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In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain
Hundreds of inbred mouse strains are established for use in a broad spectrum of basic research fields, including genetics, neuroscience, immunology, and cancer. Inbred mice exhibit identical intra-strain genetics and divergent inter-strain phenotypes. The cognitive and behavioral divergences must be...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427914/ https://www.ncbi.nlm.nih.gov/pubmed/28273899 http://dx.doi.org/10.1038/s41598-017-00148-1 |
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author | Hikishima, Keigo Komaki, Yuji Seki, Fumiko Ohnishi, Yasuyuki Okano, Hirotaka J. Okano, Hideyuki |
author_facet | Hikishima, Keigo Komaki, Yuji Seki, Fumiko Ohnishi, Yasuyuki Okano, Hirotaka J. Okano, Hideyuki |
author_sort | Hikishima, Keigo |
collection | PubMed |
description | Hundreds of inbred mouse strains are established for use in a broad spectrum of basic research fields, including genetics, neuroscience, immunology, and cancer. Inbred mice exhibit identical intra-strain genetics and divergent inter-strain phenotypes. The cognitive and behavioral divergences must be controlled by the variances of structure and function of their brains; however, the underlying morphological features of strain-to-strain difference remain obscure. Here, in vivo microscopic magnetic resonance imaging was optimized to image the mouse brains by using an isotropic resolution of 80 μm. Next, in vivo templates were created from the data from four major inbred mouse strains (C57Bl/6, BALB/cBy, C3H/He, and DBA/2). A strain-mixed brain template was also created, and the template was then employed to establish automatic voxel-based morphometry (VBM) for the mouse brain. The VBM assessment revealed strain-specific brain morphologies concerning the gray matter volume of the four strains, with a smaller volume in the primary visual cortex for the C3H/He strain, and a smaller volume in the primary auditory cortex and field CA1 of the hippocampus for the DBA/2 strain. These findings would contribute to the basis of for understanding morphological phenotype of the inbred mouse strain and may indicate a relationship between brain morphology and strain-specific cognition and behavior. |
format | Online Article Text |
id | pubmed-5427914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54279142017-05-12 In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain Hikishima, Keigo Komaki, Yuji Seki, Fumiko Ohnishi, Yasuyuki Okano, Hirotaka J. Okano, Hideyuki Sci Rep Article Hundreds of inbred mouse strains are established for use in a broad spectrum of basic research fields, including genetics, neuroscience, immunology, and cancer. Inbred mice exhibit identical intra-strain genetics and divergent inter-strain phenotypes. The cognitive and behavioral divergences must be controlled by the variances of structure and function of their brains; however, the underlying morphological features of strain-to-strain difference remain obscure. Here, in vivo microscopic magnetic resonance imaging was optimized to image the mouse brains by using an isotropic resolution of 80 μm. Next, in vivo templates were created from the data from four major inbred mouse strains (C57Bl/6, BALB/cBy, C3H/He, and DBA/2). A strain-mixed brain template was also created, and the template was then employed to establish automatic voxel-based morphometry (VBM) for the mouse brain. The VBM assessment revealed strain-specific brain morphologies concerning the gray matter volume of the four strains, with a smaller volume in the primary visual cortex for the C3H/He strain, and a smaller volume in the primary auditory cortex and field CA1 of the hippocampus for the DBA/2 strain. These findings would contribute to the basis of for understanding morphological phenotype of the inbred mouse strain and may indicate a relationship between brain morphology and strain-specific cognition and behavior. Nature Publishing Group UK 2017-03-07 /pmc/articles/PMC5427914/ /pubmed/28273899 http://dx.doi.org/10.1038/s41598-017-00148-1 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hikishima, Keigo Komaki, Yuji Seki, Fumiko Ohnishi, Yasuyuki Okano, Hirotaka J. Okano, Hideyuki In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain |
title | In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain |
title_full | In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain |
title_fullStr | In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain |
title_full_unstemmed | In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain |
title_short | In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain |
title_sort | in vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427914/ https://www.ncbi.nlm.nih.gov/pubmed/28273899 http://dx.doi.org/10.1038/s41598-017-00148-1 |
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