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Unique functional responses differentially map onto genetic subtypes of dopamine neurons
Dopamine neurons are characterized by their response to unexpected rewards, but they also fire during movement and aversive stimuli. Dopamine neuron diversity has been observed based on molecular expression profiles; however, whether different functions map onto such genetic subtypes remains unclear...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545540/ https://www.ncbi.nlm.nih.gov/pubmed/37537242 http://dx.doi.org/10.1038/s41593-023-01401-9 |
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author | Azcorra, Maite Gaertner, Zachary Davidson, Connor He, Qianzi Kim, Hailey Nagappan, Shivathmihai Hayes, Cooper K. Ramakrishnan, Charu Fenno, Lief Kim, Yoon Seok Deisseroth, Karl Longnecker, Richard Awatramani, Rajeshwar Dombeck, Daniel A. |
author_facet | Azcorra, Maite Gaertner, Zachary Davidson, Connor He, Qianzi Kim, Hailey Nagappan, Shivathmihai Hayes, Cooper K. Ramakrishnan, Charu Fenno, Lief Kim, Yoon Seok Deisseroth, Karl Longnecker, Richard Awatramani, Rajeshwar Dombeck, Daniel A. |
author_sort | Azcorra, Maite |
collection | PubMed |
description | Dopamine neurons are characterized by their response to unexpected rewards, but they also fire during movement and aversive stimuli. Dopamine neuron diversity has been observed based on molecular expression profiles; however, whether different functions map onto such genetic subtypes remains unclear. In this study, we established that three genetic dopamine neuron subtypes within the substantia nigra pars compacta, characterized by the expression of Slc17a6 (Vglut2), Calb1 and Anxa1, each have a unique set of responses to rewards, aversive stimuli and accelerations and decelerations, and these signaling patterns are highly correlated between somas and axons within subtypes. Remarkably, reward responses were almost entirely absent in the Anxa1(+) subtype, which instead displayed acceleration-correlated signaling. Our findings establish a connection between functional and genetic dopamine neuron subtypes and demonstrate that molecular expression patterns can serve as a common framework to dissect dopaminergic functions. |
format | Online Article Text |
id | pubmed-10545540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-105455402023-10-04 Unique functional responses differentially map onto genetic subtypes of dopamine neurons Azcorra, Maite Gaertner, Zachary Davidson, Connor He, Qianzi Kim, Hailey Nagappan, Shivathmihai Hayes, Cooper K. Ramakrishnan, Charu Fenno, Lief Kim, Yoon Seok Deisseroth, Karl Longnecker, Richard Awatramani, Rajeshwar Dombeck, Daniel A. Nat Neurosci Article Dopamine neurons are characterized by their response to unexpected rewards, but they also fire during movement and aversive stimuli. Dopamine neuron diversity has been observed based on molecular expression profiles; however, whether different functions map onto such genetic subtypes remains unclear. In this study, we established that three genetic dopamine neuron subtypes within the substantia nigra pars compacta, characterized by the expression of Slc17a6 (Vglut2), Calb1 and Anxa1, each have a unique set of responses to rewards, aversive stimuli and accelerations and decelerations, and these signaling patterns are highly correlated between somas and axons within subtypes. Remarkably, reward responses were almost entirely absent in the Anxa1(+) subtype, which instead displayed acceleration-correlated signaling. Our findings establish a connection between functional and genetic dopamine neuron subtypes and demonstrate that molecular expression patterns can serve as a common framework to dissect dopaminergic functions. Nature Publishing Group US 2023-08-03 2023 /pmc/articles/PMC10545540/ /pubmed/37537242 http://dx.doi.org/10.1038/s41593-023-01401-9 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Azcorra, Maite Gaertner, Zachary Davidson, Connor He, Qianzi Kim, Hailey Nagappan, Shivathmihai Hayes, Cooper K. Ramakrishnan, Charu Fenno, Lief Kim, Yoon Seok Deisseroth, Karl Longnecker, Richard Awatramani, Rajeshwar Dombeck, Daniel A. Unique functional responses differentially map onto genetic subtypes of dopamine neurons |
title | Unique functional responses differentially map onto genetic subtypes of dopamine neurons |
title_full | Unique functional responses differentially map onto genetic subtypes of dopamine neurons |
title_fullStr | Unique functional responses differentially map onto genetic subtypes of dopamine neurons |
title_full_unstemmed | Unique functional responses differentially map onto genetic subtypes of dopamine neurons |
title_short | Unique functional responses differentially map onto genetic subtypes of dopamine neurons |
title_sort | unique functional responses differentially map onto genetic subtypes of dopamine neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545540/ https://www.ncbi.nlm.nih.gov/pubmed/37537242 http://dx.doi.org/10.1038/s41593-023-01401-9 |
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