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A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement
How does neural activity drive muscles to produce behavior? The recent development of genetic lines in Hydra that allow complete calcium imaging of both neuronal and muscle activity, as well as systematic machine learning quantification of behaviors, makes this small cnidarian an ideal model system...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089167/ https://www.ncbi.nlm.nih.gov/pubmed/36897982 http://dx.doi.org/10.1073/pnas.2210439120 |
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author | Wang, Hengji Swore, Joshua Sharma, Shashank Szymanski, John R. Yuste, Rafael Daniel, Thomas L. Regnier, Michael Bosma, Martha M. Fairhall, Adrienne L. |
author_facet | Wang, Hengji Swore, Joshua Sharma, Shashank Szymanski, John R. Yuste, Rafael Daniel, Thomas L. Regnier, Michael Bosma, Martha M. Fairhall, Adrienne L. |
author_sort | Wang, Hengji |
collection | PubMed |
description | How does neural activity drive muscles to produce behavior? The recent development of genetic lines in Hydra that allow complete calcium imaging of both neuronal and muscle activity, as well as systematic machine learning quantification of behaviors, makes this small cnidarian an ideal model system to understand and model the complete transformation from neural firing to body movements. To achieve this, we have built a neuromechanical model of Hydra’s fluid-filled hydrostatic skeleton, showing how drive by neuronal activity activates distinct patterns of muscle activity and body column biomechanics. Our model is based on experimental measurements of neuronal and muscle activity and assumes gap junctional coupling among muscle cells and calcium-dependent force generation by muscles. With these assumptions, we can robustly reproduce a basic set of Hydra’s behaviors. We can further explain puzzling experimental observations, including the dual timescale kinetics observed in muscle activation and the engagement of ectodermal and endodermal muscles in different behaviors. This work delineates the spatiotemporal control space of Hydra movement and can serve as a template for future efforts to systematically decipher the transformations in the neural basis of behavior. |
format | Online Article Text |
id | pubmed-10089167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-100891672023-09-10 A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement Wang, Hengji Swore, Joshua Sharma, Shashank Szymanski, John R. Yuste, Rafael Daniel, Thomas L. Regnier, Michael Bosma, Martha M. Fairhall, Adrienne L. Proc Natl Acad Sci U S A Biological Sciences How does neural activity drive muscles to produce behavior? The recent development of genetic lines in Hydra that allow complete calcium imaging of both neuronal and muscle activity, as well as systematic machine learning quantification of behaviors, makes this small cnidarian an ideal model system to understand and model the complete transformation from neural firing to body movements. To achieve this, we have built a neuromechanical model of Hydra’s fluid-filled hydrostatic skeleton, showing how drive by neuronal activity activates distinct patterns of muscle activity and body column biomechanics. Our model is based on experimental measurements of neuronal and muscle activity and assumes gap junctional coupling among muscle cells and calcium-dependent force generation by muscles. With these assumptions, we can robustly reproduce a basic set of Hydra’s behaviors. We can further explain puzzling experimental observations, including the dual timescale kinetics observed in muscle activation and the engagement of ectodermal and endodermal muscles in different behaviors. This work delineates the spatiotemporal control space of Hydra movement and can serve as a template for future efforts to systematically decipher the transformations in the neural basis of behavior. National Academy of Sciences 2023-03-10 2023-03-14 /pmc/articles/PMC10089167/ /pubmed/36897982 http://dx.doi.org/10.1073/pnas.2210439120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Wang, Hengji Swore, Joshua Sharma, Shashank Szymanski, John R. Yuste, Rafael Daniel, Thomas L. Regnier, Michael Bosma, Martha M. Fairhall, Adrienne L. A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement |
title | A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement |
title_full | A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement |
title_fullStr | A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement |
title_full_unstemmed | A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement |
title_short | A complete biomechanical model of Hydra contractile behaviors, from neural drive to muscle to movement |
title_sort | complete biomechanical model of hydra contractile behaviors, from neural drive to muscle to movement |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089167/ https://www.ncbi.nlm.nih.gov/pubmed/36897982 http://dx.doi.org/10.1073/pnas.2210439120 |
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