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Adult-born neurons facilitate olfactory bulb pattern separation during task engagement

The rodent olfactory bulb incorporates thousands of newly generated inhibitory neurons daily throughout adulthood, but the role of adult neurogenesis in olfactory processing is not fully understood. Here we adopted a genetic method to inducibly suppress adult neurogenesis and investigated its effect...

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Detalles Bibliográficos
Autores principales: Li, Wankun L, Chu, Monica W, Wu, An, Suzuki, Yusuke, Imayoshi, Itaru, Komiyama, Takaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5912906/
https://www.ncbi.nlm.nih.gov/pubmed/29533179
http://dx.doi.org/10.7554/eLife.33006
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author Li, Wankun L
Chu, Monica W
Wu, An
Suzuki, Yusuke
Imayoshi, Itaru
Komiyama, Takaki
author_facet Li, Wankun L
Chu, Monica W
Wu, An
Suzuki, Yusuke
Imayoshi, Itaru
Komiyama, Takaki
author_sort Li, Wankun L
collection PubMed
description The rodent olfactory bulb incorporates thousands of newly generated inhibitory neurons daily throughout adulthood, but the role of adult neurogenesis in olfactory processing is not fully understood. Here we adopted a genetic method to inducibly suppress adult neurogenesis and investigated its effect on behavior and bulbar activity. Mice without young adult-born neurons (ABNs) showed normal ability in discriminating very different odorants but were impaired in fine discrimination. Furthermore, two-photon calcium imaging of mitral cells (MCs) revealed that the ensemble odor representations of similar odorants were more ambiguous in the ablation animals. This increased ambiguity was primarily due to a decrease in MC suppressive responses. Intriguingly, these deficits in MC encoding were only observed during task engagement but not passive exposure. Our results indicate that young olfactory ABNs are essential for the enhancement of MC pattern separation in a task engagement-dependent manner, potentially functioning as a gateway for top-down modulation.
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spelling pubmed-59129062018-04-25 Adult-born neurons facilitate olfactory bulb pattern separation during task engagement Li, Wankun L Chu, Monica W Wu, An Suzuki, Yusuke Imayoshi, Itaru Komiyama, Takaki eLife Neuroscience The rodent olfactory bulb incorporates thousands of newly generated inhibitory neurons daily throughout adulthood, but the role of adult neurogenesis in olfactory processing is not fully understood. Here we adopted a genetic method to inducibly suppress adult neurogenesis and investigated its effect on behavior and bulbar activity. Mice without young adult-born neurons (ABNs) showed normal ability in discriminating very different odorants but were impaired in fine discrimination. Furthermore, two-photon calcium imaging of mitral cells (MCs) revealed that the ensemble odor representations of similar odorants were more ambiguous in the ablation animals. This increased ambiguity was primarily due to a decrease in MC suppressive responses. Intriguingly, these deficits in MC encoding were only observed during task engagement but not passive exposure. Our results indicate that young olfactory ABNs are essential for the enhancement of MC pattern separation in a task engagement-dependent manner, potentially functioning as a gateway for top-down modulation. eLife Sciences Publications, Ltd 2018-03-13 /pmc/articles/PMC5912906/ /pubmed/29533179 http://dx.doi.org/10.7554/eLife.33006 Text en © 2018, Li et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Li, Wankun L
Chu, Monica W
Wu, An
Suzuki, Yusuke
Imayoshi, Itaru
Komiyama, Takaki
Adult-born neurons facilitate olfactory bulb pattern separation during task engagement
title Adult-born neurons facilitate olfactory bulb pattern separation during task engagement
title_full Adult-born neurons facilitate olfactory bulb pattern separation during task engagement
title_fullStr Adult-born neurons facilitate olfactory bulb pattern separation during task engagement
title_full_unstemmed Adult-born neurons facilitate olfactory bulb pattern separation during task engagement
title_short Adult-born neurons facilitate olfactory bulb pattern separation during task engagement
title_sort adult-born neurons facilitate olfactory bulb pattern separation during task engagement
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5912906/
https://www.ncbi.nlm.nih.gov/pubmed/29533179
http://dx.doi.org/10.7554/eLife.33006
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