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Gait Modulation in C. elegans: An Integrated Neuromechanical Model

Equipped with its 302-cell nervous system, the nematode Caenorhabditis elegans adapts its locomotion in different environments, exhibiting so-called swimming in liquids and crawling on dense gels. Recent experiments have demonstrated that the worm displays the full range of intermediate behaviors wh...

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Detalles Bibliográficos
Autores principales: Boyle, Jordan H., Berri, Stefano, Cohen, Netta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296079/
https://www.ncbi.nlm.nih.gov/pubmed/22408616
http://dx.doi.org/10.3389/fncom.2012.00010
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author Boyle, Jordan H.
Berri, Stefano
Cohen, Netta
author_facet Boyle, Jordan H.
Berri, Stefano
Cohen, Netta
author_sort Boyle, Jordan H.
collection PubMed
description Equipped with its 302-cell nervous system, the nematode Caenorhabditis elegans adapts its locomotion in different environments, exhibiting so-called swimming in liquids and crawling on dense gels. Recent experiments have demonstrated that the worm displays the full range of intermediate behaviors when placed in intermediate environments. The continuous nature of this transition strongly suggests that these behaviors all stem from modulation of a single underlying mechanism. We present a model of C. elegans forward locomotion that includes a neuromuscular control system that relies on a sensory feedback mechanism to generate undulations and is integrated with a physical model of the body and environment. We find that the model reproduces the entire swim-crawl transition, as well as locomotion in complex and heterogeneous environments. This is achieved with no modulatory mechanism, except via the proprioceptive response to the physical environment. Manipulations of the model are used to dissect the proposed pattern generation mechanism and its modulation. The model suggests a possible role for GABAergic D-class neurons in forward locomotion and makes a number of experimental predictions, in particular with respect to non-linearities in the model and to symmetry breaking between the neuromuscular systems on the ventral and dorsal sides of the body.
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spelling pubmed-32960792012-03-09 Gait Modulation in C. elegans: An Integrated Neuromechanical Model Boyle, Jordan H. Berri, Stefano Cohen, Netta Front Comput Neurosci Neuroscience Equipped with its 302-cell nervous system, the nematode Caenorhabditis elegans adapts its locomotion in different environments, exhibiting so-called swimming in liquids and crawling on dense gels. Recent experiments have demonstrated that the worm displays the full range of intermediate behaviors when placed in intermediate environments. The continuous nature of this transition strongly suggests that these behaviors all stem from modulation of a single underlying mechanism. We present a model of C. elegans forward locomotion that includes a neuromuscular control system that relies on a sensory feedback mechanism to generate undulations and is integrated with a physical model of the body and environment. We find that the model reproduces the entire swim-crawl transition, as well as locomotion in complex and heterogeneous environments. This is achieved with no modulatory mechanism, except via the proprioceptive response to the physical environment. Manipulations of the model are used to dissect the proposed pattern generation mechanism and its modulation. The model suggests a possible role for GABAergic D-class neurons in forward locomotion and makes a number of experimental predictions, in particular with respect to non-linearities in the model and to symmetry breaking between the neuromuscular systems on the ventral and dorsal sides of the body. Frontiers Research Foundation 2012-03-07 /pmc/articles/PMC3296079/ /pubmed/22408616 http://dx.doi.org/10.3389/fncom.2012.00010 Text en Copyright © 2012 Boyle, Berri and Cohen. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroscience
Boyle, Jordan H.
Berri, Stefano
Cohen, Netta
Gait Modulation in C. elegans: An Integrated Neuromechanical Model
title Gait Modulation in C. elegans: An Integrated Neuromechanical Model
title_full Gait Modulation in C. elegans: An Integrated Neuromechanical Model
title_fullStr Gait Modulation in C. elegans: An Integrated Neuromechanical Model
title_full_unstemmed Gait Modulation in C. elegans: An Integrated Neuromechanical Model
title_short Gait Modulation in C. elegans: An Integrated Neuromechanical Model
title_sort gait modulation in c. elegans: an integrated neuromechanical model
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296079/
https://www.ncbi.nlm.nih.gov/pubmed/22408616
http://dx.doi.org/10.3389/fncom.2012.00010
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