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Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex
Recent studies have shown that ocular dominance plasticity in layer 2/3 of the visual cortex exhibits a form of homeostatic plasticity that is related to synaptic scaling and depends on TNFα. In this study, we tested whether a similar form of plasticity was present in layer 2/3 of the barrel cortex...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247584/ https://www.ncbi.nlm.nih.gov/pubmed/28093546 http://dx.doi.org/10.1098/rstb.2016.0150 |
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author | Glazewski, Stanislaw Greenhill, Stuart Fox, Kevin |
author_facet | Glazewski, Stanislaw Greenhill, Stuart Fox, Kevin |
author_sort | Glazewski, Stanislaw |
collection | PubMed |
description | Recent studies have shown that ocular dominance plasticity in layer 2/3 of the visual cortex exhibits a form of homeostatic plasticity that is related to synaptic scaling and depends on TNFα. In this study, we tested whether a similar form of plasticity was present in layer 2/3 of the barrel cortex and, therefore, whether the mechanism was likely to be a general property of cortical neurons. We found that whisker deprivation could induce homeostatic plasticity in layer 2/3 of barrel cortex, but not in a mouse strain lacking synaptic scaling. The time-course of homeostatic plasticity in layer 2/3 was similar to that of L5 regular spiking (RS) neurons (L5RS), but slower than that of L5 intrinsic bursting (IB) neurons (L5IB). In layer 5, the strength of evoked whisker responses and ex vivo miniature excitatory post-synaptic currents (mEPSCs) amplitudes showed an identical time-course for homeostatic plasticity, implying that plasticity at excitatory synapses contacting layer 5 neurons is sufficient to explain the changes in evoked responses. Spontaneous firing rate also showed homeostatic behaviour for L5IB cells, but was absent for L5RS cells over the time-course studied. Spontaneous firing rate homeostasis was found to be independent of evoked response homeostasis suggesting that the two depend on different mechanisms. This article is part of the themed issue ‘Integrating Hebbian and homeostatic plasticity’. |
format | Online Article Text |
id | pubmed-5247584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-52475842017-03-05 Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex Glazewski, Stanislaw Greenhill, Stuart Fox, Kevin Philos Trans R Soc Lond B Biol Sci Articles Recent studies have shown that ocular dominance plasticity in layer 2/3 of the visual cortex exhibits a form of homeostatic plasticity that is related to synaptic scaling and depends on TNFα. In this study, we tested whether a similar form of plasticity was present in layer 2/3 of the barrel cortex and, therefore, whether the mechanism was likely to be a general property of cortical neurons. We found that whisker deprivation could induce homeostatic plasticity in layer 2/3 of barrel cortex, but not in a mouse strain lacking synaptic scaling. The time-course of homeostatic plasticity in layer 2/3 was similar to that of L5 regular spiking (RS) neurons (L5RS), but slower than that of L5 intrinsic bursting (IB) neurons (L5IB). In layer 5, the strength of evoked whisker responses and ex vivo miniature excitatory post-synaptic currents (mEPSCs) amplitudes showed an identical time-course for homeostatic plasticity, implying that plasticity at excitatory synapses contacting layer 5 neurons is sufficient to explain the changes in evoked responses. Spontaneous firing rate also showed homeostatic behaviour for L5IB cells, but was absent for L5RS cells over the time-course studied. Spontaneous firing rate homeostasis was found to be independent of evoked response homeostasis suggesting that the two depend on different mechanisms. This article is part of the themed issue ‘Integrating Hebbian and homeostatic plasticity’. The Royal Society 2017-03-05 /pmc/articles/PMC5247584/ /pubmed/28093546 http://dx.doi.org/10.1098/rstb.2016.0150 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Glazewski, Stanislaw Greenhill, Stuart Fox, Kevin Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex |
title | Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex |
title_full | Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex |
title_fullStr | Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex |
title_full_unstemmed | Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex |
title_short | Time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex |
title_sort | time-course and mechanisms of homeostatic plasticity in layers 2/3 and 5 of the barrel cortex |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247584/ https://www.ncbi.nlm.nih.gov/pubmed/28093546 http://dx.doi.org/10.1098/rstb.2016.0150 |
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