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Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation

Recently, a new type of Caenorhabditis elegans associative learning was reported, where nematodes learn to reach a target arm in an empty T‐maze, after they have successfully located reward (food) in the same side arm of a similar, baited, training maze. Here, we present a simplified mathematical mo...

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Autores principales: Sakelaris, Bennet G., Li, Zongyu, Sun, Jiawei, Banerjee, Shurjo, Booth, Victoria, Gourgou, Eleni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269982/
https://www.ncbi.nlm.nih.gov/pubmed/34894022
http://dx.doi.org/10.1111/ejn.15560
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author Sakelaris, Bennet G.
Li, Zongyu
Sun, Jiawei
Banerjee, Shurjo
Booth, Victoria
Gourgou, Eleni
author_facet Sakelaris, Bennet G.
Li, Zongyu
Sun, Jiawei
Banerjee, Shurjo
Booth, Victoria
Gourgou, Eleni
author_sort Sakelaris, Bennet G.
collection PubMed
description Recently, a new type of Caenorhabditis elegans associative learning was reported, where nematodes learn to reach a target arm in an empty T‐maze, after they have successfully located reward (food) in the same side arm of a similar, baited, training maze. Here, we present a simplified mathematical model of C. elegans chemosensory and locomotive circuitry that replicates C. elegans navigation in a T‐maze and predicts the underlying mechanisms generating maze learning. Based on known neural circuitry, the model circuit responds to food‐released chemical cues by modulating motor neuron activity that drives simulated locomotion. We show that, through modulation of interneuron activity, such a circuit can mediate maze learning by acquiring a turning bias, even after a single training session. Simulated nematode maze navigation during training conditions in food‐baited mazes and during testing conditions in empty mazes is validated by comparing simulated behaviour with new experimental video data, extracted through the implementation of a custom‐made maze tracking algorithm. Our work provides a mathematical framework for investigating the neural mechanisms underlying this novel learning behaviour in C. elegans . Model results predict neuronal components involved in maze and spatial learning and identify target neurons and potential neural mechanisms for future experimental investigations into this learning behaviour.
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spelling pubmed-92699822022-07-22 Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation Sakelaris, Bennet G. Li, Zongyu Sun, Jiawei Banerjee, Shurjo Booth, Victoria Gourgou, Eleni Eur J Neurosci Behavioral Neuroscience Recently, a new type of Caenorhabditis elegans associative learning was reported, where nematodes learn to reach a target arm in an empty T‐maze, after they have successfully located reward (food) in the same side arm of a similar, baited, training maze. Here, we present a simplified mathematical model of C. elegans chemosensory and locomotive circuitry that replicates C. elegans navigation in a T‐maze and predicts the underlying mechanisms generating maze learning. Based on known neural circuitry, the model circuit responds to food‐released chemical cues by modulating motor neuron activity that drives simulated locomotion. We show that, through modulation of interneuron activity, such a circuit can mediate maze learning by acquiring a turning bias, even after a single training session. Simulated nematode maze navigation during training conditions in food‐baited mazes and during testing conditions in empty mazes is validated by comparing simulated behaviour with new experimental video data, extracted through the implementation of a custom‐made maze tracking algorithm. Our work provides a mathematical framework for investigating the neural mechanisms underlying this novel learning behaviour in C. elegans . Model results predict neuronal components involved in maze and spatial learning and identify target neurons and potential neural mechanisms for future experimental investigations into this learning behaviour. John Wiley and Sons Inc. 2022-01-09 2022-01 /pmc/articles/PMC9269982/ /pubmed/34894022 http://dx.doi.org/10.1111/ejn.15560 Text en © 2021 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Behavioral Neuroscience
Sakelaris, Bennet G.
Li, Zongyu
Sun, Jiawei
Banerjee, Shurjo
Booth, Victoria
Gourgou, Eleni
Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation
title Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation
title_full Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation
title_fullStr Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation
title_full_unstemmed Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation
title_short Modelling learning in Caenorhabditis elegans chemosensory and locomotive circuitry for T‐maze navigation
title_sort modelling learning in caenorhabditis elegans chemosensory and locomotive circuitry for t‐maze navigation
topic Behavioral Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269982/
https://www.ncbi.nlm.nih.gov/pubmed/34894022
http://dx.doi.org/10.1111/ejn.15560
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