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Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb
Adult-born neurons adjust olfactory bulb (OB) network functioning in response to changing environmental conditions by the formation, retraction and/or stabilization of new synaptic contacts. While some changes in the odour environment are rapid, the synaptogenesis of adult-born neurons occurs over a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013674/ https://www.ncbi.nlm.nih.gov/pubmed/27578235 http://dx.doi.org/10.1038/ncomms12659 |
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author | Breton-Provencher, Vincent Bakhshetyan, Karen Hardy, Delphine Bammann, Rodrigo Roberto Cavarretta, Francesco Snapyan, Marina Côté, Daniel Migliore, Michele Saghatelyan, Armen |
author_facet | Breton-Provencher, Vincent Bakhshetyan, Karen Hardy, Delphine Bammann, Rodrigo Roberto Cavarretta, Francesco Snapyan, Marina Côté, Daniel Migliore, Michele Saghatelyan, Armen |
author_sort | Breton-Provencher, Vincent |
collection | PubMed |
description | Adult-born neurons adjust olfactory bulb (OB) network functioning in response to changing environmental conditions by the formation, retraction and/or stabilization of new synaptic contacts. While some changes in the odour environment are rapid, the synaptogenesis of adult-born neurons occurs over a longer time scale. It remains unknown how the bulbar network functions when rapid and persistent changes in environmental conditions occur but when new synapses have not been formed. Here we reveal a new form of structural remodelling where mature spines of adult-born but not early-born neurons relocate in an activity-dependent manner. Principal cell activity induces directional growth of spine head filopodia (SHF) followed by spine relocation. Principal cell-derived glutamate and BDNF regulate SHF motility and directional spine relocation, respectively; and spines with SHF are selectively preserved following sensory deprivation. Our three-dimensional model suggests that spine relocation allows fast reorganization of OB network with functional consequences for odour information processing. |
format | Online Article Text |
id | pubmed-5013674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50136742016-09-20 Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb Breton-Provencher, Vincent Bakhshetyan, Karen Hardy, Delphine Bammann, Rodrigo Roberto Cavarretta, Francesco Snapyan, Marina Côté, Daniel Migliore, Michele Saghatelyan, Armen Nat Commun Article Adult-born neurons adjust olfactory bulb (OB) network functioning in response to changing environmental conditions by the formation, retraction and/or stabilization of new synaptic contacts. While some changes in the odour environment are rapid, the synaptogenesis of adult-born neurons occurs over a longer time scale. It remains unknown how the bulbar network functions when rapid and persistent changes in environmental conditions occur but when new synapses have not been formed. Here we reveal a new form of structural remodelling where mature spines of adult-born but not early-born neurons relocate in an activity-dependent manner. Principal cell activity induces directional growth of spine head filopodia (SHF) followed by spine relocation. Principal cell-derived glutamate and BDNF regulate SHF motility and directional spine relocation, respectively; and spines with SHF are selectively preserved following sensory deprivation. Our three-dimensional model suggests that spine relocation allows fast reorganization of OB network with functional consequences for odour information processing. Nature Publishing Group 2016-08-31 /pmc/articles/PMC5013674/ /pubmed/27578235 http://dx.doi.org/10.1038/ncomms12659 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Breton-Provencher, Vincent Bakhshetyan, Karen Hardy, Delphine Bammann, Rodrigo Roberto Cavarretta, Francesco Snapyan, Marina Côté, Daniel Migliore, Michele Saghatelyan, Armen Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb |
title | Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb |
title_full | Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb |
title_fullStr | Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb |
title_full_unstemmed | Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb |
title_short | Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb |
title_sort | principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013674/ https://www.ncbi.nlm.nih.gov/pubmed/27578235 http://dx.doi.org/10.1038/ncomms12659 |
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