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Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans

The nervous system evaluates environmental cues and adjusts motor output to ensure navigation toward a preferred environment. The nematode Caenorhabditis elegans navigates in the thermal environment and migrates toward its cultivation temperature by moving up or down thermal gradients depending not...

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Autores principales: Ikeda, Muneki, Nakano, Shunji, Giles, Andrew C., Xu, Linghuan, Costa, Wagner Steuer, Gottschalk, Alexander, Mori, Ikue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084152/
https://www.ncbi.nlm.nih.gov/pubmed/32123108
http://dx.doi.org/10.1073/pnas.1918528117
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author Ikeda, Muneki
Nakano, Shunji
Giles, Andrew C.
Xu, Linghuan
Costa, Wagner Steuer
Gottschalk, Alexander
Mori, Ikue
author_facet Ikeda, Muneki
Nakano, Shunji
Giles, Andrew C.
Xu, Linghuan
Costa, Wagner Steuer
Gottschalk, Alexander
Mori, Ikue
author_sort Ikeda, Muneki
collection PubMed
description The nervous system evaluates environmental cues and adjusts motor output to ensure navigation toward a preferred environment. The nematode Caenorhabditis elegans navigates in the thermal environment and migrates toward its cultivation temperature by moving up or down thermal gradients depending not only on absolute temperature but on relative difference between current and previously experienced cultivation temperature. Although previous studies showed that such thermal context-dependent opposing migration is mediated by bias in frequency and direction of reorientation behavior, the complete neural pathways—from sensory to motor neurons—and their circuit logics underlying the opposing behavioral bias remain elusive. By conducting comprehensive cell ablation, high-resolution behavioral analyses, and computational modeling, we identified multiple neural pathways regulating behavioral components important for thermotaxis, and demonstrate that distinct sets of neurons are required for opposing bias of even single behavioral components. Furthermore, our imaging analyses show that the context-dependent operation is evident in sensory neurons, very early in the neural pathway, and manifested by bidirectional responses of a first-layer interneuron AIB under different thermal contexts. Our results suggest that the contextual differences are encoded among sensory neurons and a first-layer interneuron, processed among different downstream neurons, and lead to the flexible execution of context-dependent behavior.
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spelling pubmed-70841522020-03-24 Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans Ikeda, Muneki Nakano, Shunji Giles, Andrew C. Xu, Linghuan Costa, Wagner Steuer Gottschalk, Alexander Mori, Ikue Proc Natl Acad Sci U S A Biological Sciences The nervous system evaluates environmental cues and adjusts motor output to ensure navigation toward a preferred environment. The nematode Caenorhabditis elegans navigates in the thermal environment and migrates toward its cultivation temperature by moving up or down thermal gradients depending not only on absolute temperature but on relative difference between current and previously experienced cultivation temperature. Although previous studies showed that such thermal context-dependent opposing migration is mediated by bias in frequency and direction of reorientation behavior, the complete neural pathways—from sensory to motor neurons—and their circuit logics underlying the opposing behavioral bias remain elusive. By conducting comprehensive cell ablation, high-resolution behavioral analyses, and computational modeling, we identified multiple neural pathways regulating behavioral components important for thermotaxis, and demonstrate that distinct sets of neurons are required for opposing bias of even single behavioral components. Furthermore, our imaging analyses show that the context-dependent operation is evident in sensory neurons, very early in the neural pathway, and manifested by bidirectional responses of a first-layer interneuron AIB under different thermal contexts. Our results suggest that the contextual differences are encoded among sensory neurons and a first-layer interneuron, processed among different downstream neurons, and lead to the flexible execution of context-dependent behavior. National Academy of Sciences 2020-03-17 2020-03-02 /pmc/articles/PMC7084152/ /pubmed/32123108 http://dx.doi.org/10.1073/pnas.1918528117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Ikeda, Muneki
Nakano, Shunji
Giles, Andrew C.
Xu, Linghuan
Costa, Wagner Steuer
Gottschalk, Alexander
Mori, Ikue
Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans
title Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans
title_full Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans
title_fullStr Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans
title_full_unstemmed Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans
title_short Context-dependent operation of neural circuits underlies a navigation behavior in Caenorhabditis elegans
title_sort context-dependent operation of neural circuits underlies a navigation behavior in caenorhabditis elegans
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084152/
https://www.ncbi.nlm.nih.gov/pubmed/32123108
http://dx.doi.org/10.1073/pnas.1918528117
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