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Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans
Neural circuits coordinate with muscles and sensory feedback to generate motor behaviors appropriate to an animal’s environment. In C. elegans, the mechanisms by which the motor circuit generates undulations and modulates them based on the environment are largely unclear. We quantitatively analyzed...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560089/ https://www.ncbi.nlm.nih.gov/pubmed/34569934 http://dx.doi.org/10.7554/eLife.69905 |
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author | Ji, Hongfei Fouad, Anthony D Teng, Shelly Liu, Alice Alvarez-Illera, Pilar Yao, Bowen Li, Zihao Fang-Yen, Christopher |
author_facet | Ji, Hongfei Fouad, Anthony D Teng, Shelly Liu, Alice Alvarez-Illera, Pilar Yao, Bowen Li, Zihao Fang-Yen, Christopher |
author_sort | Ji, Hongfei |
collection | PubMed |
description | Neural circuits coordinate with muscles and sensory feedback to generate motor behaviors appropriate to an animal’s environment. In C. elegans, the mechanisms by which the motor circuit generates undulations and modulates them based on the environment are largely unclear. We quantitatively analyzed C. elegans locomotion during free movement and during transient optogenetic muscle inhibition. Undulatory movements were highly asymmetrical with respect to the duration of bending and unbending during each cycle. Phase response curves induced by brief optogenetic inhibition of head muscles showed gradual increases and rapid decreases as a function of phase at which the perturbation was applied. A relaxation oscillator model based on proprioceptive thresholds that switch the active muscle moment was developed and is shown to quantitatively agree with data from free movement, phase responses, and previous results for gait adaptation to mechanical loadings. Our results suggest a neuromuscular mechanism underlying C. elegans motor pattern generation within a compact circuit. |
format | Online Article Text |
id | pubmed-8560089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-85600892021-11-03 Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans Ji, Hongfei Fouad, Anthony D Teng, Shelly Liu, Alice Alvarez-Illera, Pilar Yao, Bowen Li, Zihao Fang-Yen, Christopher eLife Computational and Systems Biology Neural circuits coordinate with muscles and sensory feedback to generate motor behaviors appropriate to an animal’s environment. In C. elegans, the mechanisms by which the motor circuit generates undulations and modulates them based on the environment are largely unclear. We quantitatively analyzed C. elegans locomotion during free movement and during transient optogenetic muscle inhibition. Undulatory movements were highly asymmetrical with respect to the duration of bending and unbending during each cycle. Phase response curves induced by brief optogenetic inhibition of head muscles showed gradual increases and rapid decreases as a function of phase at which the perturbation was applied. A relaxation oscillator model based on proprioceptive thresholds that switch the active muscle moment was developed and is shown to quantitatively agree with data from free movement, phase responses, and previous results for gait adaptation to mechanical loadings. Our results suggest a neuromuscular mechanism underlying C. elegans motor pattern generation within a compact circuit. eLife Sciences Publications, Ltd 2021-09-27 /pmc/articles/PMC8560089/ /pubmed/34569934 http://dx.doi.org/10.7554/eLife.69905 Text en © 2021, Ji et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Ji, Hongfei Fouad, Anthony D Teng, Shelly Liu, Alice Alvarez-Illera, Pilar Yao, Bowen Li, Zihao Fang-Yen, Christopher Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans |
title | Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans |
title_full | Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans |
title_fullStr | Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans |
title_full_unstemmed | Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans |
title_short | Phase response analyses support a relaxation oscillator model of locomotor rhythm generation in Caenorhabditis elegans |
title_sort | phase response analyses support a relaxation oscillator model of locomotor rhythm generation in caenorhabditis elegans |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560089/ https://www.ncbi.nlm.nih.gov/pubmed/34569934 http://dx.doi.org/10.7554/eLife.69905 |
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