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Pten haploinsufficiency disrupts scaling across brain areas during development in mice

Haploinsufficiency for PTEN is a cause of autism spectrum disorder and brain overgrowth; however, it is not known if PTEN mutations disrupt scaling across brain areas during development. To address this question, we used magnetic resonance imaging to analyze brains of male Pten haploinsufficient (Pt...

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Autores principales: Clipperton-Allen, Amy E., Cohen, Ori S., Aceti, Massimiliano, Zucca, Aya, Levy, Jenna, Ellegood, Jacob, Lerch, Jason P., Page, Damon T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895202/
https://www.ncbi.nlm.nih.gov/pubmed/31804455
http://dx.doi.org/10.1038/s41398-019-0656-6
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author Clipperton-Allen, Amy E.
Cohen, Ori S.
Aceti, Massimiliano
Zucca, Aya
Levy, Jenna
Ellegood, Jacob
Lerch, Jason P.
Page, Damon T.
author_facet Clipperton-Allen, Amy E.
Cohen, Ori S.
Aceti, Massimiliano
Zucca, Aya
Levy, Jenna
Ellegood, Jacob
Lerch, Jason P.
Page, Damon T.
author_sort Clipperton-Allen, Amy E.
collection PubMed
description Haploinsufficiency for PTEN is a cause of autism spectrum disorder and brain overgrowth; however, it is not known if PTEN mutations disrupt scaling across brain areas during development. To address this question, we used magnetic resonance imaging to analyze brains of male Pten haploinsufficient (Pten(+/−)) mice and wild-type littermates during early postnatal development and adulthood. Adult Pten(+/−) mice display a consistent pattern of abnormal scaling across brain areas, with white matter (WM) areas being particularly affected. This regional and WM enlargement recapitulates structural abnormalities found in individuals with PTEN haploinsufficiency and autism. Early postnatal Pten(+/−) mice do not display the same pattern, instead exhibiting greater variability across mice and brain regions than controls. This suggests that Pten haploinsufficiency may desynchronize growth across brain regions during early development before stabilizing by maturity. Pten(+/−) cortical cultures display increased proliferation of glial cell populations, indicating a potential substrate of WM enlargement, and provide a platform for testing candidate therapeutics. Pten haploinsufficiency dysregulates coordinated growth across brain regions during development. This results in abnormally scaled brain areas and associated behavioral deficits, potentially explaining the relationship between PTEN mutations and neurodevelopmental disorders.
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spelling pubmed-68952022019-12-13 Pten haploinsufficiency disrupts scaling across brain areas during development in mice Clipperton-Allen, Amy E. Cohen, Ori S. Aceti, Massimiliano Zucca, Aya Levy, Jenna Ellegood, Jacob Lerch, Jason P. Page, Damon T. Transl Psychiatry Article Haploinsufficiency for PTEN is a cause of autism spectrum disorder and brain overgrowth; however, it is not known if PTEN mutations disrupt scaling across brain areas during development. To address this question, we used magnetic resonance imaging to analyze brains of male Pten haploinsufficient (Pten(+/−)) mice and wild-type littermates during early postnatal development and adulthood. Adult Pten(+/−) mice display a consistent pattern of abnormal scaling across brain areas, with white matter (WM) areas being particularly affected. This regional and WM enlargement recapitulates structural abnormalities found in individuals with PTEN haploinsufficiency and autism. Early postnatal Pten(+/−) mice do not display the same pattern, instead exhibiting greater variability across mice and brain regions than controls. This suggests that Pten haploinsufficiency may desynchronize growth across brain regions during early development before stabilizing by maturity. Pten(+/−) cortical cultures display increased proliferation of glial cell populations, indicating a potential substrate of WM enlargement, and provide a platform for testing candidate therapeutics. Pten haploinsufficiency dysregulates coordinated growth across brain regions during development. This results in abnormally scaled brain areas and associated behavioral deficits, potentially explaining the relationship between PTEN mutations and neurodevelopmental disorders. Nature Publishing Group UK 2019-12-05 /pmc/articles/PMC6895202/ /pubmed/31804455 http://dx.doi.org/10.1038/s41398-019-0656-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Clipperton-Allen, Amy E.
Cohen, Ori S.
Aceti, Massimiliano
Zucca, Aya
Levy, Jenna
Ellegood, Jacob
Lerch, Jason P.
Page, Damon T.
Pten haploinsufficiency disrupts scaling across brain areas during development in mice
title Pten haploinsufficiency disrupts scaling across brain areas during development in mice
title_full Pten haploinsufficiency disrupts scaling across brain areas during development in mice
title_fullStr Pten haploinsufficiency disrupts scaling across brain areas during development in mice
title_full_unstemmed Pten haploinsufficiency disrupts scaling across brain areas during development in mice
title_short Pten haploinsufficiency disrupts scaling across brain areas during development in mice
title_sort pten haploinsufficiency disrupts scaling across brain areas during development in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895202/
https://www.ncbi.nlm.nih.gov/pubmed/31804455
http://dx.doi.org/10.1038/s41398-019-0656-6
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