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Distinct organization of two cortico-cortical feedback pathways
Neocortical feedback is critical for attention, prediction, and learning. To mechanically understand its function requires deciphering its cell-type wiring. Recent studies revealed that feedback between primary motor to primary somatosensory areas in mice is disinhibitory, targeting vasoactive intes...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613627/ https://www.ncbi.nlm.nih.gov/pubmed/36302912 http://dx.doi.org/10.1038/s41467-022-33883-9 |
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author | Shen, Shan Jiang, Xiaolong Scala, Federico Fu, Jiakun Fahey, Paul Kobak, Dmitry Tan, Zhenghuan Zhou, Na Reimer, Jacob Sinz, Fabian Tolias, Andreas S. |
author_facet | Shen, Shan Jiang, Xiaolong Scala, Federico Fu, Jiakun Fahey, Paul Kobak, Dmitry Tan, Zhenghuan Zhou, Na Reimer, Jacob Sinz, Fabian Tolias, Andreas S. |
author_sort | Shen, Shan |
collection | PubMed |
description | Neocortical feedback is critical for attention, prediction, and learning. To mechanically understand its function requires deciphering its cell-type wiring. Recent studies revealed that feedback between primary motor to primary somatosensory areas in mice is disinhibitory, targeting vasoactive intestinal peptide-expressing interneurons, in addition to pyramidal cells. It is unknown whether this circuit motif represents a general cortico-cortical feedback organizing principle. Here we show that in contrast to this wiring rule, feedback between higher-order lateromedial visual area to primary visual cortex preferentially activates somatostatin-expressing interneurons. Functionally, both feedback circuits temporally sharpen feed-forward excitation eliciting a transient increase–followed by a prolonged decrease–in pyramidal cell activity under sustained feed-forward input. However, under feed-forward transient input, the primary motor to primary somatosensory cortex feedback facilitates bursting while lateromedial area to primary visual cortex feedback increases time precision. Our findings argue for multiple cortico-cortical feedback motifs implementing different dynamic non-linear operations. |
format | Online Article Text |
id | pubmed-9613627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96136272022-10-29 Distinct organization of two cortico-cortical feedback pathways Shen, Shan Jiang, Xiaolong Scala, Federico Fu, Jiakun Fahey, Paul Kobak, Dmitry Tan, Zhenghuan Zhou, Na Reimer, Jacob Sinz, Fabian Tolias, Andreas S. Nat Commun Article Neocortical feedback is critical for attention, prediction, and learning. To mechanically understand its function requires deciphering its cell-type wiring. Recent studies revealed that feedback between primary motor to primary somatosensory areas in mice is disinhibitory, targeting vasoactive intestinal peptide-expressing interneurons, in addition to pyramidal cells. It is unknown whether this circuit motif represents a general cortico-cortical feedback organizing principle. Here we show that in contrast to this wiring rule, feedback between higher-order lateromedial visual area to primary visual cortex preferentially activates somatostatin-expressing interneurons. Functionally, both feedback circuits temporally sharpen feed-forward excitation eliciting a transient increase–followed by a prolonged decrease–in pyramidal cell activity under sustained feed-forward input. However, under feed-forward transient input, the primary motor to primary somatosensory cortex feedback facilitates bursting while lateromedial area to primary visual cortex feedback increases time precision. Our findings argue for multiple cortico-cortical feedback motifs implementing different dynamic non-linear operations. Nature Publishing Group UK 2022-10-27 /pmc/articles/PMC9613627/ /pubmed/36302912 http://dx.doi.org/10.1038/s41467-022-33883-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Shen, Shan Jiang, Xiaolong Scala, Federico Fu, Jiakun Fahey, Paul Kobak, Dmitry Tan, Zhenghuan Zhou, Na Reimer, Jacob Sinz, Fabian Tolias, Andreas S. Distinct organization of two cortico-cortical feedback pathways |
title | Distinct organization of two cortico-cortical feedback pathways |
title_full | Distinct organization of two cortico-cortical feedback pathways |
title_fullStr | Distinct organization of two cortico-cortical feedback pathways |
title_full_unstemmed | Distinct organization of two cortico-cortical feedback pathways |
title_short | Distinct organization of two cortico-cortical feedback pathways |
title_sort | distinct organization of two cortico-cortical feedback pathways |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613627/ https://www.ncbi.nlm.nih.gov/pubmed/36302912 http://dx.doi.org/10.1038/s41467-022-33883-9 |
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