Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In Vivo

Persistent synapses are thought to underpin the storage of sensory experience, yet little is known about their structural plasticity in vivo. We investigated how persistent presynaptic structures respond to the loss of primary sensory input. Using in vivo two-photon (2P) imaging, we measured fluctua...

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Main Authors: Rosanna P. Sammons, Claudia Clopath, Samuel J. Barnes
Format: Article
Language:English
Published: Elsevier 2018-01-01
Series:Cell Reports
Subjects:
LTP
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124717319022
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spelling doaj-bab4710f799a4876874d2d406d35123a2020-11-25T02:13:28ZengElsevierCell Reports2211-12472018-01-0122357658410.1016/j.celrep.2017.12.065Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In VivoRosanna P. Sammons0Claudia Clopath1Samuel J. Barnes2Department of Neuroscience, Physiology and Pharmacology, University College London, 21 University St., London WC1E 6DE, UKDepartment of Biomedical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, UKDivision of Brain Sciences, Department of Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London W12 0NN, UKPersistent synapses are thought to underpin the storage of sensory experience, yet little is known about their structural plasticity in vivo. We investigated how persistent presynaptic structures respond to the loss of primary sensory input. Using in vivo two-photon (2P) imaging, we measured fluctuations in the size of excitatory axonal boutons in L2/3 of adult mouse visual cortex after monocular enucleation. The average size of boutons did not change after deprivation, but the range of bouton sizes was reduced. Large boutons decreased, and small boutons increased. Reduced bouton variance was accompanied by a reduced range of correlated calcium-mediated neural activity in L2/3 of awake animals. Network simulations predicted that size-dependent plasticity may promote conditions of greater bidirectional plasticity. These predictions were supported by electrophysiological measures of short- and long-term plasticity. We propose size-dependent dynamics facilitate cortical reorganization by maximizing the potential for bidirectional plasticity.http://www.sciencedirect.com/science/article/pii/S2211124717319022visual cortexaxonal boutonpopulation couplingpresynapticplasticityGCaMPnetworkhomeostasissensory deprivationLTP
collection DOAJ
language English
format Article
sources DOAJ
author Rosanna P. Sammons
Claudia Clopath
Samuel J. Barnes
spellingShingle Rosanna P. Sammons
Claudia Clopath
Samuel J. Barnes
Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In Vivo
Cell Reports
visual cortex
axonal bouton
population coupling
presynaptic
plasticity
GCaMP
network
homeostasis
sensory deprivation
LTP
author_facet Rosanna P. Sammons
Claudia Clopath
Samuel J. Barnes
author_sort Rosanna P. Sammons
title Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In Vivo
title_short Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In Vivo
title_full Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In Vivo
title_fullStr Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In Vivo
title_full_unstemmed Size-Dependent Axonal Bouton Dynamics following Visual Deprivation In Vivo
title_sort size-dependent axonal bouton dynamics following visual deprivation in vivo
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2018-01-01
description Persistent synapses are thought to underpin the storage of sensory experience, yet little is known about their structural plasticity in vivo. We investigated how persistent presynaptic structures respond to the loss of primary sensory input. Using in vivo two-photon (2P) imaging, we measured fluctuations in the size of excitatory axonal boutons in L2/3 of adult mouse visual cortex after monocular enucleation. The average size of boutons did not change after deprivation, but the range of bouton sizes was reduced. Large boutons decreased, and small boutons increased. Reduced bouton variance was accompanied by a reduced range of correlated calcium-mediated neural activity in L2/3 of awake animals. Network simulations predicted that size-dependent plasticity may promote conditions of greater bidirectional plasticity. These predictions were supported by electrophysiological measures of short- and long-term plasticity. We propose size-dependent dynamics facilitate cortical reorganization by maximizing the potential for bidirectional plasticity.
topic visual cortex
axonal bouton
population coupling
presynaptic
plasticity
GCaMP
network
homeostasis
sensory deprivation
LTP
url http://www.sciencedirect.com/science/article/pii/S2211124717319022
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