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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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 |
work_keys_str_mv |
AT rosannapsammons sizedependentaxonalboutondynamicsfollowingvisualdeprivationinvivo AT claudiaclopath sizedependentaxonalboutondynamicsfollowingvisualdeprivationinvivo AT samueljbarnes sizedependentaxonalboutondynamicsfollowingvisualdeprivationinvivo |
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1724905029497782272 |