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Dopamine-sensitive neurons in the mesencephalic locomotor region control locomotion initiation, stop, and turns.

Authors :
Juárez Tello A
van der Zouwen CI
Dejas L
Duque-Yate J
Boutin J
Medina-Ortiz K
Suresh JS
Swiegers J
Sarret P
Ryczko D
Source :
Cell reports [Cell Rep] 2024 May 28; Vol. 43 (5), pp. 114187. Date of Electronic Publication: 2024 May 08.
Publication Year :
2024

Abstract

The locomotor role of dopaminergic neurons is traditionally attributed to their ascending projections to the basal ganglia, which project to the mesencephalic locomotor region (MLR). In addition, descending dopaminergic projections to the MLR are present from basal vertebrates to mammals. However, the neurons targeted in the MLR and their behavioral role are unknown in mammals. Here, we identify genetically defined MLR cells that express D <subscript>1</subscript> or D <subscript>2</subscript> receptors and control different motor behaviors in mice. In the cuneiform nucleus, D <subscript>1</subscript> -expressing neurons promote locomotion, while D <subscript>2</subscript> -expressing neurons stop locomotion. In the pedunculopontine nucleus, D <subscript>1</subscript> -expressing neurons promote locomotion, while D <subscript>2</subscript> -expressing neurons evoke ipsilateral turns. Using RNAscope, we show that MLR dopamine-sensitive neurons comprise a combination of glutamatergic, GABAergic, and cholinergic neurons, suggesting that different neurotransmitter-based cell types work together to control distinct behavioral modules. Altogether, our study uncovers behaviorally relevant cell types in the mammalian MLR based on the expression of dopaminergic receptors.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2211-1247
Volume :
43
Issue :
5
Database :
MEDLINE
Journal :
Cell reports
Publication Type :
Academic Journal
Accession number :
38722743
Full Text :
https://doi.org/10.1016/j.celrep.2024.114187