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Locomotion modulates olfactory learning through proprioception in C. elegans

Locomotor activities can enhance learning, but the underlying circuit and synaptic mechanisms are largely unknown. Here we show that locomotion facilitates aversive olfactory learning in C. elegans by activating mechanoreceptors in motor neurons, and transmitting the proprioceptive information thus...

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Autores principales: Zhan, Xu, Chen, Chao, Niu, Longgang, Du, Xinran, Lei, Ying, Dan, Rui, Wang, Zhao-Wen, Liu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374624/
https://www.ncbi.nlm.nih.gov/pubmed/37500635
http://dx.doi.org/10.1038/s41467-023-40286-x
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author Zhan, Xu
Chen, Chao
Niu, Longgang
Du, Xinran
Lei, Ying
Dan, Rui
Wang, Zhao-Wen
Liu, Ping
author_facet Zhan, Xu
Chen, Chao
Niu, Longgang
Du, Xinran
Lei, Ying
Dan, Rui
Wang, Zhao-Wen
Liu, Ping
author_sort Zhan, Xu
collection PubMed
description Locomotor activities can enhance learning, but the underlying circuit and synaptic mechanisms are largely unknown. Here we show that locomotion facilitates aversive olfactory learning in C. elegans by activating mechanoreceptors in motor neurons, and transmitting the proprioceptive information thus generated to locomotion interneurons through antidromic-rectifying gap junctions. The proprioceptive information serves to regulate experience-dependent activities and functional coupling of interneurons that process olfactory sensory information to produce the learning behavior. Genetic destruction of either the mechanoreceptors in motor neurons, the rectifying gap junctions between the motor neurons and locomotion interneurons, or specific inhibitory synapses among the interneurons impairs the aversive olfactory learning. We have thus uncovered an unexpected role of proprioception in a specific learning behavior as well as the circuit, synaptic, and gene bases for this function.
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spelling pubmed-103746242023-07-29 Locomotion modulates olfactory learning through proprioception in C. elegans Zhan, Xu Chen, Chao Niu, Longgang Du, Xinran Lei, Ying Dan, Rui Wang, Zhao-Wen Liu, Ping Nat Commun Article Locomotor activities can enhance learning, but the underlying circuit and synaptic mechanisms are largely unknown. Here we show that locomotion facilitates aversive olfactory learning in C. elegans by activating mechanoreceptors in motor neurons, and transmitting the proprioceptive information thus generated to locomotion interneurons through antidromic-rectifying gap junctions. The proprioceptive information serves to regulate experience-dependent activities and functional coupling of interneurons that process olfactory sensory information to produce the learning behavior. Genetic destruction of either the mechanoreceptors in motor neurons, the rectifying gap junctions between the motor neurons and locomotion interneurons, or specific inhibitory synapses among the interneurons impairs the aversive olfactory learning. We have thus uncovered an unexpected role of proprioception in a specific learning behavior as well as the circuit, synaptic, and gene bases for this function. Nature Publishing Group UK 2023-07-27 /pmc/articles/PMC10374624/ /pubmed/37500635 http://dx.doi.org/10.1038/s41467-023-40286-x 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
Zhan, Xu
Chen, Chao
Niu, Longgang
Du, Xinran
Lei, Ying
Dan, Rui
Wang, Zhao-Wen
Liu, Ping
Locomotion modulates olfactory learning through proprioception in C. elegans
title Locomotion modulates olfactory learning through proprioception in C. elegans
title_full Locomotion modulates olfactory learning through proprioception in C. elegans
title_fullStr Locomotion modulates olfactory learning through proprioception in C. elegans
title_full_unstemmed Locomotion modulates olfactory learning through proprioception in C. elegans
title_short Locomotion modulates olfactory learning through proprioception in C. elegans
title_sort locomotion modulates olfactory learning through proprioception in c. elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374624/
https://www.ncbi.nlm.nih.gov/pubmed/37500635
http://dx.doi.org/10.1038/s41467-023-40286-x
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