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High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs
Layer (L) 2/3 pyramidal neurons in the primary somatosensory cortex (S1) are sparsely active, spontaneously and during sensory stimulation. Long-range inputs from higher areas may gate L2/3 activity. We investigated their in vivo impact by expressing channelrhodopsin in three main sources of feedbac...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370338/ https://www.ncbi.nlm.nih.gov/pubmed/30741160 http://dx.doi.org/10.7554/eLife.44158 |
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author | Zhang, Wanying Bruno, Randy M |
author_facet | Zhang, Wanying Bruno, Randy M |
author_sort | Zhang, Wanying |
collection | PubMed |
description | Layer (L) 2/3 pyramidal neurons in the primary somatosensory cortex (S1) are sparsely active, spontaneously and during sensory stimulation. Long-range inputs from higher areas may gate L2/3 activity. We investigated their in vivo impact by expressing channelrhodopsin in three main sources of feedback to rat S1: primary motor cortex, secondary somatosensory cortex, and secondary somatosensory thalamic nucleus (the posterior medial nucleus, POm). Inputs from cortical areas were relatively weak. POm, however, more robustly depolarized L2/3 cells and, when paired with peripheral stimulation, evoked action potentials. POm triggered not only a stronger fast-onset depolarization but also a delayed all-or-none persistent depolarization, lasting up to 1 s and exhibiting alpha/beta-range oscillations. Inactivating POm somata abolished persistent but not initial depolarization, indicating a recurrent circuit mechanism. We conclude that secondary thalamus can enhance L2/3 responsiveness over long periods. Such timescales could provide a potential modality-specific substrate for attention, working memory, and plasticity. |
format | Online Article Text |
id | pubmed-6370338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63703382019-02-15 High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs Zhang, Wanying Bruno, Randy M eLife Neuroscience Layer (L) 2/3 pyramidal neurons in the primary somatosensory cortex (S1) are sparsely active, spontaneously and during sensory stimulation. Long-range inputs from higher areas may gate L2/3 activity. We investigated their in vivo impact by expressing channelrhodopsin in three main sources of feedback to rat S1: primary motor cortex, secondary somatosensory cortex, and secondary somatosensory thalamic nucleus (the posterior medial nucleus, POm). Inputs from cortical areas were relatively weak. POm, however, more robustly depolarized L2/3 cells and, when paired with peripheral stimulation, evoked action potentials. POm triggered not only a stronger fast-onset depolarization but also a delayed all-or-none persistent depolarization, lasting up to 1 s and exhibiting alpha/beta-range oscillations. Inactivating POm somata abolished persistent but not initial depolarization, indicating a recurrent circuit mechanism. We conclude that secondary thalamus can enhance L2/3 responsiveness over long periods. Such timescales could provide a potential modality-specific substrate for attention, working memory, and plasticity. eLife Sciences Publications, Ltd 2019-02-11 /pmc/articles/PMC6370338/ /pubmed/30741160 http://dx.doi.org/10.7554/eLife.44158 Text en © 2019, Zhang and Bruno http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Zhang, Wanying Bruno, Randy M High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs |
title | High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs |
title_full | High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs |
title_fullStr | High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs |
title_full_unstemmed | High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs |
title_short | High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs |
title_sort | high-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370338/ https://www.ncbi.nlm.nih.gov/pubmed/30741160 http://dx.doi.org/10.7554/eLife.44158 |
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