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Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities
Thalamic inputs of cells in sensory cortices are outnumbered by local connections. Thus, it was suggested that robust sensory response in layer 4 emerges due to synchronized thalamic activity. To investigate the role of both inputs in the generation of correlated cortical activities, we isolated the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027246/ https://www.ncbi.nlm.nih.gov/pubmed/27615520 http://dx.doi.org/10.1038/ncomms12740 |
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author | Cohen-Kashi Malina, Katayun Mohar, Boaz Rappaport, Akiva N. Lampl, Ilan |
author_facet | Cohen-Kashi Malina, Katayun Mohar, Boaz Rappaport, Akiva N. Lampl, Ilan |
author_sort | Cohen-Kashi Malina, Katayun |
collection | PubMed |
description | Thalamic inputs of cells in sensory cortices are outnumbered by local connections. Thus, it was suggested that robust sensory response in layer 4 emerges due to synchronized thalamic activity. To investigate the role of both inputs in the generation of correlated cortical activities, we isolated the thalamic excitatory inputs of cortical cells by optogenetically silencing cortical firing. In anaesthetized mice, we measured the correlation between isolated thalamic synaptic inputs of simultaneously patched nearby layer 4 cells of the barrel cortex. Here we report that in contrast to correlated activity of excitatory synaptic inputs in the intact cortex, isolated thalamic inputs exhibit lower variability and asynchronous spontaneous and sensory-evoked inputs. These results are further supported in awake mice when we recorded the excitatory inputs of individual cortical cells simultaneously with the local field potential in a nearby site. Our results therefore indicate that cortical synchronization emerges by intracortical coupling. |
format | Online Article Text |
id | pubmed-5027246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50272462016-09-23 Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities Cohen-Kashi Malina, Katayun Mohar, Boaz Rappaport, Akiva N. Lampl, Ilan Nat Commun Article Thalamic inputs of cells in sensory cortices are outnumbered by local connections. Thus, it was suggested that robust sensory response in layer 4 emerges due to synchronized thalamic activity. To investigate the role of both inputs in the generation of correlated cortical activities, we isolated the thalamic excitatory inputs of cortical cells by optogenetically silencing cortical firing. In anaesthetized mice, we measured the correlation between isolated thalamic synaptic inputs of simultaneously patched nearby layer 4 cells of the barrel cortex. Here we report that in contrast to correlated activity of excitatory synaptic inputs in the intact cortex, isolated thalamic inputs exhibit lower variability and asynchronous spontaneous and sensory-evoked inputs. These results are further supported in awake mice when we recorded the excitatory inputs of individual cortical cells simultaneously with the local field potential in a nearby site. Our results therefore indicate that cortical synchronization emerges by intracortical coupling. Nature Publishing Group 2016-09-12 /pmc/articles/PMC5027246/ /pubmed/27615520 http://dx.doi.org/10.1038/ncomms12740 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Cohen-Kashi Malina, Katayun Mohar, Boaz Rappaport, Akiva N. Lampl, Ilan Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities |
title | Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities |
title_full | Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities |
title_fullStr | Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities |
title_full_unstemmed | Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities |
title_short | Local and thalamic origins of correlated ongoing and sensory-evoked cortical activities |
title_sort | local and thalamic origins of correlated ongoing and sensory-evoked cortical activities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027246/ https://www.ncbi.nlm.nih.gov/pubmed/27615520 http://dx.doi.org/10.1038/ncomms12740 |
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