Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice.

Gαi2 kisspeptin lordosis maternal olfactory sex preference

Journal

Frontiers in cellular neuroscience
ISSN: 1662-5102
Titre abrégé: Front Cell Neurosci
Pays: Switzerland
ID NLM: 101477935

Informations de publication

Date de publication:
2021
Historique:
received: 07 12 2020
accepted: 28 01 2021
entrez: 8 3 2021
pubmed: 9 3 2021
medline: 9 3 2021
Statut: epublish

Résumé

In mice, social behaviors are largely controlled by the olfactory system. Pheromone detection induces naïve virgin females to retrieve isolated pups to the nest and to be sexually receptive to males, but social experience increases the performance of both types of innate behaviors. Whether animals are intrinsically sensitive to the smell of conspecifics, or the detection of olfactory cues modulates experience for the display of social responses is currently unclear. Here, we employed mice with an olfactory-specific deletion of the G protein Gαi2, which partially eliminates sensory function in the vomeronasal organ (VNO), to show that social behavior in female mice results from interactions between intrinsic mechanisms in the vomeronasal system and experience-dependent plasticity. In pup- and sexually-naïve females, Gαi2 deletion elicited a reduction in pup retrieval behavior, but not in sexual receptivity. By contrast, experienced animals showed normal maternal behavior, but the experience-dependent increase in sexual receptivity was incomplete. Further, lower receptivity was accompanied by reduced neuronal activity in the anterior accessory olfactory bulb and the rostral periventricular area of the third ventricle. Therefore, neural mechanisms utilize intrinsic sensitivity in the mouse vomeronasal system and enable plasticity to display consistent social behavior.

Identifiants

pubmed: 33679330
doi: 10.3389/fncel.2021.638800
pmc: PMC7925392
doi:

Types de publication

Journal Article

Langues

eng

Pagination

638800

Subventions

Organisme : Intramural NIH HHS
ID : Z01 ES101643
Pays : United States

Informations de copyright

Copyright © 2021 Trouillet, Moussu, Poissenot, Keller, Birnbaumer, Leinders-Zufall, Zufall and Chamero.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Anne-Charlotte Trouillet (AC)

Laboratoire de Physiologie de la Reproduction et des Comportements, UMR 0085 INRAE-CNRS-IFCE-University of Tours, Nouzilly, France.

Chantal Moussu (C)

Laboratoire de Physiologie de la Reproduction et des Comportements, UMR 0085 INRAE-CNRS-IFCE-University of Tours, Nouzilly, France.

Kevin Poissenot (K)

Laboratoire de Physiologie de la Reproduction et des Comportements, UMR 0085 INRAE-CNRS-IFCE-University of Tours, Nouzilly, France.

Matthieu Keller (M)

Laboratoire de Physiologie de la Reproduction et des Comportements, UMR 0085 INRAE-CNRS-IFCE-University of Tours, Nouzilly, France.

Lutz Birnbaumer (L)

Neurobiology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Durham, NC, United States.
School of Medical Sciences, Institute of Biomedical Research (BIOMED), Catholic University of Argentina, Buenos Aires, Argentina.

Trese Leinders-Zufall (T)

Center for Integrative Physiology and Molecular Medicine, Saarland University, Homburg, Germany.

Frank Zufall (F)

Center for Integrative Physiology and Molecular Medicine, Saarland University, Homburg, Germany.

Pablo Chamero (P)

Laboratoire de Physiologie de la Reproduction et des Comportements, UMR 0085 INRAE-CNRS-IFCE-University of Tours, Nouzilly, France.

Classifications MeSH