Cargando…

Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila

The sense of proprioception is mediated by internal mechanosensory neurons that detect joint position and movement. To support a diverse range of functions, from stabilizing posture to coordinating movements, proprioceptive feedback to limb motor control circuits must be tuned in a context-dependent...

Descripción completa

Detalles Bibliográficos
Autores principales: Dallmann, Chris J., Agrawal, Sweta, Cook, Andrew, Brunton, Bingni W., Tuthill, John C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634730/
https://www.ncbi.nlm.nih.gov/pubmed/37961558
http://dx.doi.org/10.1101/2023.10.20.563322
_version_ 1785146231501094912
author Dallmann, Chris J.
Agrawal, Sweta
Cook, Andrew
Brunton, Bingni W.
Tuthill, John C.
author_facet Dallmann, Chris J.
Agrawal, Sweta
Cook, Andrew
Brunton, Bingni W.
Tuthill, John C.
author_sort Dallmann, Chris J.
collection PubMed
description The sense of proprioception is mediated by internal mechanosensory neurons that detect joint position and movement. To support a diverse range of functions, from stabilizing posture to coordinating movements, proprioceptive feedback to limb motor control circuits must be tuned in a context-dependent manner. How proprioceptive feedback signals are tuned to match behavioral demands remains poorly understood. Using calcium imaging in behaving Drosophila, we find that the axons of position-encoding leg proprioceptors are active across behaviors, whereas the axons of movement-encoding leg proprioceptors are suppressed during walking and grooming. Using connectomics, we identify a specific class of interneurons that provide GABAergic presynaptic inhibition to the axons of movement-encoding proprioceptors. These interneurons are active during self-generated but not passive leg movements and receive input from descending neurons, suggesting they are driven by predictions of leg movement originating in the brain. Predictively suppressing expected proprioceptive feedback provides a mechanism to attenuate reflexes that would otherwise interfere with voluntary movement.
format Online
Article
Text
id pubmed-10634730
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-106347302023-11-13 Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila Dallmann, Chris J. Agrawal, Sweta Cook, Andrew Brunton, Bingni W. Tuthill, John C. bioRxiv Article The sense of proprioception is mediated by internal mechanosensory neurons that detect joint position and movement. To support a diverse range of functions, from stabilizing posture to coordinating movements, proprioceptive feedback to limb motor control circuits must be tuned in a context-dependent manner. How proprioceptive feedback signals are tuned to match behavioral demands remains poorly understood. Using calcium imaging in behaving Drosophila, we find that the axons of position-encoding leg proprioceptors are active across behaviors, whereas the axons of movement-encoding leg proprioceptors are suppressed during walking and grooming. Using connectomics, we identify a specific class of interneurons that provide GABAergic presynaptic inhibition to the axons of movement-encoding proprioceptors. These interneurons are active during self-generated but not passive leg movements and receive input from descending neurons, suggesting they are driven by predictions of leg movement originating in the brain. Predictively suppressing expected proprioceptive feedback provides a mechanism to attenuate reflexes that would otherwise interfere with voluntary movement. Cold Spring Harbor Laboratory 2023-10-23 /pmc/articles/PMC10634730/ /pubmed/37961558 http://dx.doi.org/10.1101/2023.10.20.563322 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Dallmann, Chris J.
Agrawal, Sweta
Cook, Andrew
Brunton, Bingni W.
Tuthill, John C.
Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila
title Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila
title_full Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila
title_fullStr Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila
title_full_unstemmed Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila
title_short Presynaptic inhibition selectively suppresses leg proprioception in behaving Drosophila
title_sort presynaptic inhibition selectively suppresses leg proprioception in behaving drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634730/
https://www.ncbi.nlm.nih.gov/pubmed/37961558
http://dx.doi.org/10.1101/2023.10.20.563322
work_keys_str_mv AT dallmannchrisj presynapticinhibitionselectivelysuppresseslegproprioceptioninbehavingdrosophila
AT agrawalsweta presynapticinhibitionselectivelysuppresseslegproprioceptioninbehavingdrosophila
AT cookandrew presynapticinhibitionselectivelysuppresseslegproprioceptioninbehavingdrosophila
AT bruntonbingniw presynapticinhibitionselectivelysuppresseslegproprioceptioninbehavingdrosophila
AT tuthilljohnc presynapticinhibitionselectivelysuppresseslegproprioceptioninbehavingdrosophila