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High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level
The precise annotation and accurate identification of neural structures are prerequisites for studying mammalian brain function. The orientation of neurons and neural circuits is usually determined by mapping brain images to coarse axial-sampling planar reference atlases. However, individual differe...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932192/ https://www.ncbi.nlm.nih.gov/pubmed/27374071 http://dx.doi.org/10.1038/ncomms12142 |
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author | Gong, Hui Xu, Dongli Yuan, Jing Li, Xiangning Guo, Congdi Peng, Jie Li, Yuxin Schwarz, Lindsay A. Li, Anan Hu, Bihe Xiong, Benyi Sun, Qingtao Zhang, Yalun Liu, Jiepeng Zhong, Qiuyuan Xu, Tonghui Zeng, Shaoqun Luo, Qingming |
author_facet | Gong, Hui Xu, Dongli Yuan, Jing Li, Xiangning Guo, Congdi Peng, Jie Li, Yuxin Schwarz, Lindsay A. Li, Anan Hu, Bihe Xiong, Benyi Sun, Qingtao Zhang, Yalun Liu, Jiepeng Zhong, Qiuyuan Xu, Tonghui Zeng, Shaoqun Luo, Qingming |
author_sort | Gong, Hui |
collection | PubMed |
description | The precise annotation and accurate identification of neural structures are prerequisites for studying mammalian brain function. The orientation of neurons and neural circuits is usually determined by mapping brain images to coarse axial-sampling planar reference atlases. However, individual differences at the cellular level likely lead to position errors and an inability to orient neural projections at single-cell resolution. Here, we present a high-throughput precision imaging method that can acquire a co-localized brain-wide data set of both fluorescent-labelled neurons and counterstained cell bodies at a voxel size of 0.32 × 0.32 × 2.0 μm in 3 days for a single mouse brain. We acquire mouse whole-brain imaging data sets of multiple types of neurons and projections with anatomical annotation at single-neuron resolution. The results show that the simultaneous acquisition of labelled neural structures and cytoarchitecture reference in the same brain greatly facilitates precise tracing of long-range projections and accurate locating of nuclei. |
format | Online Article Text |
id | pubmed-4932192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49321922016-07-12 High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level Gong, Hui Xu, Dongli Yuan, Jing Li, Xiangning Guo, Congdi Peng, Jie Li, Yuxin Schwarz, Lindsay A. Li, Anan Hu, Bihe Xiong, Benyi Sun, Qingtao Zhang, Yalun Liu, Jiepeng Zhong, Qiuyuan Xu, Tonghui Zeng, Shaoqun Luo, Qingming Nat Commun Article The precise annotation and accurate identification of neural structures are prerequisites for studying mammalian brain function. The orientation of neurons and neural circuits is usually determined by mapping brain images to coarse axial-sampling planar reference atlases. However, individual differences at the cellular level likely lead to position errors and an inability to orient neural projections at single-cell resolution. Here, we present a high-throughput precision imaging method that can acquire a co-localized brain-wide data set of both fluorescent-labelled neurons and counterstained cell bodies at a voxel size of 0.32 × 0.32 × 2.0 μm in 3 days for a single mouse brain. We acquire mouse whole-brain imaging data sets of multiple types of neurons and projections with anatomical annotation at single-neuron resolution. The results show that the simultaneous acquisition of labelled neural structures and cytoarchitecture reference in the same brain greatly facilitates precise tracing of long-range projections and accurate locating of nuclei. Nature Publishing Group 2016-07-04 /pmc/articles/PMC4932192/ /pubmed/27374071 http://dx.doi.org/10.1038/ncomms12142 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ 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 Gong, Hui Xu, Dongli Yuan, Jing Li, Xiangning Guo, Congdi Peng, Jie Li, Yuxin Schwarz, Lindsay A. Li, Anan Hu, Bihe Xiong, Benyi Sun, Qingtao Zhang, Yalun Liu, Jiepeng Zhong, Qiuyuan Xu, Tonghui Zeng, Shaoqun Luo, Qingming High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level |
title | High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level |
title_full | High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level |
title_fullStr | High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level |
title_full_unstemmed | High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level |
title_short | High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level |
title_sort | high-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932192/ https://www.ncbi.nlm.nih.gov/pubmed/27374071 http://dx.doi.org/10.1038/ncomms12142 |
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