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Inferring neural signalling directionality from undirected structural connectomes

Neural information flow is inherently directional. To date, investigation of directional communication in the human structural connectome has been precluded by the inability of non-invasive neuroimaging methods to resolve axonal directionality. Here, we demonstrate that decentralized measures of net...

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Detalles Bibliográficos
Autores principales: Seguin, Caio, Razi, Adeel, Zalesky, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753104/
https://www.ncbi.nlm.nih.gov/pubmed/31537787
http://dx.doi.org/10.1038/s41467-019-12201-w
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author Seguin, Caio
Razi, Adeel
Zalesky, Andrew
author_facet Seguin, Caio
Razi, Adeel
Zalesky, Andrew
author_sort Seguin, Caio
collection PubMed
description Neural information flow is inherently directional. To date, investigation of directional communication in the human structural connectome has been precluded by the inability of non-invasive neuroimaging methods to resolve axonal directionality. Here, we demonstrate that decentralized measures of network communication, applied to the undirected topology and geometry of brain networks, can infer putative directions of large-scale neural signalling. We propose the concept of send-receive communication asymmetry to characterize cortical regions as senders, receivers or neutral, based on differences between their incoming and outgoing communication efficiencies. Our results reveal a send-receive cortical hierarchy that recapitulates established organizational gradients differentiating sensory-motor and multimodal areas. We find that send-receive asymmetries are significantly associated with the directionality of effective connectivity derived from spectral dynamic causal modeling. Finally, using fruit fly, mouse and macaque connectomes, we provide further evidence suggesting that directionality of neural signalling is significantly encoded in the undirected architecture of nervous systems.
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spelling pubmed-67531042019-09-23 Inferring neural signalling directionality from undirected structural connectomes Seguin, Caio Razi, Adeel Zalesky, Andrew Nat Commun Article Neural information flow is inherently directional. To date, investigation of directional communication in the human structural connectome has been precluded by the inability of non-invasive neuroimaging methods to resolve axonal directionality. Here, we demonstrate that decentralized measures of network communication, applied to the undirected topology and geometry of brain networks, can infer putative directions of large-scale neural signalling. We propose the concept of send-receive communication asymmetry to characterize cortical regions as senders, receivers or neutral, based on differences between their incoming and outgoing communication efficiencies. Our results reveal a send-receive cortical hierarchy that recapitulates established organizational gradients differentiating sensory-motor and multimodal areas. We find that send-receive asymmetries are significantly associated with the directionality of effective connectivity derived from spectral dynamic causal modeling. Finally, using fruit fly, mouse and macaque connectomes, we provide further evidence suggesting that directionality of neural signalling is significantly encoded in the undirected architecture of nervous systems. Nature Publishing Group UK 2019-09-19 /pmc/articles/PMC6753104/ /pubmed/31537787 http://dx.doi.org/10.1038/s41467-019-12201-w Text en © The Author(s) 2019 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/.
spellingShingle Article
Seguin, Caio
Razi, Adeel
Zalesky, Andrew
Inferring neural signalling directionality from undirected structural connectomes
title Inferring neural signalling directionality from undirected structural connectomes
title_full Inferring neural signalling directionality from undirected structural connectomes
title_fullStr Inferring neural signalling directionality from undirected structural connectomes
title_full_unstemmed Inferring neural signalling directionality from undirected structural connectomes
title_short Inferring neural signalling directionality from undirected structural connectomes
title_sort inferring neural signalling directionality from undirected structural connectomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753104/
https://www.ncbi.nlm.nih.gov/pubmed/31537787
http://dx.doi.org/10.1038/s41467-019-12201-w
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