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Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty

The vomeronasal system (VNS) is specialized in the detection of salient chemical cues triggering social and neuroendocrine responses. Such responses are not always stereotyped, instead, they vary depending on age, sex, and reproductive state, yet the mechanisms underlying this variability are unclea...

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Autores principales: Oboti, Livio, Trova, Sara, Schellino, Roberta, Marraudino, Marilena, Harris, Natalie R., Abiona, Olubukola M., Stampar, Mojca, Lin, Weihong, Peretto, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440572/
https://www.ncbi.nlm.nih.gov/pubmed/28588456
http://dx.doi.org/10.3389/fnana.2017.00044
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author Oboti, Livio
Trova, Sara
Schellino, Roberta
Marraudino, Marilena
Harris, Natalie R.
Abiona, Olubukola M.
Stampar, Mojca
Lin, Weihong
Peretto, Paolo
author_facet Oboti, Livio
Trova, Sara
Schellino, Roberta
Marraudino, Marilena
Harris, Natalie R.
Abiona, Olubukola M.
Stampar, Mojca
Lin, Weihong
Peretto, Paolo
author_sort Oboti, Livio
collection PubMed
description The vomeronasal system (VNS) is specialized in the detection of salient chemical cues triggering social and neuroendocrine responses. Such responses are not always stereotyped, instead, they vary depending on age, sex, and reproductive state, yet the mechanisms underlying this variability are unclear. Here, by analyzing neuronal survival in the first processing nucleus of the VNS, namely the accessory olfactory bulb (AOB), through multiple bromodeoxyuridine birthdating protocols, we show that exposure of female mice to male soiled bedding material affects the integration of newborn granule interneurons mainly after puberty. This effect is induced by urine compounds produced by mature males, as bedding soiled by younger males was ineffective. The granule cell increase induced by mature male odor exposure is not prevented by pre-pubertal ovariectomy, indicating a lesser role of circulating estrogens in this plasticity. Interestingly, the intake of adult male urine-derived cues by the female vomeronasal organ increases during puberty, suggesting a direct correlation between sensory activity and AOB neuronal plasticity. Thus, as odor exposure increases the responses of newly born cells to the experienced stimuli, the addition of new GABAergic inhibitory cells to the AOB might contribute to the shaping of vomeronasal processing of male cues after puberty. Consistently, only after puberty, female mice are capable to discriminate individual male odors through the VNS.
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spelling pubmed-54405722017-06-06 Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty Oboti, Livio Trova, Sara Schellino, Roberta Marraudino, Marilena Harris, Natalie R. Abiona, Olubukola M. Stampar, Mojca Lin, Weihong Peretto, Paolo Front Neuroanat Neuroanatomy The vomeronasal system (VNS) is specialized in the detection of salient chemical cues triggering social and neuroendocrine responses. Such responses are not always stereotyped, instead, they vary depending on age, sex, and reproductive state, yet the mechanisms underlying this variability are unclear. Here, by analyzing neuronal survival in the first processing nucleus of the VNS, namely the accessory olfactory bulb (AOB), through multiple bromodeoxyuridine birthdating protocols, we show that exposure of female mice to male soiled bedding material affects the integration of newborn granule interneurons mainly after puberty. This effect is induced by urine compounds produced by mature males, as bedding soiled by younger males was ineffective. The granule cell increase induced by mature male odor exposure is not prevented by pre-pubertal ovariectomy, indicating a lesser role of circulating estrogens in this plasticity. Interestingly, the intake of adult male urine-derived cues by the female vomeronasal organ increases during puberty, suggesting a direct correlation between sensory activity and AOB neuronal plasticity. Thus, as odor exposure increases the responses of newly born cells to the experienced stimuli, the addition of new GABAergic inhibitory cells to the AOB might contribute to the shaping of vomeronasal processing of male cues after puberty. Consistently, only after puberty, female mice are capable to discriminate individual male odors through the VNS. Frontiers Media S.A. 2017-05-23 /pmc/articles/PMC5440572/ /pubmed/28588456 http://dx.doi.org/10.3389/fnana.2017.00044 Text en Copyright © 2017 Oboti, Trova, Schellino, Marraudino, Harris, Abiona, Stampar, Lin and Peretto. 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) or licensor 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 Neuroanatomy
Oboti, Livio
Trova, Sara
Schellino, Roberta
Marraudino, Marilena
Harris, Natalie R.
Abiona, Olubukola M.
Stampar, Mojca
Lin, Weihong
Peretto, Paolo
Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty
title Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty
title_full Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty
title_fullStr Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty
title_full_unstemmed Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty
title_short Activity Dependent Modulation of Granule Cell Survival in the Accessory Olfactory Bulb at Puberty
title_sort activity dependent modulation of granule cell survival in the accessory olfactory bulb at puberty
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440572/
https://www.ncbi.nlm.nih.gov/pubmed/28588456
http://dx.doi.org/10.3389/fnana.2017.00044
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