/PCP-mediated planar polarity relies upon the asymmetric distribution of core proteins to establish polarity, but the requirement for this distribution in Wnt/PCP-mediated cell motility remains unclear. However, in both polarized tissues and migratory cells, the Wnt/PCP-specific transmembrane protein Vangl is required and appears to serve as a scaffold upon which the core pathway components as well as positive and negative regulators of Wnt/PCP signaling assemble. The current literature suggests that the multiple interaction domains of Vangl allow for the binding of diverse signaling partners for the establishment of context- and tissue-specific complexes. In this review we discuss the role of Vangl as a master scaffold for Wnt/PCP signaling in epithelial tissue polarity and cellular motility events in developing and adult tissues, and address how these programs are dysregulated in human disease. Frontiers Media S.A. 2022-05-11 /pmc/articles/PMC9130715/ /pubmed/35646914 http://dx.doi.org/10.3389/fcell.2022.887100 Text en Copyright © 2022 Dreyer, VanderVorst and Carraway. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Dreyer, Courtney A. VanderVorst, Kacey Carraway, Kermit L. Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease |
title | Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease |
title_full | Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease |
title_fullStr | Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease |
title_full_unstemmed | Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease |
title_short | Vangl as a Master Scaffold for Wnt/Planar Cell Polarity Signaling in Development and Disease |
title_sort | vangl as a master scaffold for wnt/planar cell polarity signaling in development and disease |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130715/ https://www.ncbi.nlm.nih.gov/pubmed/35646914 http://dx.doi.org/10.3389/fcell.2022.887100 |
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