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Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex
It has been demonstrated that sensory deprivation results in homeostatic adjustments recovering neuronal activity of the deprived cortex. For example, deprived vision multiplicatively scales up mEPSC amplitudes in the primary visual cortex, commonly referred to as synaptic scaling. However, whether...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727212/ https://www.ncbi.nlm.nih.gov/pubmed/29234064 http://dx.doi.org/10.1038/s41598-017-17711-5 |
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author | Teichert, Manuel Liebmann, Lutz Hübner, Christian A. Bolz, Jürgen |
author_facet | Teichert, Manuel Liebmann, Lutz Hübner, Christian A. Bolz, Jürgen |
author_sort | Teichert, Manuel |
collection | PubMed |
description | It has been demonstrated that sensory deprivation results in homeostatic adjustments recovering neuronal activity of the deprived cortex. For example, deprived vision multiplicatively scales up mEPSC amplitudes in the primary visual cortex, commonly referred to as synaptic scaling. However, whether synaptic scaling also occurs in auditory cortex after auditory deprivation remains elusive. Using periodic intrinsic optical imaging in adult mice, we show that conductive hearing loss (CHL), initially led to a reduction of primary auditory cortex (A1) responsiveness to sounds. However, this was followed by a complete recovery of A1 activity evoked sounds above the threshold for bone conduction, 3 days after CHL. Over the same time course patch-clamp experiments in slices revealed that mEPSC amplitudes in A1 layers 2/3 pyramids scaled up multiplicatively in CHL mice. No recovery of sensory evoked A1 activation was evident in TNFα KO animals, which lack synaptic scaling. Additionally, we could show that the suppressive effect of sounds on visually evoked visual cortex activity completely recovered along with TNFα dependent A1 homeostasis in WT animals. This is the first demonstration of homeostatic multiplicative synaptic scaling in the adult A1. These findings suggest that mild hearing loss massively affects auditory processing in adult A1. |
format | Online Article Text |
id | pubmed-5727212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57272122017-12-13 Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex Teichert, Manuel Liebmann, Lutz Hübner, Christian A. Bolz, Jürgen Sci Rep Article It has been demonstrated that sensory deprivation results in homeostatic adjustments recovering neuronal activity of the deprived cortex. For example, deprived vision multiplicatively scales up mEPSC amplitudes in the primary visual cortex, commonly referred to as synaptic scaling. However, whether synaptic scaling also occurs in auditory cortex after auditory deprivation remains elusive. Using periodic intrinsic optical imaging in adult mice, we show that conductive hearing loss (CHL), initially led to a reduction of primary auditory cortex (A1) responsiveness to sounds. However, this was followed by a complete recovery of A1 activity evoked sounds above the threshold for bone conduction, 3 days after CHL. Over the same time course patch-clamp experiments in slices revealed that mEPSC amplitudes in A1 layers 2/3 pyramids scaled up multiplicatively in CHL mice. No recovery of sensory evoked A1 activation was evident in TNFα KO animals, which lack synaptic scaling. Additionally, we could show that the suppressive effect of sounds on visually evoked visual cortex activity completely recovered along with TNFα dependent A1 homeostasis in WT animals. This is the first demonstration of homeostatic multiplicative synaptic scaling in the adult A1. These findings suggest that mild hearing loss massively affects auditory processing in adult A1. Nature Publishing Group UK 2017-12-12 /pmc/articles/PMC5727212/ /pubmed/29234064 http://dx.doi.org/10.1038/s41598-017-17711-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Teichert, Manuel Liebmann, Lutz Hübner, Christian A. Bolz, Jürgen Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex |
title | Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex |
title_full | Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex |
title_fullStr | Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex |
title_full_unstemmed | Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex |
title_short | Homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex |
title_sort | homeostatic plasticity and synaptic scaling in the adult mouse auditory cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727212/ https://www.ncbi.nlm.nih.gov/pubmed/29234064 http://dx.doi.org/10.1038/s41598-017-17711-5 |
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