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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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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 |
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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 |
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