Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Shen, Shan, Jiang, Xiaolong, Scala, Federico, Fu, Jiakun, Fahey, Paul, Kobak, Dmitry, Tan, Zhenghuan, Zhou, Na, Reimer, Jacob, Sinz, Fabian, Tolias, Andreas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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
_version_ 1784820017668292608
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
work_keys_str_mv AT shenshan distinctorganizationoftwocorticocorticalfeedbackpathways
AT jiangxiaolong distinctorganizationoftwocorticocorticalfeedbackpathways
AT scalafederico distinctorganizationoftwocorticocorticalfeedbackpathways
AT fujiakun distinctorganizationoftwocorticocorticalfeedbackpathways
AT faheypaul distinctorganizationoftwocorticocorticalfeedbackpathways
AT kobakdmitry distinctorganizationoftwocorticocorticalfeedbackpathways
AT tanzhenghuan distinctorganizationoftwocorticocorticalfeedbackpathways
AT zhouna distinctorganizationoftwocorticocorticalfeedbackpathways
AT reimerjacob distinctorganizationoftwocorticocorticalfeedbackpathways
AT sinzfabian distinctorganizationoftwocorticocorticalfeedbackpathways
AT toliasandreass distinctorganizationoftwocorticocorticalfeedbackpathways