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Neural signal propagation atlas of Caenorhabditis elegans

Establishing how neural function emerges from network properties is a fundamental problem in neuroscience(1). Here, to better understand the relationship between the structure and the function of a nervous system, we systematically measure signal propagation in 23,433 pairs of neurons across the hea...

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Autores principales: Randi, Francesco, Sharma, Anuj K., Dvali, Sophie, Leifer, Andrew M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632145/
https://www.ncbi.nlm.nih.gov/pubmed/37914938
http://dx.doi.org/10.1038/s41586-023-06683-4
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author Randi, Francesco
Sharma, Anuj K.
Dvali, Sophie
Leifer, Andrew M.
author_facet Randi, Francesco
Sharma, Anuj K.
Dvali, Sophie
Leifer, Andrew M.
author_sort Randi, Francesco
collection PubMed
description Establishing how neural function emerges from network properties is a fundamental problem in neuroscience(1). Here, to better understand the relationship between the structure and the function of a nervous system, we systematically measure signal propagation in 23,433 pairs of neurons across the head of the nematode Caenorhabditis elegans by direct optogenetic activation and simultaneous whole-brain calcium imaging. We measure the sign (excitatory or inhibitory), strength, temporal properties and causal direction of signal propagation between these neurons to create a functional atlas. We find that signal propagation differs from model predictions that are based on anatomy. Using mutants, we show that extrasynaptic signalling not visible from anatomy contributes to this difference. We identify many instances of dense-core-vesicle-dependent signalling, including on timescales of less than a second, that evoke acute calcium transients—often where no direct wired connection exists but where relevant neuropeptides and receptors are expressed. We propose that, in such cases, extrasynaptically released neuropeptides serve a similar function to that of classical neurotransmitters. Finally, our measured signal propagation atlas better predicts the neural dynamics of spontaneous activity than do models based on anatomy. We conclude that both synaptic and extrasynaptic signalling drive neural dynamics on short timescales, and that measurements of evoked signal propagation are crucial for interpreting neural function.
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spelling pubmed-106321452023-11-10 Neural signal propagation atlas of Caenorhabditis elegans Randi, Francesco Sharma, Anuj K. Dvali, Sophie Leifer, Andrew M. Nature Article Establishing how neural function emerges from network properties is a fundamental problem in neuroscience(1). Here, to better understand the relationship between the structure and the function of a nervous system, we systematically measure signal propagation in 23,433 pairs of neurons across the head of the nematode Caenorhabditis elegans by direct optogenetic activation and simultaneous whole-brain calcium imaging. We measure the sign (excitatory or inhibitory), strength, temporal properties and causal direction of signal propagation between these neurons to create a functional atlas. We find that signal propagation differs from model predictions that are based on anatomy. Using mutants, we show that extrasynaptic signalling not visible from anatomy contributes to this difference. We identify many instances of dense-core-vesicle-dependent signalling, including on timescales of less than a second, that evoke acute calcium transients—often where no direct wired connection exists but where relevant neuropeptides and receptors are expressed. We propose that, in such cases, extrasynaptically released neuropeptides serve a similar function to that of classical neurotransmitters. Finally, our measured signal propagation atlas better predicts the neural dynamics of spontaneous activity than do models based on anatomy. We conclude that both synaptic and extrasynaptic signalling drive neural dynamics on short timescales, and that measurements of evoked signal propagation are crucial for interpreting neural function. Nature Publishing Group UK 2023-11-01 2023 /pmc/articles/PMC10632145/ /pubmed/37914938 http://dx.doi.org/10.1038/s41586-023-06683-4 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Randi, Francesco
Sharma, Anuj K.
Dvali, Sophie
Leifer, Andrew M.
Neural signal propagation atlas of Caenorhabditis elegans
title Neural signal propagation atlas of Caenorhabditis elegans
title_full Neural signal propagation atlas of Caenorhabditis elegans
title_fullStr Neural signal propagation atlas of Caenorhabditis elegans
title_full_unstemmed Neural signal propagation atlas of Caenorhabditis elegans
title_short Neural signal propagation atlas of Caenorhabditis elegans
title_sort neural signal propagation atlas of caenorhabditis elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632145/
https://www.ncbi.nlm.nih.gov/pubmed/37914938
http://dx.doi.org/10.1038/s41586-023-06683-4
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