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Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy
OBJECTIVE: Autism spectrum disorder (ASD) encompasses a group of neurodevelopmental conditions that remain poorly understood due to their genetic complexity. CHD8 is a risk allele strongly associated with ASD, and heterozygous Chd8 loss-of-function mice have been reported to exhibit macrocephaly in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802325/ https://www.ncbi.nlm.nih.gov/pubmed/33436073 http://dx.doi.org/10.1186/s13104-020-05436-0 |
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author | Gómez, Harold F. Hodel, Leonie Michos, Odyssé Iber, Dagmar |
author_facet | Gómez, Harold F. Hodel, Leonie Michos, Odyssé Iber, Dagmar |
author_sort | Gómez, Harold F. |
collection | PubMed |
description | OBJECTIVE: Autism spectrum disorder (ASD) encompasses a group of neurodevelopmental conditions that remain poorly understood due to their genetic complexity. CHD8 is a risk allele strongly associated with ASD, and heterozygous Chd8 loss-of-function mice have been reported to exhibit macrocephaly in early postnatal stages. In this work, we sought to identify measurable brain alterations in early embryonic development. RESULTS: We performed light-sheet fluorescence microscopy imaging of N-cadherin stained and optically cleared Chd8(+/−) and wild-type mouse brains at embryonic day 12.5 (E12.5). We report a detailed morphometric characterization of embryonic brain shapes and cortical neuroepithelial apical architecture. While Chd8(+/−) characteristic expansion of the forebrain and midbrain was not observed this early in embryogenesis, a tendency for a decreased lateral ventricular sphericity and an increased intraocular distance in Chd8(+/−) brains was found compared to controls. This study advocates the use of high-resolution microscopy technologies and multi-scale morphometric analyses of target brain regions to explore the etiology and cellular basis of Chd8 haploinsufficiency. |
format | Online Article Text |
id | pubmed-7802325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78023252021-01-13 Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy Gómez, Harold F. Hodel, Leonie Michos, Odyssé Iber, Dagmar BMC Res Notes Research Note OBJECTIVE: Autism spectrum disorder (ASD) encompasses a group of neurodevelopmental conditions that remain poorly understood due to their genetic complexity. CHD8 is a risk allele strongly associated with ASD, and heterozygous Chd8 loss-of-function mice have been reported to exhibit macrocephaly in early postnatal stages. In this work, we sought to identify measurable brain alterations in early embryonic development. RESULTS: We performed light-sheet fluorescence microscopy imaging of N-cadherin stained and optically cleared Chd8(+/−) and wild-type mouse brains at embryonic day 12.5 (E12.5). We report a detailed morphometric characterization of embryonic brain shapes and cortical neuroepithelial apical architecture. While Chd8(+/−) characteristic expansion of the forebrain and midbrain was not observed this early in embryogenesis, a tendency for a decreased lateral ventricular sphericity and an increased intraocular distance in Chd8(+/−) brains was found compared to controls. This study advocates the use of high-resolution microscopy technologies and multi-scale morphometric analyses of target brain regions to explore the etiology and cellular basis of Chd8 haploinsufficiency. BioMed Central 2021-01-12 /pmc/articles/PMC7802325/ /pubmed/33436073 http://dx.doi.org/10.1186/s13104-020-05436-0 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Note Gómez, Harold F. Hodel, Leonie Michos, Odyssé Iber, Dagmar Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy |
title | Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy |
title_full | Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy |
title_fullStr | Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy |
title_full_unstemmed | Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy |
title_short | Morphological study of embryonic Chd8(+/−) mouse brains using light-sheet microscopy |
title_sort | morphological study of embryonic chd8(+/−) mouse brains using light-sheet microscopy |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802325/ https://www.ncbi.nlm.nih.gov/pubmed/33436073 http://dx.doi.org/10.1186/s13104-020-05436-0 |
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