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Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development
Background: Intercellular communication between epithelial and mesenchymal cells is central to mammalian craniofacial development. β-catenin is the gateway of canonical Wnt signaling, one of the major evolutionarily conserved cell–cell communication pathways in metazoa. In this study, we report an u...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley-Liss, Inc.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308359/ https://www.ncbi.nlm.nih.gov/pubmed/22354888 http://dx.doi.org/10.1002/dvdy.23755 |
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author | Sun, Ye Teng, Ian Huo, Randi Rosenfeld, Michael G Olson, Lorin E Li, Xiaokun Li, Xue |
author_facet | Sun, Ye Teng, Ian Huo, Randi Rosenfeld, Michael G Olson, Lorin E Li, Xiaokun Li, Xue |
author_sort | Sun, Ye |
collection | PubMed |
description | Background: Intercellular communication between epithelial and mesenchymal cells is central to mammalian craniofacial development. β-catenin is the gateway of canonical Wnt signaling, one of the major evolutionarily conserved cell–cell communication pathways in metazoa. In this study, we report an unexpected stage- and tissue-specific function of β-catenin during mammalian jaw development. Results: Using a unique mouse genetic tool, we have discovered that epithelial β-catenin is essential for lower jaw formation, while attenuation of β-catenin is required for proper upper jaw development. Changes in β-catenin in vivo alter major epithelial Fgf8, Bmp4, Shh, and Edn1 signals, resulting in partial transcriptional reprogramming of the neural crest-derived mesenchyme, the primary source of jawbones. Conclusions: The Wnt/β-catenin signal coordinates expression of multiple epithelial signals and has stage-specific asymmetric functions during mammalian upper and lower jaw development. In addition, these findings suggest that evolutionary changes of the canonical Wnt/β-catenin signaling pathway may lead to innovation of jaws. Developmental Dynamics 241:663–674, 2012. © 2012 Wiley Periodicals, Inc. KEY FINDINGS: Mammalian epithelial Wnt/β-catenin signaling has asymetric functions in the upper and lower jaw development. The canonical Wnt/β-catenin pathway coordinates expression of multiple epithelial signals including Fgf8, Bmp4, Shh, and Edn1. Activation of epithelial Wnt/β-catenin signaling induces molecular transformation of the upper jaw to the lower jaw mesenchymal phenotype. Evolutionary changes of the canonical Wnt/β-catenin signaling pathway may lead to innovation of jaws. |
format | Online Article Text |
id | pubmed-3308359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Wiley-Liss, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-33083592013-02-08 Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development Sun, Ye Teng, Ian Huo, Randi Rosenfeld, Michael G Olson, Lorin E Li, Xiaokun Li, Xue Dev Dyn Research Articles Background: Intercellular communication between epithelial and mesenchymal cells is central to mammalian craniofacial development. β-catenin is the gateway of canonical Wnt signaling, one of the major evolutionarily conserved cell–cell communication pathways in metazoa. In this study, we report an unexpected stage- and tissue-specific function of β-catenin during mammalian jaw development. Results: Using a unique mouse genetic tool, we have discovered that epithelial β-catenin is essential for lower jaw formation, while attenuation of β-catenin is required for proper upper jaw development. Changes in β-catenin in vivo alter major epithelial Fgf8, Bmp4, Shh, and Edn1 signals, resulting in partial transcriptional reprogramming of the neural crest-derived mesenchyme, the primary source of jawbones. Conclusions: The Wnt/β-catenin signal coordinates expression of multiple epithelial signals and has stage-specific asymmetric functions during mammalian upper and lower jaw development. In addition, these findings suggest that evolutionary changes of the canonical Wnt/β-catenin signaling pathway may lead to innovation of jaws. Developmental Dynamics 241:663–674, 2012. © 2012 Wiley Periodicals, Inc. KEY FINDINGS: Mammalian epithelial Wnt/β-catenin signaling has asymetric functions in the upper and lower jaw development. The canonical Wnt/β-catenin pathway coordinates expression of multiple epithelial signals including Fgf8, Bmp4, Shh, and Edn1. Activation of epithelial Wnt/β-catenin signaling induces molecular transformation of the upper jaw to the lower jaw mesenchymal phenotype. Evolutionary changes of the canonical Wnt/β-catenin signaling pathway may lead to innovation of jaws. Wiley-Liss, Inc. 2012-04 2012-02-21 /pmc/articles/PMC3308359/ /pubmed/22354888 http://dx.doi.org/10.1002/dvdy.23755 Text en Copyright © 2012 Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Research Articles Sun, Ye Teng, Ian Huo, Randi Rosenfeld, Michael G Olson, Lorin E Li, Xiaokun Li, Xue Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development |
title | Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development |
title_full | Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development |
title_fullStr | Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development |
title_full_unstemmed | Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development |
title_short | Asymmetric Requirement of Surface Epithelial β-Catenin During the Upper and Lower Jaw Development |
title_sort | asymmetric requirement of surface epithelial β-catenin during the upper and lower jaw development |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308359/ https://www.ncbi.nlm.nih.gov/pubmed/22354888 http://dx.doi.org/10.1002/dvdy.23755 |
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