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A direct interareal feedback-to-feedforward circuit in primate visual cortex

The mammalian sensory neocortex consists of hierarchically organized areas reciprocally connected via feedforward (FF) and feedback (FB) circuits. Several theories of hierarchical computation ascribe the bulk of the computational work of the cortex to looped FF-FB circuits between pairs of cortical...

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Autores principales: Siu, Caitlin, Balsor, Justin, Merlin, Sam, Federer, Frederick, Angelucci, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363744/
https://www.ncbi.nlm.nih.gov/pubmed/34389710
http://dx.doi.org/10.1038/s41467-021-24928-6
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author Siu, Caitlin
Balsor, Justin
Merlin, Sam
Federer, Frederick
Angelucci, Alessandra
author_facet Siu, Caitlin
Balsor, Justin
Merlin, Sam
Federer, Frederick
Angelucci, Alessandra
author_sort Siu, Caitlin
collection PubMed
description The mammalian sensory neocortex consists of hierarchically organized areas reciprocally connected via feedforward (FF) and feedback (FB) circuits. Several theories of hierarchical computation ascribe the bulk of the computational work of the cortex to looped FF-FB circuits between pairs of cortical areas. However, whether such corticocortical loops exist remains unclear. In higher mammals, individual FF-projection neurons send afferents almost exclusively to a single higher-level area. However, it is unclear whether FB-projection neurons show similar area-specificity, and whether they influence FF-projection neurons directly or indirectly. Using viral-mediated monosynaptic circuit tracing in macaque primary visual cortex (V1), we show that V1 neurons sending FF projections to area V2 receive monosynaptic FB inputs from V2, but not other V1-projecting areas. We also find monosynaptic FB-to-FB neuron contacts as a second motif of FB connectivity. Our results support the existence of FF-FB loops in primate cortex, and suggest that FB can rapidly and selectively influence the activity of incoming FF signals.
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spelling pubmed-83637442021-08-19 A direct interareal feedback-to-feedforward circuit in primate visual cortex Siu, Caitlin Balsor, Justin Merlin, Sam Federer, Frederick Angelucci, Alessandra Nat Commun Article The mammalian sensory neocortex consists of hierarchically organized areas reciprocally connected via feedforward (FF) and feedback (FB) circuits. Several theories of hierarchical computation ascribe the bulk of the computational work of the cortex to looped FF-FB circuits between pairs of cortical areas. However, whether such corticocortical loops exist remains unclear. In higher mammals, individual FF-projection neurons send afferents almost exclusively to a single higher-level area. However, it is unclear whether FB-projection neurons show similar area-specificity, and whether they influence FF-projection neurons directly or indirectly. Using viral-mediated monosynaptic circuit tracing in macaque primary visual cortex (V1), we show that V1 neurons sending FF projections to area V2 receive monosynaptic FB inputs from V2, but not other V1-projecting areas. We also find monosynaptic FB-to-FB neuron contacts as a second motif of FB connectivity. Our results support the existence of FF-FB loops in primate cortex, and suggest that FB can rapidly and selectively influence the activity of incoming FF signals. Nature Publishing Group UK 2021-08-13 /pmc/articles/PMC8363744/ /pubmed/34389710 http://dx.doi.org/10.1038/s41467-021-24928-6 Text en © The Author(s) 2021 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
Siu, Caitlin
Balsor, Justin
Merlin, Sam
Federer, Frederick
Angelucci, Alessandra
A direct interareal feedback-to-feedforward circuit in primate visual cortex
title A direct interareal feedback-to-feedforward circuit in primate visual cortex
title_full A direct interareal feedback-to-feedforward circuit in primate visual cortex
title_fullStr A direct interareal feedback-to-feedforward circuit in primate visual cortex
title_full_unstemmed A direct interareal feedback-to-feedforward circuit in primate visual cortex
title_short A direct interareal feedback-to-feedforward circuit in primate visual cortex
title_sort direct interareal feedback-to-feedforward circuit in primate visual cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363744/
https://www.ncbi.nlm.nih.gov/pubmed/34389710
http://dx.doi.org/10.1038/s41467-021-24928-6
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