Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Hengji, Swore, Joshua, Sharma, Shashank, Szymanski, John R., Yuste, Rafael, Daniel, Thomas L., Regnier, Michael, Bosma, Martha M., Fairhall, Adrienne L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
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
_version_ 1785022713004294144
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
work_keys_str_mv AT wanghengji acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT sworejoshua acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT sharmashashank acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT szymanskijohnr acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT yusterafael acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT danielthomasl acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT regniermichael acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT bosmamartham acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT fairhalladriennel acompletebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT wanghengji completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT sworejoshua completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT sharmashashank completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT szymanskijohnr completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT yusterafael completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT danielthomasl completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT regniermichael completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT bosmamartham completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement
AT fairhalladriennel completebiomechanicalmodelofhydracontractilebehaviorsfromneuraldrivetomuscletomovement