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

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 a...

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Autores principales: Trouillet, Anne-Charlotte, Moussu, Chantal, Poissenot, Kevin, Keller, Matthieu, Birnbaumer, Lutz, Leinders-Zufall, Trese, Zufall, Frank, Chamero, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925392/
https://www.ncbi.nlm.nih.gov/pubmed/33679330
http://dx.doi.org/10.3389/fncel.2021.638800
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author Trouillet, Anne-Charlotte
Moussu, Chantal
Poissenot, Kevin
Keller, Matthieu
Birnbaumer, Lutz
Leinders-Zufall, Trese
Zufall, Frank
Chamero, Pablo
author_facet Trouillet, Anne-Charlotte
Moussu, Chantal
Poissenot, Kevin
Keller, Matthieu
Birnbaumer, Lutz
Leinders-Zufall, Trese
Zufall, Frank
Chamero, Pablo
author_sort Trouillet, Anne-Charlotte
collection PubMed
description 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.
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spelling pubmed-79253922021-03-04 Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice Trouillet, Anne-Charlotte Moussu, Chantal Poissenot, Kevin Keller, Matthieu Birnbaumer, Lutz Leinders-Zufall, Trese Zufall, Frank Chamero, Pablo Front Cell Neurosci Cellular Neuroscience 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. Frontiers Media S.A. 2021-02-17 /pmc/articles/PMC7925392/ /pubmed/33679330 http://dx.doi.org/10.3389/fncel.2021.638800 Text en Copyright © 2021 Trouillet, Moussu, Poissenot, Keller, Birnbaumer, Leinders-Zufall, Zufall and Chamero. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Trouillet, Anne-Charlotte
Moussu, Chantal
Poissenot, Kevin
Keller, Matthieu
Birnbaumer, Lutz
Leinders-Zufall, Trese
Zufall, Frank
Chamero, Pablo
Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice
title Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice
title_full Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice
title_fullStr Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice
title_full_unstemmed Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice
title_short Sensory Detection by the Vomeronasal Organ Modulates Experience-Dependent Social Behaviors in Female Mice
title_sort sensory detection by the vomeronasal organ modulates experience-dependent social behaviors in female mice
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925392/
https://www.ncbi.nlm.nih.gov/pubmed/33679330
http://dx.doi.org/10.3389/fncel.2021.638800
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