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Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape

Canonical Wnt signaling plays multiple roles critical to normal craniofacial development while its dysregulation is known to be involved in structural birth defects of the face. However, when and how Wnt signaling influences phenotypic variation, including those associated with disease, remains uncl...

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Autores principales: Marchini, Marta, Hu, Diane, Lo Vercio, Lucas, Young, Nathan M., Forkert, Nils D., Hallgrímsson, Benedikt, Marcucio, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8039397/
https://www.ncbi.nlm.nih.gov/pubmed/33855022
http://dx.doi.org/10.3389/fcell.2021.644099
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author Marchini, Marta
Hu, Diane
Lo Vercio, Lucas
Young, Nathan M.
Forkert, Nils D.
Hallgrímsson, Benedikt
Marcucio, Ralph
author_facet Marchini, Marta
Hu, Diane
Lo Vercio, Lucas
Young, Nathan M.
Forkert, Nils D.
Hallgrímsson, Benedikt
Marcucio, Ralph
author_sort Marchini, Marta
collection PubMed
description Canonical Wnt signaling plays multiple roles critical to normal craniofacial development while its dysregulation is known to be involved in structural birth defects of the face. However, when and how Wnt signaling influences phenotypic variation, including those associated with disease, remains unclear. One potential mechanism is via Wnt signaling’s role in the patterning of an early facial signaling center, the frontonasal ectodermal zone (FEZ), and its subsequent regulation of early facial morphogenesis. For example, Wnt signaling may directly alter the shape and/or magnitude of expression of the sonic hedgehog (SHH) domain in the FEZ. To test this idea, we used a replication-competent avian sarcoma retrovirus (RCAS) encoding Wnt3a to modulate its expression in the facial mesenchyme. We then quantified and compared ontogenetic changes in treated to untreated embryos in the three-dimensional (3D) shape of both the SHH expression domain of the FEZ, and the morphology of the facial primordia and brain using iodine-contrast microcomputed tomography imaging and 3D geometric morphometrics (3DGM). We found that increased Wnt3a expression in early stages of head development produces correlated variation in shape between both structural and signaling levels of analysis. In addition, altered Wnt3a activation disrupted the integration between the forebrain and other neural tube derivatives. These results show that activation of Wnt signaling influences facial shape through its impact on the forebrain and SHH expression in the FEZ, and highlights the close relationship between morphogenesis of the forebrain and midface.
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spelling pubmed-80393972021-04-13 Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape Marchini, Marta Hu, Diane Lo Vercio, Lucas Young, Nathan M. Forkert, Nils D. Hallgrímsson, Benedikt Marcucio, Ralph Front Cell Dev Biol Cell and Developmental Biology Canonical Wnt signaling plays multiple roles critical to normal craniofacial development while its dysregulation is known to be involved in structural birth defects of the face. However, when and how Wnt signaling influences phenotypic variation, including those associated with disease, remains unclear. One potential mechanism is via Wnt signaling’s role in the patterning of an early facial signaling center, the frontonasal ectodermal zone (FEZ), and its subsequent regulation of early facial morphogenesis. For example, Wnt signaling may directly alter the shape and/or magnitude of expression of the sonic hedgehog (SHH) domain in the FEZ. To test this idea, we used a replication-competent avian sarcoma retrovirus (RCAS) encoding Wnt3a to modulate its expression in the facial mesenchyme. We then quantified and compared ontogenetic changes in treated to untreated embryos in the three-dimensional (3D) shape of both the SHH expression domain of the FEZ, and the morphology of the facial primordia and brain using iodine-contrast microcomputed tomography imaging and 3D geometric morphometrics (3DGM). We found that increased Wnt3a expression in early stages of head development produces correlated variation in shape between both structural and signaling levels of analysis. In addition, altered Wnt3a activation disrupted the integration between the forebrain and other neural tube derivatives. These results show that activation of Wnt signaling influences facial shape through its impact on the forebrain and SHH expression in the FEZ, and highlights the close relationship between morphogenesis of the forebrain and midface. Frontiers Media S.A. 2021-03-29 /pmc/articles/PMC8039397/ /pubmed/33855022 http://dx.doi.org/10.3389/fcell.2021.644099 Text en Copyright © 2021 Marchini, Hu, Lo Vercio, Young, Forkert, Hallgrímsson and Marcucio. 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
Marchini, Marta
Hu, Diane
Lo Vercio, Lucas
Young, Nathan M.
Forkert, Nils D.
Hallgrímsson, Benedikt
Marcucio, Ralph
Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape
title Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape
title_full Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape
title_fullStr Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape
title_full_unstemmed Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape
title_short Wnt Signaling Drives Correlated Changes in Facial Morphology and Brain Shape
title_sort wnt signaling drives correlated changes in facial morphology and brain shape
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8039397/
https://www.ncbi.nlm.nih.gov/pubmed/33855022
http://dx.doi.org/10.3389/fcell.2021.644099
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