Abstract

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.

The authors establish a connection between functional subtypes and genetic subtypes of dopamine neurons in mice and demonstrate that molecular expression patterns can serve as a common framework to dissect dopaminergic functions.

Details

Title
Unique functional responses differentially map onto genetic subtypes of dopamine neurons
Author
Azcorra, Maite 1   VIAFID ORCID Logo  ; Gaertner, Zachary 2   VIAFID ORCID Logo  ; Davidson, Connor 3 ; He, Qianzi 3 ; Kim, Hailey 4 ; Nagappan, Shivathmihai 3 ; Hayes, Cooper K. 5   VIAFID ORCID Logo  ; Ramakrishnan, Charu 6   VIAFID ORCID Logo  ; Fenno, Lief 7   VIAFID ORCID Logo  ; Kim, Yoon Seok 6 ; Deisseroth, Karl 6   VIAFID ORCID Logo  ; Longnecker, Richard 5 ; Awatramani, Rajeshwar 2   VIAFID ORCID Logo  ; Dombeck, Daniel A. 3   VIAFID ORCID Logo 

 Northwestern University, Department of Neurobiology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Department of Neurology, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, USA (GRID:grid.513948.2) (ISNI:0000 0005 0380 6410) 
 Northwestern University, Department of Neurology, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, USA (GRID:grid.513948.2) (ISNI:0000 0005 0380 6410) 
 Northwestern University, Department of Neurobiology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, USA (GRID:grid.513948.2) (ISNI:0000 0005 0380 6410) 
 Northwestern University, Department of Neurobiology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507) 
 Northwestern University, Department of Microbiology and Immunology, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507) 
 Stanford University School of Medicine, Department of Bioengineering, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956) 
 Stanford University School of Medicine, Department of Bioengineering, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956); The University of Texas at Austin, Departments of Neuroscience & Psychiatry, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924) 
Pages
1762-1774
Publication year
2023
Publication date
Oct 2023
Publisher
Nature Publishing Group
ISSN
10976256
e-ISSN
15461726
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2871492484
Copyright
© The Author(s) 2023. corrected publication 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.