Cargando…

Feedforward and feedback interactions between visual cortical areas use different population activity patterns

Brain function relies on the coordination of activity across multiple, recurrently connected brain areas. For instance, sensory information encoded in early sensory areas is relayed to, and further processed by, higher cortical areas and then fed back. However, the way in which feedforward and feedb...

Descripción completa

Detalles Bibliográficos
Autores principales: Semedo, João D., Jasper, Anna I., Zandvakili, Amin, Krishna, Aravind, Aschner, Amir, Machens, Christian K., Kohn, Adam, Yu, Byron M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888615/
https://www.ncbi.nlm.nih.gov/pubmed/35232956
http://dx.doi.org/10.1038/s41467-022-28552-w
_version_ 1784661198325678080
author Semedo, João D.
Jasper, Anna I.
Zandvakili, Amin
Krishna, Aravind
Aschner, Amir
Machens, Christian K.
Kohn, Adam
Yu, Byron M.
author_facet Semedo, João D.
Jasper, Anna I.
Zandvakili, Amin
Krishna, Aravind
Aschner, Amir
Machens, Christian K.
Kohn, Adam
Yu, Byron M.
author_sort Semedo, João D.
collection PubMed
description Brain function relies on the coordination of activity across multiple, recurrently connected brain areas. For instance, sensory information encoded in early sensory areas is relayed to, and further processed by, higher cortical areas and then fed back. However, the way in which feedforward and feedback signaling interact with one another is incompletely understood. Here we investigate this question by leveraging simultaneous neuronal population recordings in early and midlevel visual areas (V1–V2 and V1–V4). Using a dimensionality reduction approach, we find that population interactions are feedforward-dominated shortly after stimulus onset and feedback-dominated during spontaneous activity. The population activity patterns most correlated across areas were distinct during feedforward- and feedback-dominated periods. These results suggest that feedforward and feedback signaling rely on separate “channels”, which allows feedback signals to not directly affect activity that is fed forward.
format Online
Article
Text
id pubmed-8888615
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-88886152022-03-17 Feedforward and feedback interactions between visual cortical areas use different population activity patterns Semedo, João D. Jasper, Anna I. Zandvakili, Amin Krishna, Aravind Aschner, Amir Machens, Christian K. Kohn, Adam Yu, Byron M. Nat Commun Article Brain function relies on the coordination of activity across multiple, recurrently connected brain areas. For instance, sensory information encoded in early sensory areas is relayed to, and further processed by, higher cortical areas and then fed back. However, the way in which feedforward and feedback signaling interact with one another is incompletely understood. Here we investigate this question by leveraging simultaneous neuronal population recordings in early and midlevel visual areas (V1–V2 and V1–V4). Using a dimensionality reduction approach, we find that population interactions are feedforward-dominated shortly after stimulus onset and feedback-dominated during spontaneous activity. The population activity patterns most correlated across areas were distinct during feedforward- and feedback-dominated periods. These results suggest that feedforward and feedback signaling rely on separate “channels”, which allows feedback signals to not directly affect activity that is fed forward. Nature Publishing Group UK 2022-03-01 /pmc/articles/PMC8888615/ /pubmed/35232956 http://dx.doi.org/10.1038/s41467-022-28552-w 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
Semedo, João D.
Jasper, Anna I.
Zandvakili, Amin
Krishna, Aravind
Aschner, Amir
Machens, Christian K.
Kohn, Adam
Yu, Byron M.
Feedforward and feedback interactions between visual cortical areas use different population activity patterns
title Feedforward and feedback interactions between visual cortical areas use different population activity patterns
title_full Feedforward and feedback interactions between visual cortical areas use different population activity patterns
title_fullStr Feedforward and feedback interactions between visual cortical areas use different population activity patterns
title_full_unstemmed Feedforward and feedback interactions between visual cortical areas use different population activity patterns
title_short Feedforward and feedback interactions between visual cortical areas use different population activity patterns
title_sort feedforward and feedback interactions between visual cortical areas use different population activity patterns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888615/
https://www.ncbi.nlm.nih.gov/pubmed/35232956
http://dx.doi.org/10.1038/s41467-022-28552-w
work_keys_str_mv AT semedojoaod feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns
AT jasperannai feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns
AT zandvakiliamin feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns
AT krishnaaravind feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns
AT aschneramir feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns
AT machenschristiank feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns
AT kohnadam feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns
AT yubyronm feedforwardandfeedbackinteractionsbetweenvisualcorticalareasusedifferentpopulationactivitypatterns