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The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior

The adult mouse olfactory bulb is continuously supplied with new neurons that mostly differentiate into granule cells (GCs). Different subtypes of adult-born GCs have been identified, but their maturational profiles and their roles in bulbar network functioning and odor behavior remain elusive. It i...

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Autores principales: Hardy, Delphine, Malvaut, Sarah, Breton-Provencher, Vincent, Saghatelyan, Armen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010413/
https://www.ncbi.nlm.nih.gov/pubmed/29925844
http://dx.doi.org/10.1038/s41598-018-27692-8
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author Hardy, Delphine
Malvaut, Sarah
Breton-Provencher, Vincent
Saghatelyan, Armen
author_facet Hardy, Delphine
Malvaut, Sarah
Breton-Provencher, Vincent
Saghatelyan, Armen
author_sort Hardy, Delphine
collection PubMed
description The adult mouse olfactory bulb is continuously supplied with new neurons that mostly differentiate into granule cells (GCs). Different subtypes of adult-born GCs have been identified, but their maturational profiles and their roles in bulbar network functioning and odor behavior remain elusive. It is also not known whether the same subpopulations of GCs born during early postnatal life (early-born) or during adulthood (adult-born) differ in their morpho-functional properties. Here, we show that adult-born calretinin-expressing (CR(+)) and non-expressing (CR(−)) GCs, as well as early-born CR(+) GCs, display distinct inhibitory inputs but indistinguishable excitatory inputs and similar morphological characteristics. The frequencies of inhibitory post-synaptic currents were lower in early-born and adult-born CR(+) GCs than in adult-born CR(−) neurons. These findings were corroborated by the reduced density of gephyrin(+) puncta on CR(+) GCs. CR(+) GCs displayed a higher level of activation following olfactory tasks based on odor discrimination, as determined by an immediate early gene expression analysis. Pharmacogenetic inhibition of CR(+) GCs diminished the ability of the mice to discriminate complex odor mixtures. Altogether, our results indicate that distinct inhibitory inputs are received by adult-born CR(+) and CR(−) GCs, that early- and adult-born CR(+) neurons have similar morpho-functional properties, and that CR(+) GCs are involved in complex odor discrimination tasks.
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spelling pubmed-60104132018-07-06 The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior Hardy, Delphine Malvaut, Sarah Breton-Provencher, Vincent Saghatelyan, Armen Sci Rep Article The adult mouse olfactory bulb is continuously supplied with new neurons that mostly differentiate into granule cells (GCs). Different subtypes of adult-born GCs have been identified, but their maturational profiles and their roles in bulbar network functioning and odor behavior remain elusive. It is also not known whether the same subpopulations of GCs born during early postnatal life (early-born) or during adulthood (adult-born) differ in their morpho-functional properties. Here, we show that adult-born calretinin-expressing (CR(+)) and non-expressing (CR(−)) GCs, as well as early-born CR(+) GCs, display distinct inhibitory inputs but indistinguishable excitatory inputs and similar morphological characteristics. The frequencies of inhibitory post-synaptic currents were lower in early-born and adult-born CR(+) GCs than in adult-born CR(−) neurons. These findings were corroborated by the reduced density of gephyrin(+) puncta on CR(+) GCs. CR(+) GCs displayed a higher level of activation following olfactory tasks based on odor discrimination, as determined by an immediate early gene expression analysis. Pharmacogenetic inhibition of CR(+) GCs diminished the ability of the mice to discriminate complex odor mixtures. Altogether, our results indicate that distinct inhibitory inputs are received by adult-born CR(+) and CR(−) GCs, that early- and adult-born CR(+) neurons have similar morpho-functional properties, and that CR(+) GCs are involved in complex odor discrimination tasks. Nature Publishing Group UK 2018-06-20 /pmc/articles/PMC6010413/ /pubmed/29925844 http://dx.doi.org/10.1038/s41598-018-27692-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hardy, Delphine
Malvaut, Sarah
Breton-Provencher, Vincent
Saghatelyan, Armen
The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
title The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
title_full The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
title_fullStr The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
title_full_unstemmed The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
title_short The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
title_sort role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010413/
https://www.ncbi.nlm.nih.gov/pubmed/29925844
http://dx.doi.org/10.1038/s41598-018-27692-8
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