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Multimodal mapping of cell types and projections in the central nucleus of the amygdala
The central nucleus of the amygdala (CEA) is a brain region that integrates external and internal sensory information and executes innate and adaptive behaviors through distinct output pathways. Despite its complex functions, the diversity of molecularly defined neuronal types in the CEA and their c...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977318/ https://www.ncbi.nlm.nih.gov/pubmed/36661218 http://dx.doi.org/10.7554/eLife.84262 |
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author | Wang, Yuhan Krabbe, Sabine Eddison, Mark Henry, Fredrick E Fleishman, Greg Lemire, Andrew L Wang, Lihua Korff, Wyatt Tillberg, Paul W Lüthi, Andreas Sternson, Scott M |
author_facet | Wang, Yuhan Krabbe, Sabine Eddison, Mark Henry, Fredrick E Fleishman, Greg Lemire, Andrew L Wang, Lihua Korff, Wyatt Tillberg, Paul W Lüthi, Andreas Sternson, Scott M |
author_sort | Wang, Yuhan |
collection | PubMed |
description | The central nucleus of the amygdala (CEA) is a brain region that integrates external and internal sensory information and executes innate and adaptive behaviors through distinct output pathways. Despite its complex functions, the diversity of molecularly defined neuronal types in the CEA and their contributions to major axonal projection targets have not been examined systematically. Here, we performed single-cell RNA-sequencing (scRNA-seq) to classify molecularly defined cell types in the CEA and identified marker genes to map the location of these neuronal types using expansion-assisted iterative fluorescence in situ hybridization (EASI-FISH). We developed new methods to integrate EASI-FISH with 5-plex retrograde axonal labeling to determine the spatial, morphological, and connectivity properties of ~30,000 molecularly defined CEA neurons. Our study revealed spatiomolecular organization of the CEA, with medial and lateral CEA associated with distinct molecularly defined cell families. We also found a long-range axon projection network from the CEA, where target regions receive inputs from multiple molecularly defined cell types. Axon collateralization was found primarily among projections to hindbrain targets, which are distinct from forebrain projections. This resource reports marker gene combinations for molecularly defined cell types and axon-projection types, which will be useful for selective interrogation of these neuronal populations to study their contributions to the diverse functions of the CEA. |
format | Online Article Text |
id | pubmed-9977318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-99773182023-03-02 Multimodal mapping of cell types and projections in the central nucleus of the amygdala Wang, Yuhan Krabbe, Sabine Eddison, Mark Henry, Fredrick E Fleishman, Greg Lemire, Andrew L Wang, Lihua Korff, Wyatt Tillberg, Paul W Lüthi, Andreas Sternson, Scott M eLife Neuroscience The central nucleus of the amygdala (CEA) is a brain region that integrates external and internal sensory information and executes innate and adaptive behaviors through distinct output pathways. Despite its complex functions, the diversity of molecularly defined neuronal types in the CEA and their contributions to major axonal projection targets have not been examined systematically. Here, we performed single-cell RNA-sequencing (scRNA-seq) to classify molecularly defined cell types in the CEA and identified marker genes to map the location of these neuronal types using expansion-assisted iterative fluorescence in situ hybridization (EASI-FISH). We developed new methods to integrate EASI-FISH with 5-plex retrograde axonal labeling to determine the spatial, morphological, and connectivity properties of ~30,000 molecularly defined CEA neurons. Our study revealed spatiomolecular organization of the CEA, with medial and lateral CEA associated with distinct molecularly defined cell families. We also found a long-range axon projection network from the CEA, where target regions receive inputs from multiple molecularly defined cell types. Axon collateralization was found primarily among projections to hindbrain targets, which are distinct from forebrain projections. This resource reports marker gene combinations for molecularly defined cell types and axon-projection types, which will be useful for selective interrogation of these neuronal populations to study their contributions to the diverse functions of the CEA. eLife Sciences Publications, Ltd 2023-01-20 /pmc/articles/PMC9977318/ /pubmed/36661218 http://dx.doi.org/10.7554/eLife.84262 Text en © 2023, Wang et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Wang, Yuhan Krabbe, Sabine Eddison, Mark Henry, Fredrick E Fleishman, Greg Lemire, Andrew L Wang, Lihua Korff, Wyatt Tillberg, Paul W Lüthi, Andreas Sternson, Scott M Multimodal mapping of cell types and projections in the central nucleus of the amygdala |
title | Multimodal mapping of cell types and projections in the central nucleus of the amygdala |
title_full | Multimodal mapping of cell types and projections in the central nucleus of the amygdala |
title_fullStr | Multimodal mapping of cell types and projections in the central nucleus of the amygdala |
title_full_unstemmed | Multimodal mapping of cell types and projections in the central nucleus of the amygdala |
title_short | Multimodal mapping of cell types and projections in the central nucleus of the amygdala |
title_sort | multimodal mapping of cell types and projections in the central nucleus of the amygdala |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977318/ https://www.ncbi.nlm.nih.gov/pubmed/36661218 http://dx.doi.org/10.7554/eLife.84262 |
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