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Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio)

Cerebellar dysfunction leads to postural instability. Recent work in freely moving rodents has transformed investigations of cerebellar contributions to posture. However, the combined complexity of terrestrial locomotion and the rodent cerebellum motivate development of new approaches to perturb cer...

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Autores principales: Auer, Franziska, Nardone, Katherine, Matsuda, Koji, Hibi, Masahiko, Schoppik, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515840/
https://www.ncbi.nlm.nih.gov/pubmed/37745506
http://dx.doi.org/10.1101/2023.09.12.557469
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author Auer, Franziska
Nardone, Katherine
Matsuda, Koji
Hibi, Masahiko
Schoppik, David
author_facet Auer, Franziska
Nardone, Katherine
Matsuda, Koji
Hibi, Masahiko
Schoppik, David
author_sort Auer, Franziska
collection PubMed
description Cerebellar dysfunction leads to postural instability. Recent work in freely moving rodents has transformed investigations of cerebellar contributions to posture. However, the combined complexity of terrestrial locomotion and the rodent cerebellum motivate development of new approaches to perturb cerebellar function in simpler vertebrates. Here, we used a powerful chemogenetic tool (TRPV1/capsaicin) to define the role of Purkinje cells – the output neurons of the cerebellar cortex – as larval zebrafish swam freely in depth. We achieved both bidirectional control (activation and ablation) of Purkinje cells while performing quantitative high-throughput assessment of posture and locomotion. Activation disrupted postural control in the pitch (nose-up/nose-down) axis. Similarly, ablations disrupted pitch-axis posture and fin-body coordination responsible for climbs. Postural disruption was more pronounced in older larvae, offering a window into emergent roles for the developing cerebellum in the control of posture. Finally, we found that activity in Purkinje cells could individually and collectively encode tilt direction, a key feature of postural control neurons. Our findings delineate an expected role for the cerebellum in postural control and vestibular sensation in larval zebrafish, establishing the validity of TRPV1/capsaicin-mediated perturbations in a simple, genetically-tractable vertebrate. Moreover, by comparing the contributions of Purkinje cell ablations to posture in time, we uncover signatures of emerging cerebellar control of posture across early development. This work takes a major step towards understanding an ancestral role of the cerebellum in regulating postural maturation.
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spelling pubmed-105158402023-09-23 Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio) Auer, Franziska Nardone, Katherine Matsuda, Koji Hibi, Masahiko Schoppik, David bioRxiv Article Cerebellar dysfunction leads to postural instability. Recent work in freely moving rodents has transformed investigations of cerebellar contributions to posture. However, the combined complexity of terrestrial locomotion and the rodent cerebellum motivate development of new approaches to perturb cerebellar function in simpler vertebrates. Here, we used a powerful chemogenetic tool (TRPV1/capsaicin) to define the role of Purkinje cells – the output neurons of the cerebellar cortex – as larval zebrafish swam freely in depth. We achieved both bidirectional control (activation and ablation) of Purkinje cells while performing quantitative high-throughput assessment of posture and locomotion. Activation disrupted postural control in the pitch (nose-up/nose-down) axis. Similarly, ablations disrupted pitch-axis posture and fin-body coordination responsible for climbs. Postural disruption was more pronounced in older larvae, offering a window into emergent roles for the developing cerebellum in the control of posture. Finally, we found that activity in Purkinje cells could individually and collectively encode tilt direction, a key feature of postural control neurons. Our findings delineate an expected role for the cerebellum in postural control and vestibular sensation in larval zebrafish, establishing the validity of TRPV1/capsaicin-mediated perturbations in a simple, genetically-tractable vertebrate. Moreover, by comparing the contributions of Purkinje cell ablations to posture in time, we uncover signatures of emerging cerebellar control of posture across early development. This work takes a major step towards understanding an ancestral role of the cerebellum in regulating postural maturation. Cold Spring Harbor Laboratory 2023-09-14 /pmc/articles/PMC10515840/ /pubmed/37745506 http://dx.doi.org/10.1101/2023.09.12.557469 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Auer, Franziska
Nardone, Katherine
Matsuda, Koji
Hibi, Masahiko
Schoppik, David
Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio)
title Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio)
title_full Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio)
title_fullStr Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio)
title_full_unstemmed Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio)
title_short Purkinje Cells Control Posture in Larval Zebrafish (Danio rerio)
title_sort purkinje cells control posture in larval zebrafish (danio rerio)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515840/
https://www.ncbi.nlm.nih.gov/pubmed/37745506
http://dx.doi.org/10.1101/2023.09.12.557469
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