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A platform for efficient identification of molecular phenotypes of brain-wide neural circuits
A neural circuit is a structural-functional unit of achieving particular information transmission and processing, and have various inputs, outputs and molecular phenotypes. Systematic acquisition and comparative analysis of the molecular features of neural circuits are crucial to elucidating the ope...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654830/ https://www.ncbi.nlm.nih.gov/pubmed/29066836 http://dx.doi.org/10.1038/s41598-017-14360-6 |
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author | Jiang, Tao Long, Ben Gong, Hui Xu, Tonghui Li, Xiangning Duan, Zhuonan Li, Anan Deng, Lei Zhong, Qiuyuan Peng, Xue Yuan, Jing |
author_facet | Jiang, Tao Long, Ben Gong, Hui Xu, Tonghui Li, Xiangning Duan, Zhuonan Li, Anan Deng, Lei Zhong, Qiuyuan Peng, Xue Yuan, Jing |
author_sort | Jiang, Tao |
collection | PubMed |
description | A neural circuit is a structural-functional unit of achieving particular information transmission and processing, and have various inputs, outputs and molecular phenotypes. Systematic acquisition and comparative analysis of the molecular features of neural circuits are crucial to elucidating the operating mechanisms of brain function. However, no efficient, systematic approach is available for describing the molecular phenotypes of specific neural circuits at the whole brain scale. In this study, we developed a rapid whole-brain optical tomography method and devised an efficient approach to map brain-wide structural and molecular information in the same brain: rapidly imaging and sectioning the whole brain as well as automatically collecting all slices; conveniently selecting slices of interest through quick data browsing and then performing post hoc immunostaining of selected slices. Using this platform, we mapped the brain-wide distribution of inputs to motor, sensory and visual cortices and determined their molecular phenotypes in several subcortical regions. Our platform significantly enhances the efficiency of molecular phenotyping of neural circuits and provides access to automation and industrialization of cell type analyses for specific circuits. |
format | Online Article Text |
id | pubmed-5654830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56548302017-10-31 A platform for efficient identification of molecular phenotypes of brain-wide neural circuits Jiang, Tao Long, Ben Gong, Hui Xu, Tonghui Li, Xiangning Duan, Zhuonan Li, Anan Deng, Lei Zhong, Qiuyuan Peng, Xue Yuan, Jing Sci Rep Article A neural circuit is a structural-functional unit of achieving particular information transmission and processing, and have various inputs, outputs and molecular phenotypes. Systematic acquisition and comparative analysis of the molecular features of neural circuits are crucial to elucidating the operating mechanisms of brain function. However, no efficient, systematic approach is available for describing the molecular phenotypes of specific neural circuits at the whole brain scale. In this study, we developed a rapid whole-brain optical tomography method and devised an efficient approach to map brain-wide structural and molecular information in the same brain: rapidly imaging and sectioning the whole brain as well as automatically collecting all slices; conveniently selecting slices of interest through quick data browsing and then performing post hoc immunostaining of selected slices. Using this platform, we mapped the brain-wide distribution of inputs to motor, sensory and visual cortices and determined their molecular phenotypes in several subcortical regions. Our platform significantly enhances the efficiency of molecular phenotyping of neural circuits and provides access to automation and industrialization of cell type analyses for specific circuits. Nature Publishing Group UK 2017-10-24 /pmc/articles/PMC5654830/ /pubmed/29066836 http://dx.doi.org/10.1038/s41598-017-14360-6 Text en © The Author(s) 2017 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 Jiang, Tao Long, Ben Gong, Hui Xu, Tonghui Li, Xiangning Duan, Zhuonan Li, Anan Deng, Lei Zhong, Qiuyuan Peng, Xue Yuan, Jing A platform for efficient identification of molecular phenotypes of brain-wide neural circuits |
title | A platform for efficient identification of molecular phenotypes of brain-wide neural circuits |
title_full | A platform for efficient identification of molecular phenotypes of brain-wide neural circuits |
title_fullStr | A platform for efficient identification of molecular phenotypes of brain-wide neural circuits |
title_full_unstemmed | A platform for efficient identification of molecular phenotypes of brain-wide neural circuits |
title_short | A platform for efficient identification of molecular phenotypes of brain-wide neural circuits |
title_sort | platform for efficient identification of molecular phenotypes of brain-wide neural circuits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654830/ https://www.ncbi.nlm.nih.gov/pubmed/29066836 http://dx.doi.org/10.1038/s41598-017-14360-6 |
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