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Frontal Bone Insufficiency in Gsk3β Mutant Mice

The development of the mammalian skull is a complex process that requires multiple tissue interactions and a balance of growth and differentiation. Disrupting this balance can lead to changes in the shape and size of skull bones, which can have serious clinical implications. For example, insufficien...

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Detalles Bibliográficos
Autores principales: Szabo-Rogers, Heather, Yakob, Wardati, Liu, Karen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757545/
https://www.ncbi.nlm.nih.gov/pubmed/26886780
http://dx.doi.org/10.1371/journal.pone.0149604
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author Szabo-Rogers, Heather
Yakob, Wardati
Liu, Karen J.
author_facet Szabo-Rogers, Heather
Yakob, Wardati
Liu, Karen J.
author_sort Szabo-Rogers, Heather
collection PubMed
description The development of the mammalian skull is a complex process that requires multiple tissue interactions and a balance of growth and differentiation. Disrupting this balance can lead to changes in the shape and size of skull bones, which can have serious clinical implications. For example, insufficient ossification of the bony elements leads to enlarged anterior fontanelles and reduced mechanical protection of the brain. In this report, we find that loss of Gsk3β leads to a fully penetrant reduction of frontal bone size and subsequent enlarged frontal fontanelle. In the absence of Gsk3β the frontal bone primordium undergoes increased cell death and reduced proliferation with a concomitant increase in Fgfr2-IIIc and Twist1 expression. This leads to a smaller condensation and premature differentiation. This phenotype appears to be Wnt-independent and is not rescued by decreasing the genetic dose of β-catenin/Ctnnb1. Taken together, our work defines a novel role for Gsk3β in skull development.
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spelling pubmed-47575452016-02-26 Frontal Bone Insufficiency in Gsk3β Mutant Mice Szabo-Rogers, Heather Yakob, Wardati Liu, Karen J. PLoS One Research Article The development of the mammalian skull is a complex process that requires multiple tissue interactions and a balance of growth and differentiation. Disrupting this balance can lead to changes in the shape and size of skull bones, which can have serious clinical implications. For example, insufficient ossification of the bony elements leads to enlarged anterior fontanelles and reduced mechanical protection of the brain. In this report, we find that loss of Gsk3β leads to a fully penetrant reduction of frontal bone size and subsequent enlarged frontal fontanelle. In the absence of Gsk3β the frontal bone primordium undergoes increased cell death and reduced proliferation with a concomitant increase in Fgfr2-IIIc and Twist1 expression. This leads to a smaller condensation and premature differentiation. This phenotype appears to be Wnt-independent and is not rescued by decreasing the genetic dose of β-catenin/Ctnnb1. Taken together, our work defines a novel role for Gsk3β in skull development. Public Library of Science 2016-02-17 /pmc/articles/PMC4757545/ /pubmed/26886780 http://dx.doi.org/10.1371/journal.pone.0149604 Text en © 2016 Szabo-Rogers et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Szabo-Rogers, Heather
Yakob, Wardati
Liu, Karen J.
Frontal Bone Insufficiency in Gsk3β Mutant Mice
title Frontal Bone Insufficiency in Gsk3β Mutant Mice
title_full Frontal Bone Insufficiency in Gsk3β Mutant Mice
title_fullStr Frontal Bone Insufficiency in Gsk3β Mutant Mice
title_full_unstemmed Frontal Bone Insufficiency in Gsk3β Mutant Mice
title_short Frontal Bone Insufficiency in Gsk3β Mutant Mice
title_sort frontal bone insufficiency in gsk3β mutant mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757545/
https://www.ncbi.nlm.nih.gov/pubmed/26886780
http://dx.doi.org/10.1371/journal.pone.0149604
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