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A neuromechanical model for Drosophila larval crawling based on physical measurements

BACKGROUND: Animal locomotion requires dynamic interactions between neural circuits, the body (typically muscles), and surrounding environments. While the neural circuitry of movement has been intensively studied, how these outputs are integrated with body mechanics (neuromechanics) is less clear, i...

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Autores principales: Sun, Xiyang, Liu, Yingtao, Liu, Chang, Mayumi, Koichi, Ito, Kohzo, Nose, Akinao, Kohsaka, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199175/
https://www.ncbi.nlm.nih.gov/pubmed/35701821
http://dx.doi.org/10.1186/s12915-022-01336-w
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author Sun, Xiyang
Liu, Yingtao
Liu, Chang
Mayumi, Koichi
Ito, Kohzo
Nose, Akinao
Kohsaka, Hiroshi
author_facet Sun, Xiyang
Liu, Yingtao
Liu, Chang
Mayumi, Koichi
Ito, Kohzo
Nose, Akinao
Kohsaka, Hiroshi
author_sort Sun, Xiyang
collection PubMed
description BACKGROUND: Animal locomotion requires dynamic interactions between neural circuits, the body (typically muscles), and surrounding environments. While the neural circuitry of movement has been intensively studied, how these outputs are integrated with body mechanics (neuromechanics) is less clear, in part due to the lack of understanding of the biomechanical properties of animal bodies. Here, we propose an integrated neuromechanical model of movement based on physical measurements by taking Drosophila larvae as a model of soft-bodied animals. RESULTS: We first characterized the kinematics of forward crawling in Drosophila larvae at a segmental and whole-body level. We then characterized the biomechanical parameters of fly larvae, namely the contraction forces generated by neural activity, and passive elastic and viscosity of the larval body using a stress-relaxation test. We established a mathematical neuromechanical model based on the physical measurements described above, obtaining seven kinematic values characterizing crawling locomotion. By optimizing the parameters in the neural circuit, our neuromechanical model succeeded in quantitatively reproducing the kinematics of larval locomotion that were obtained experimentally. This model could reproduce the observation of optogenetic studies reported previously. The model predicted that peristaltic locomotion could be exhibited in a low-friction condition. Analysis of floating larvae provided results consistent with this prediction. Furthermore, the model predicted a significant contribution of intersegmental connections in the central nervous system, which contrasts with a previous study. This hypothesis allowed us to make a testable prediction for the variability in intersegmental connection in sister species of the genus Drosophila. CONCLUSIONS: We generated a neurochemical model based on physical measurement to provide a new foundation to study locomotion in soft-bodied animals and soft robot engineering. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01336-w.
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spelling pubmed-91991752022-06-16 A neuromechanical model for Drosophila larval crawling based on physical measurements Sun, Xiyang Liu, Yingtao Liu, Chang Mayumi, Koichi Ito, Kohzo Nose, Akinao Kohsaka, Hiroshi BMC Biol Research Article BACKGROUND: Animal locomotion requires dynamic interactions between neural circuits, the body (typically muscles), and surrounding environments. While the neural circuitry of movement has been intensively studied, how these outputs are integrated with body mechanics (neuromechanics) is less clear, in part due to the lack of understanding of the biomechanical properties of animal bodies. Here, we propose an integrated neuromechanical model of movement based on physical measurements by taking Drosophila larvae as a model of soft-bodied animals. RESULTS: We first characterized the kinematics of forward crawling in Drosophila larvae at a segmental and whole-body level. We then characterized the biomechanical parameters of fly larvae, namely the contraction forces generated by neural activity, and passive elastic and viscosity of the larval body using a stress-relaxation test. We established a mathematical neuromechanical model based on the physical measurements described above, obtaining seven kinematic values characterizing crawling locomotion. By optimizing the parameters in the neural circuit, our neuromechanical model succeeded in quantitatively reproducing the kinematics of larval locomotion that were obtained experimentally. This model could reproduce the observation of optogenetic studies reported previously. The model predicted that peristaltic locomotion could be exhibited in a low-friction condition. Analysis of floating larvae provided results consistent with this prediction. Furthermore, the model predicted a significant contribution of intersegmental connections in the central nervous system, which contrasts with a previous study. This hypothesis allowed us to make a testable prediction for the variability in intersegmental connection in sister species of the genus Drosophila. CONCLUSIONS: We generated a neurochemical model based on physical measurement to provide a new foundation to study locomotion in soft-bodied animals and soft robot engineering. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01336-w. BioMed Central 2022-06-15 /pmc/articles/PMC9199175/ /pubmed/35701821 http://dx.doi.org/10.1186/s12915-022-01336-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Sun, Xiyang
Liu, Yingtao
Liu, Chang
Mayumi, Koichi
Ito, Kohzo
Nose, Akinao
Kohsaka, Hiroshi
A neuromechanical model for Drosophila larval crawling based on physical measurements
title A neuromechanical model for Drosophila larval crawling based on physical measurements
title_full A neuromechanical model for Drosophila larval crawling based on physical measurements
title_fullStr A neuromechanical model for Drosophila larval crawling based on physical measurements
title_full_unstemmed A neuromechanical model for Drosophila larval crawling based on physical measurements
title_short A neuromechanical model for Drosophila larval crawling based on physical measurements
title_sort neuromechanical model for drosophila larval crawling based on physical measurements
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199175/
https://www.ncbi.nlm.nih.gov/pubmed/35701821
http://dx.doi.org/10.1186/s12915-022-01336-w
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