Cargando…

Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity

There is convincing evidence that the deprivation of one sense can lead to adaptive neuronal changes in spared primary sensory cortices. However, the repercussions of late-onset sensory deprivations on functionality of the remaining sensory cortices are poorly understood. Using repeated intrinsic si...

Descripción completa

Detalles Bibliográficos
Autores principales: Teichert, Manuel, Isstas, Marcel, Liebmann, Lutz, Hübner, Christian A., Wieske, Franziska, Winter, Christine, Lehmann, Konrad, Bolz, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411125/
https://www.ncbi.nlm.nih.gov/pubmed/30856226
http://dx.doi.org/10.1371/journal.pone.0213616
_version_ 1783402343919779840
author Teichert, Manuel
Isstas, Marcel
Liebmann, Lutz
Hübner, Christian A.
Wieske, Franziska
Winter, Christine
Lehmann, Konrad
Bolz, Jürgen
author_facet Teichert, Manuel
Isstas, Marcel
Liebmann, Lutz
Hübner, Christian A.
Wieske, Franziska
Winter, Christine
Lehmann, Konrad
Bolz, Jürgen
author_sort Teichert, Manuel
collection PubMed
description There is convincing evidence that the deprivation of one sense can lead to adaptive neuronal changes in spared primary sensory cortices. However, the repercussions of late-onset sensory deprivations on functionality of the remaining sensory cortices are poorly understood. Using repeated intrinsic signal imaging we investigated the effects of whisker or auditory deprivation (WD or AD, respectively) on responsiveness of the binocular primary visual cortex (V1) in fully adult mice. The binocular zone of mice is innervated by both eyes, with the contralateral eye always dominating V1 input over ipsilateral eye input, the normal ocular dominance (OD) ratio. Strikingly, we found that 3 days of WD or AD induced a transient shift of OD, which was mediated by a potentiation of V1 input through the ipsilateral eye. This cross-modal effect was accompanied by strengthening of layer 4 synapses in V1, required visual experience through the ipsilateral eye and was mediated by an increase of the excitation/inhibition ratio in V1. Finally, we demonstrate that both WD and AD induced a long-lasting improvement of visual performance. Our data provide evidence that the deprivation of a non-visual sensory modality cross-modally induces experience dependent V1 plasticity and improves visual behavior, even in adult mice.
format Online
Article
Text
id pubmed-6411125
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-64111252019-04-01 Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity Teichert, Manuel Isstas, Marcel Liebmann, Lutz Hübner, Christian A. Wieske, Franziska Winter, Christine Lehmann, Konrad Bolz, Jürgen PLoS One Research Article There is convincing evidence that the deprivation of one sense can lead to adaptive neuronal changes in spared primary sensory cortices. However, the repercussions of late-onset sensory deprivations on functionality of the remaining sensory cortices are poorly understood. Using repeated intrinsic signal imaging we investigated the effects of whisker or auditory deprivation (WD or AD, respectively) on responsiveness of the binocular primary visual cortex (V1) in fully adult mice. The binocular zone of mice is innervated by both eyes, with the contralateral eye always dominating V1 input over ipsilateral eye input, the normal ocular dominance (OD) ratio. Strikingly, we found that 3 days of WD or AD induced a transient shift of OD, which was mediated by a potentiation of V1 input through the ipsilateral eye. This cross-modal effect was accompanied by strengthening of layer 4 synapses in V1, required visual experience through the ipsilateral eye and was mediated by an increase of the excitation/inhibition ratio in V1. Finally, we demonstrate that both WD and AD induced a long-lasting improvement of visual performance. Our data provide evidence that the deprivation of a non-visual sensory modality cross-modally induces experience dependent V1 plasticity and improves visual behavior, even in adult mice. Public Library of Science 2019-03-11 /pmc/articles/PMC6411125/ /pubmed/30856226 http://dx.doi.org/10.1371/journal.pone.0213616 Text en © 2019 Teichert et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Teichert, Manuel
Isstas, Marcel
Liebmann, Lutz
Hübner, Christian A.
Wieske, Franziska
Winter, Christine
Lehmann, Konrad
Bolz, Jürgen
Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity
title Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity
title_full Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity
title_fullStr Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity
title_full_unstemmed Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity
title_short Visual deprivation independent shift of ocular dominance induced by cross-modal plasticity
title_sort visual deprivation independent shift of ocular dominance induced by cross-modal plasticity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411125/
https://www.ncbi.nlm.nih.gov/pubmed/30856226
http://dx.doi.org/10.1371/journal.pone.0213616
work_keys_str_mv AT teichertmanuel visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity
AT isstasmarcel visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity
AT liebmannlutz visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity
AT hubnerchristiana visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity
AT wieskefranziska visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity
AT winterchristine visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity
AT lehmannkonrad visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity
AT bolzjurgen visualdeprivationindependentshiftofoculardominanceinducedbycrossmodalplasticity