Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Das, Ravi, Lin, Li-Chun, Català-Castro, Frederic, Malaiwong, Nawaphat, Sanfeliu-Cerdán, Neus, Porta-de-la-Riva, Montserrat, Pidde, Aleksandra, Krieg, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
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
_version_ 1784569246067458048
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
work_keys_str_mv AT dasravi anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT linlichun anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT catalacastrofrederic anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT malaiwongnawaphat anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT sanfeliucerdanneus anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT portadelarivamontserrat anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT piddealeksandra anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT kriegmichael anasymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT dasravi asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT linlichun asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT catalacastrofrederic asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT malaiwongnawaphat asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT sanfeliucerdanneus asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT portadelarivamontserrat asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT piddealeksandra asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity
AT kriegmichael asymmetricmechanicalcodecipherscurvaturedependentproprioceptoractivity