Cerebellar dopamine D2 receptors regulate social behaviors.


Journal

Nature neuroscience
ISSN: 1546-1726
Titre abrégé: Nat Neurosci
Pays: United States
ID NLM: 9809671

Informations de publication

Date de publication:
07 2022
Historique:
received: 08 01 2020
accepted: 10 05 2022
pubmed: 18 6 2022
medline: 15 7 2022
entrez: 17 6 2022
Statut: ppublish

Résumé

The cerebellum, a primary brain structure involved in the control of sensorimotor tasks, also contributes to higher cognitive functions including reward, emotion and social interaction. Although the regulation of these behaviors has been largely ascribed to the monoaminergic system in limbic regions, the contribution of cerebellar dopamine signaling in the modulation of these functions remains largely unknown. By combining cell-type-specific transcriptomics, histological analyses, three-dimensional imaging and patch-clamp recordings, we demonstrate that cerebellar dopamine D2 receptors (D2Rs) in mice are preferentially expressed in Purkinje cells (PCs) and regulate synaptic efficacy onto PCs. Moreover, we found that changes in D2R levels in PCs of male mice during adulthood alter sociability and preference for social novelty without affecting motor functions. Altogether, these findings demonstrate novel roles for D2R in PC function and causally link cerebellar D2R levels of expression to social behaviors.

Identifiants

pubmed: 35710984
doi: 10.1038/s41593-022-01092-8
pii: 10.1038/s41593-022-01092-8
doi:

Substances chimiques

Receptors, Dopamine D1 0
Receptors, Dopamine D2 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

900-911

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc.

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Auteurs

Laura Cutando (L)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France. laura.cutando@uab.cat.
Institut de Neurociències and Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Bellaterra, Spain. laura.cutando@uab.cat.

Emma Puighermanal (E)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France.
Institut de Neurociències, Universitat Autònoma de Barcelona, Bellaterra, Spain.

Laia Castell (L)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France.

Pauline Tarot (P)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France.

Morgane Belle (M)

Institut de la Vision, Sorbonne Université, INSERM, CNRS, Paris, France.

Federica Bertaso (F)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France.

Margarita Arango-Lievano (M)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France.

Fabrice Ango (F)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France.
INM, Univ. Montpellier, CNRS, Inserm, Montpellier, France.

Marcelo Rubinstein (M)

Instituto de Investigaciones en Ingeniería Genética y Biología Molecular, CONICET; FCEN, Universidad de Buenos Aires, Buenos Aires, Argentina; and Department of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI, USA.

Albert Quintana (A)

Institut de Neurociències and Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Bellaterra, Spain.

Alain Chédotal (A)

Institut de la Vision, Sorbonne Université, INSERM, CNRS, Paris, France.

Manuel Mameli (M)

Department of Fundamental Neuroscience, University of Lausanne, Lausanne, Switzerland.
Inserm UMR-S 1270, Paris, France.

Emmanuel Valjent (E)

IGF, Univ. Montpellier, CNRS, Inserm, Montpellier, France. emmanuel.valjent@igf.cnrs.fr.

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