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An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity
A repetitive gait cycle is an archetypical component within the behavioral repertoire of many animals including humans. It originates from mechanical feedback within proprioceptors to adjust the motor program during locomotion and thus leads to a periodic orbit in a low-dimensional space. Here, we i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448456/ https://www.ncbi.nlm.nih.gov/pubmed/34533987 http://dx.doi.org/10.1126/sciadv.abg4617 |
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author | Das, Ravi Lin, Li-Chun Català-Castro, Frederic Malaiwong, Nawaphat Sanfeliu-Cerdán, Neus Porta-de-la-Riva, Montserrat Pidde, Aleksandra Krieg, Michael |
author_facet | Das, Ravi Lin, Li-Chun Català-Castro, Frederic Malaiwong, Nawaphat Sanfeliu-Cerdán, Neus Porta-de-la-Riva, Montserrat Pidde, Aleksandra Krieg, Michael |
author_sort | Das, Ravi |
collection | PubMed |
description | A repetitive gait cycle is an archetypical component within the behavioral repertoire of many animals including humans. It originates from mechanical feedback within proprioceptors to adjust the motor program during locomotion and thus leads to a periodic orbit in a low-dimensional space. Here, we investigate the mechanics, molecules, and neurons responsible for proprioception in Caenorhabditis elegans to gain insight into how mechanosensation shapes the orbital trajectory to a well-defined limit cycle. We used genome editing, force spectroscopy, and multiscale modeling and found that alternating tension and compression with the spectrin network of a single proprioceptor encodes body posture and informs TRP-4/NOMPC and TWK-16/TREK2 homologs of mechanosensitive ion channels during locomotion. In contrast to a widely accepted model of proprioceptive “stretch” reception, we found that proprioceptors activated locally under compressive stresses in-vivo and in-vitro and propose that this property leads to compartmentalized activity within long axons delimited by curvature-dependent mechanical stresses. |
format | Online Article Text |
id | pubmed-8448456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84484562021-09-27 An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity Das, Ravi Lin, Li-Chun Català-Castro, Frederic Malaiwong, Nawaphat Sanfeliu-Cerdán, Neus Porta-de-la-Riva, Montserrat Pidde, Aleksandra Krieg, Michael Sci Adv Neuroscience A repetitive gait cycle is an archetypical component within the behavioral repertoire of many animals including humans. It originates from mechanical feedback within proprioceptors to adjust the motor program during locomotion and thus leads to a periodic orbit in a low-dimensional space. Here, we investigate the mechanics, molecules, and neurons responsible for proprioception in Caenorhabditis elegans to gain insight into how mechanosensation shapes the orbital trajectory to a well-defined limit cycle. We used genome editing, force spectroscopy, and multiscale modeling and found that alternating tension and compression with the spectrin network of a single proprioceptor encodes body posture and informs TRP-4/NOMPC and TWK-16/TREK2 homologs of mechanosensitive ion channels during locomotion. In contrast to a widely accepted model of proprioceptive “stretch” reception, we found that proprioceptors activated locally under compressive stresses in-vivo and in-vitro and propose that this property leads to compartmentalized activity within long axons delimited by curvature-dependent mechanical stresses. American Association for the Advancement of Science 2021-09-17 /pmc/articles/PMC8448456/ /pubmed/34533987 http://dx.doi.org/10.1126/sciadv.abg4617 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Das, Ravi Lin, Li-Chun Català-Castro, Frederic Malaiwong, Nawaphat Sanfeliu-Cerdán, Neus Porta-de-la-Riva, Montserrat Pidde, Aleksandra Krieg, Michael An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity |
title | An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity |
title_full | An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity |
title_fullStr | An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity |
title_full_unstemmed | An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity |
title_short | An asymmetric mechanical code ciphers curvature-dependent proprioceptor activity |
title_sort | asymmetric mechanical code ciphers curvature-dependent proprioceptor activity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448456/ https://www.ncbi.nlm.nih.gov/pubmed/34533987 http://dx.doi.org/10.1126/sciadv.abg4617 |
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