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Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex
During cortical development, synaptic competition regulates the formation and adjustment of neuronal connectivity. It is unknown whether synaptic competition remains active in the adult brain and how inhibitory neurons participate in this process. Using morphological and electrophysiological measure...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585512/ https://www.ncbi.nlm.nih.gov/pubmed/25316336 http://dx.doi.org/10.1093/cercor/bhu245 |
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author | Saiepour, M. Hadi Chakravarthy, Sridhara Min, Rogier Levelt, Christiaan N. |
author_facet | Saiepour, M. Hadi Chakravarthy, Sridhara Min, Rogier Levelt, Christiaan N. |
author_sort | Saiepour, M. Hadi |
collection | PubMed |
description | During cortical development, synaptic competition regulates the formation and adjustment of neuronal connectivity. It is unknown whether synaptic competition remains active in the adult brain and how inhibitory neurons participate in this process. Using morphological and electrophysiological measurements, we show that expressing a dominant-negative form of the TrkB receptor (TrkB.T1) in the majority of pyramidal neurons in the adult visual cortex does not affect excitatory synapse densities. This is in stark contrast to the previously reported loss of excitatory input which occurs if the exact same transgene is expressed in sparse neurons at the same age. This indicates that synaptic competition remains active in adulthood. Additionally, we show that interneurons not expressing the TrkB.T1 transgene may have a competitive advantage and obtain more excitatory synapses when most neighboring pyramidal neurons do express the transgene. Finally, we demonstrate that inhibitory synapses onto pyramidal neurons are reduced when TrkB signaling is interfered with in most pyramidal neurons but not when few pyramidal neurons have this deficit. This adjustment of inhibitory innervation is therefore not a cell-autonomous consequence of decreased TrkB signaling but more likely a homeostatic mechanism compensating for activity changes at the population level. |
format | Online Article Text |
id | pubmed-4585512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45855122015-09-29 Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex Saiepour, M. Hadi Chakravarthy, Sridhara Min, Rogier Levelt, Christiaan N. Cereb Cortex Articles During cortical development, synaptic competition regulates the formation and adjustment of neuronal connectivity. It is unknown whether synaptic competition remains active in the adult brain and how inhibitory neurons participate in this process. Using morphological and electrophysiological measurements, we show that expressing a dominant-negative form of the TrkB receptor (TrkB.T1) in the majority of pyramidal neurons in the adult visual cortex does not affect excitatory synapse densities. This is in stark contrast to the previously reported loss of excitatory input which occurs if the exact same transgene is expressed in sparse neurons at the same age. This indicates that synaptic competition remains active in adulthood. Additionally, we show that interneurons not expressing the TrkB.T1 transgene may have a competitive advantage and obtain more excitatory synapses when most neighboring pyramidal neurons do express the transgene. Finally, we demonstrate that inhibitory synapses onto pyramidal neurons are reduced when TrkB signaling is interfered with in most pyramidal neurons but not when few pyramidal neurons have this deficit. This adjustment of inhibitory innervation is therefore not a cell-autonomous consequence of decreased TrkB signaling but more likely a homeostatic mechanism compensating for activity changes at the population level. Oxford University Press 2015-10 2014-10-14 /pmc/articles/PMC4585512/ /pubmed/25316336 http://dx.doi.org/10.1093/cercor/bhu245 Text en © The Author 2014. Published by Oxford University Press http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Articles Saiepour, M. Hadi Chakravarthy, Sridhara Min, Rogier Levelt, Christiaan N. Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex |
title | Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex |
title_full | Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex |
title_fullStr | Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex |
title_full_unstemmed | Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex |
title_short | Competition and Homeostasis of Excitatory and Inhibitory Connectivity in the Adult Mouse Visual Cortex |
title_sort | competition and homeostasis of excitatory and inhibitory connectivity in the adult mouse visual cortex |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585512/ https://www.ncbi.nlm.nih.gov/pubmed/25316336 http://dx.doi.org/10.1093/cercor/bhu245 |
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