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Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy

Proprioceptors provide feedback about body position that is essential for coordinated movement. Proprioceptive sensing of the position of rigid joints has been described in detail in several systems; however, it is not known how animals with a flexible skeleton encode their body positions. Understan...

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Autores principales: Vaadia, Rebecca D., Li, Wenze, Voleti, Venkatakaushik, Singhania, Aditi, Hillman, Elizabeth M.C., Grueber, Wesley B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624193/
https://www.ncbi.nlm.nih.gov/pubmed/30853438
http://dx.doi.org/10.1016/j.cub.2019.01.060
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author Vaadia, Rebecca D.
Li, Wenze
Voleti, Venkatakaushik
Singhania, Aditi
Hillman, Elizabeth M.C.
Grueber, Wesley B.
author_facet Vaadia, Rebecca D.
Li, Wenze
Voleti, Venkatakaushik
Singhania, Aditi
Hillman, Elizabeth M.C.
Grueber, Wesley B.
author_sort Vaadia, Rebecca D.
collection PubMed
description Proprioceptors provide feedback about body position that is essential for coordinated movement. Proprioceptive sensing of the position of rigid joints has been described in detail in several systems; however, it is not known how animals with a flexible skeleton encode their body positions. Understanding how diverse larval body positions are dynamically encoded requires knowledge of proprioceptor activity patterns in vivo during natural movement. Here we used high-speed volumetric swept confocally aligned planar excitation (SCAPE) microscopy in crawling Drosophila larvae to simultaneously track the position, deformation, and intracellular calcium activity of their multidendritic proprioceptors. Most proprioceptive neurons were found to activate during segment contraction, although one subtype was activated by extension. During cycles of segment contraction and extension, different proprioceptor types exhibited sequential activity, providing a continuum of position encoding during all phases of crawling. This sequential activity was related to the dynamics of each neuron’s terminal processes, and could endow each proprioceptor with a specific role in monitoring different aspects of body-wall deformation. We demonstrate this deformation encoding both during progression of contraction waves during locomotion as well as during less stereotyped, asymmetric exploration behavior. Our results provide powerful new insights into the body-wide neuronal dynamics of the proprioceptive system in crawling Drosophila, and demonstrate the utility of our SCAPE microscopy approach for characterization of neural encoding throughout the nervous system of a freely behaving animal.
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spelling pubmed-66241932020-03-18 Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy Vaadia, Rebecca D. Li, Wenze Voleti, Venkatakaushik Singhania, Aditi Hillman, Elizabeth M.C. Grueber, Wesley B. Curr Biol Article Proprioceptors provide feedback about body position that is essential for coordinated movement. Proprioceptive sensing of the position of rigid joints has been described in detail in several systems; however, it is not known how animals with a flexible skeleton encode their body positions. Understanding how diverse larval body positions are dynamically encoded requires knowledge of proprioceptor activity patterns in vivo during natural movement. Here we used high-speed volumetric swept confocally aligned planar excitation (SCAPE) microscopy in crawling Drosophila larvae to simultaneously track the position, deformation, and intracellular calcium activity of their multidendritic proprioceptors. Most proprioceptive neurons were found to activate during segment contraction, although one subtype was activated by extension. During cycles of segment contraction and extension, different proprioceptor types exhibited sequential activity, providing a continuum of position encoding during all phases of crawling. This sequential activity was related to the dynamics of each neuron’s terminal processes, and could endow each proprioceptor with a specific role in monitoring different aspects of body-wall deformation. We demonstrate this deformation encoding both during progression of contraction waves during locomotion as well as during less stereotyped, asymmetric exploration behavior. Our results provide powerful new insights into the body-wide neuronal dynamics of the proprioceptive system in crawling Drosophila, and demonstrate the utility of our SCAPE microscopy approach for characterization of neural encoding throughout the nervous system of a freely behaving animal. 2019-03-07 2019-03-18 /pmc/articles/PMC6624193/ /pubmed/30853438 http://dx.doi.org/10.1016/j.cub.2019.01.060 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vaadia, Rebecca D.
Li, Wenze
Voleti, Venkatakaushik
Singhania, Aditi
Hillman, Elizabeth M.C.
Grueber, Wesley B.
Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy
title Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy
title_full Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy
title_fullStr Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy
title_full_unstemmed Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy
title_short Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy
title_sort characterization of proprioceptive system dynamics in behaving drosophila larvae using high-speed volumetric microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624193/
https://www.ncbi.nlm.nih.gov/pubmed/30853438
http://dx.doi.org/10.1016/j.cub.2019.01.060
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