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Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains
The oxytocin receptor (OTR) plays critical roles in social behavior development. Despite its significance, brain-wide quantitative understanding of OTR expression remains limited in postnatally developing brains. Here, we develop postnatal 3D template brains to register whole brain images with cellu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171089/ https://www.ncbi.nlm.nih.gov/pubmed/32313029 http://dx.doi.org/10.1038/s41467-020-15659-1 |
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author | Newmaster, Kyra T. Nolan, Zachary T. Chon, Uree Vanselow, Daniel J. Weit, Abigael R. Tabbaa, Manal Hidema, Shizu Nishimori, Katsuhiko Hammock, Elizabeth A. D. Kim, Yongsoo |
author_facet | Newmaster, Kyra T. Nolan, Zachary T. Chon, Uree Vanselow, Daniel J. Weit, Abigael R. Tabbaa, Manal Hidema, Shizu Nishimori, Katsuhiko Hammock, Elizabeth A. D. Kim, Yongsoo |
author_sort | Newmaster, Kyra T. |
collection | PubMed |
description | The oxytocin receptor (OTR) plays critical roles in social behavior development. Despite its significance, brain-wide quantitative understanding of OTR expression remains limited in postnatally developing brains. Here, we develop postnatal 3D template brains to register whole brain images with cellular resolution to systematically quantify OTR cell densities. We utilize fluorescent reporter mice (Otr(venus/+)) and find that cortical regions show temporally and spatially heterogeneous patterns with transient postnatal OTR expression without cell death. Cortical OTR cells are largely glutamatergic neurons with the exception of cells in layer 6b. Subcortical regions show similar temporal regulation except the hypothalamus and two hypothalamic nuclei display sexually dimorphic OTR expression. Lack of OTR expression correlates with reduced dendritic spine densities in selected cortical regions of developing brains. Lastly, we create a website to visualize our high-resolution imaging data. In summary, our research provides a comprehensive resource for postnatal OTR expression in the mouse brain. |
format | Online Article Text |
id | pubmed-7171089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71710892020-04-23 Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains Newmaster, Kyra T. Nolan, Zachary T. Chon, Uree Vanselow, Daniel J. Weit, Abigael R. Tabbaa, Manal Hidema, Shizu Nishimori, Katsuhiko Hammock, Elizabeth A. D. Kim, Yongsoo Nat Commun Article The oxytocin receptor (OTR) plays critical roles in social behavior development. Despite its significance, brain-wide quantitative understanding of OTR expression remains limited in postnatally developing brains. Here, we develop postnatal 3D template brains to register whole brain images with cellular resolution to systematically quantify OTR cell densities. We utilize fluorescent reporter mice (Otr(venus/+)) and find that cortical regions show temporally and spatially heterogeneous patterns with transient postnatal OTR expression without cell death. Cortical OTR cells are largely glutamatergic neurons with the exception of cells in layer 6b. Subcortical regions show similar temporal regulation except the hypothalamus and two hypothalamic nuclei display sexually dimorphic OTR expression. Lack of OTR expression correlates with reduced dendritic spine densities in selected cortical regions of developing brains. Lastly, we create a website to visualize our high-resolution imaging data. In summary, our research provides a comprehensive resource for postnatal OTR expression in the mouse brain. Nature Publishing Group UK 2020-04-20 /pmc/articles/PMC7171089/ /pubmed/32313029 http://dx.doi.org/10.1038/s41467-020-15659-1 Text en © The Author(s) 2020 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 Newmaster, Kyra T. Nolan, Zachary T. Chon, Uree Vanselow, Daniel J. Weit, Abigael R. Tabbaa, Manal Hidema, Shizu Nishimori, Katsuhiko Hammock, Elizabeth A. D. Kim, Yongsoo Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains |
title | Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains |
title_full | Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains |
title_fullStr | Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains |
title_full_unstemmed | Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains |
title_short | Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains |
title_sort | quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171089/ https://www.ncbi.nlm.nih.gov/pubmed/32313029 http://dx.doi.org/10.1038/s41467-020-15659-1 |
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