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Light microscopy based approach for mapping connectivity with molecular specificity
Mapping neuroanatomy is a foundational goal towards understanding brain function. Electron microscopy (EM) has been the gold standard for connectivity analysis because nanoscale resolution is necessary to unambiguously resolve synapses. However, molecular information that specifies cell types is oft...
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/PMC7493953/ https://www.ncbi.nlm.nih.gov/pubmed/32934230 http://dx.doi.org/10.1038/s41467-020-18422-8 |
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author | Shen, Fred Y. Harrington, Margaret M. Walker, Logan A. Cheng, Hon Pong Jimmy Boyden, Edward S. Cai, Dawen |
author_facet | Shen, Fred Y. Harrington, Margaret M. Walker, Logan A. Cheng, Hon Pong Jimmy Boyden, Edward S. Cai, Dawen |
author_sort | Shen, Fred Y. |
collection | PubMed |
description | Mapping neuroanatomy is a foundational goal towards understanding brain function. Electron microscopy (EM) has been the gold standard for connectivity analysis because nanoscale resolution is necessary to unambiguously resolve synapses. However, molecular information that specifies cell types is often lost in EM reconstructions. To address this, we devise a light microscopy approach for connectivity analysis of defined cell types called spectral connectomics. We combine multicolor labeling (Brainbow) of neurons with multi-round immunostaining Expansion Microscopy (miriEx) to simultaneously interrogate morphology, molecular markers, and connectivity in the same brain section. We apply this strategy to directly link inhibitory neuron cell types with their morphologies. Furthermore, we show that correlative Brainbow and endogenous synaptic machinery immunostaining can define putative synaptic connections between neurons, as well as map putative inhibitory and excitatory inputs. We envision that spectral connectomics can be applied routinely in neurobiology labs to gain insights into normal and pathophysiological neuroanatomy. |
format | Online Article Text |
id | pubmed-7493953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74939532020-10-01 Light microscopy based approach for mapping connectivity with molecular specificity Shen, Fred Y. Harrington, Margaret M. Walker, Logan A. Cheng, Hon Pong Jimmy Boyden, Edward S. Cai, Dawen Nat Commun Article Mapping neuroanatomy is a foundational goal towards understanding brain function. Electron microscopy (EM) has been the gold standard for connectivity analysis because nanoscale resolution is necessary to unambiguously resolve synapses. However, molecular information that specifies cell types is often lost in EM reconstructions. To address this, we devise a light microscopy approach for connectivity analysis of defined cell types called spectral connectomics. We combine multicolor labeling (Brainbow) of neurons with multi-round immunostaining Expansion Microscopy (miriEx) to simultaneously interrogate morphology, molecular markers, and connectivity in the same brain section. We apply this strategy to directly link inhibitory neuron cell types with their morphologies. Furthermore, we show that correlative Brainbow and endogenous synaptic machinery immunostaining can define putative synaptic connections between neurons, as well as map putative inhibitory and excitatory inputs. We envision that spectral connectomics can be applied routinely in neurobiology labs to gain insights into normal and pathophysiological neuroanatomy. Nature Publishing Group UK 2020-09-15 /pmc/articles/PMC7493953/ /pubmed/32934230 http://dx.doi.org/10.1038/s41467-020-18422-8 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 Shen, Fred Y. Harrington, Margaret M. Walker, Logan A. Cheng, Hon Pong Jimmy Boyden, Edward S. Cai, Dawen Light microscopy based approach for mapping connectivity with molecular specificity |
title | Light microscopy based approach for mapping connectivity with molecular specificity |
title_full | Light microscopy based approach for mapping connectivity with molecular specificity |
title_fullStr | Light microscopy based approach for mapping connectivity with molecular specificity |
title_full_unstemmed | Light microscopy based approach for mapping connectivity with molecular specificity |
title_short | Light microscopy based approach for mapping connectivity with molecular specificity |
title_sort | light microscopy based approach for mapping connectivity with molecular specificity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493953/ https://www.ncbi.nlm.nih.gov/pubmed/32934230 http://dx.doi.org/10.1038/s41467-020-18422-8 |
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