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Rapid and continuous activity-dependent plasticity of olfactory sensory input

Incorporation of new neurons enables plasticity and repair of circuits in the adult brain. Adult neurogenesis is a key feature of the mammalian olfactory system, with new olfactory sensory neurons (OSNs) wiring into highly organized olfactory bulb (OB) circuits throughout life. However, neither when...

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Detalles Bibliográficos
Autores principales: Cheetham, Claire E. J., Park, Una, Belluscio, Leonardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764868/
https://www.ncbi.nlm.nih.gov/pubmed/26898529
http://dx.doi.org/10.1038/ncomms10729
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author Cheetham, Claire E. J.
Park, Una
Belluscio, Leonardo
author_facet Cheetham, Claire E. J.
Park, Una
Belluscio, Leonardo
author_sort Cheetham, Claire E. J.
collection PubMed
description Incorporation of new neurons enables plasticity and repair of circuits in the adult brain. Adult neurogenesis is a key feature of the mammalian olfactory system, with new olfactory sensory neurons (OSNs) wiring into highly organized olfactory bulb (OB) circuits throughout life. However, neither when new postnatally generated OSNs first form synapses nor whether OSNs retain the capacity for synaptogenesis once mature, is known. Therefore, how integration of adult-born OSNs may contribute to lifelong OB plasticity is unclear. Here, we use a combination of electron microscopy, optogenetic activation and in vivo time-lapse imaging to show that newly generated OSNs form highly dynamic synapses and are capable of eliciting robust stimulus-locked firing of neurons in the mouse OB. Furthermore, we demonstrate that mature OSN axons undergo continuous activity-dependent synaptic remodelling that persists into adulthood. OSN synaptogenesis, therefore, provides a sustained potential for OB plasticity and repair that is much faster than OSN replacement alone.
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spelling pubmed-47648682016-03-04 Rapid and continuous activity-dependent plasticity of olfactory sensory input Cheetham, Claire E. J. Park, Una Belluscio, Leonardo Nat Commun Article Incorporation of new neurons enables plasticity and repair of circuits in the adult brain. Adult neurogenesis is a key feature of the mammalian olfactory system, with new olfactory sensory neurons (OSNs) wiring into highly organized olfactory bulb (OB) circuits throughout life. However, neither when new postnatally generated OSNs first form synapses nor whether OSNs retain the capacity for synaptogenesis once mature, is known. Therefore, how integration of adult-born OSNs may contribute to lifelong OB plasticity is unclear. Here, we use a combination of electron microscopy, optogenetic activation and in vivo time-lapse imaging to show that newly generated OSNs form highly dynamic synapses and are capable of eliciting robust stimulus-locked firing of neurons in the mouse OB. Furthermore, we demonstrate that mature OSN axons undergo continuous activity-dependent synaptic remodelling that persists into adulthood. OSN synaptogenesis, therefore, provides a sustained potential for OB plasticity and repair that is much faster than OSN replacement alone. Nature Publishing Group 2016-02-22 /pmc/articles/PMC4764868/ /pubmed/26898529 http://dx.doi.org/10.1038/ncomms10729 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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
Cheetham, Claire E. J.
Park, Una
Belluscio, Leonardo
Rapid and continuous activity-dependent plasticity of olfactory sensory input
title Rapid and continuous activity-dependent plasticity of olfactory sensory input
title_full Rapid and continuous activity-dependent plasticity of olfactory sensory input
title_fullStr Rapid and continuous activity-dependent plasticity of olfactory sensory input
title_full_unstemmed Rapid and continuous activity-dependent plasticity of olfactory sensory input
title_short Rapid and continuous activity-dependent plasticity of olfactory sensory input
title_sort rapid and continuous activity-dependent plasticity of olfactory sensory input
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764868/
https://www.ncbi.nlm.nih.gov/pubmed/26898529
http://dx.doi.org/10.1038/ncomms10729
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