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Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish

The vestibular apparatus provides animals with postural and movement-related information that is essential to adequately execute numerous sensorimotor tasks. In order to activate this sensory system in a physiological manner, one needs to macroscopically rotate or translate the animal’s head, which...

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Autores principales: Migault, Geoffrey, van der Plas, Thijs L., Trentesaux, Hugo, Panier, Thomas, Candelier, Raphaël, Proville, Rémi, Englitz, Bernhard, Debrégeas, Georges, Bormuth, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288061/
https://www.ncbi.nlm.nih.gov/pubmed/30449666
http://dx.doi.org/10.1016/j.cub.2018.10.017
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author Migault, Geoffrey
van der Plas, Thijs L.
Trentesaux, Hugo
Panier, Thomas
Candelier, Raphaël
Proville, Rémi
Englitz, Bernhard
Debrégeas, Georges
Bormuth, Volker
author_facet Migault, Geoffrey
van der Plas, Thijs L.
Trentesaux, Hugo
Panier, Thomas
Candelier, Raphaël
Proville, Rémi
Englitz, Bernhard
Debrégeas, Georges
Bormuth, Volker
author_sort Migault, Geoffrey
collection PubMed
description The vestibular apparatus provides animals with postural and movement-related information that is essential to adequately execute numerous sensorimotor tasks. In order to activate this sensory system in a physiological manner, one needs to macroscopically rotate or translate the animal’s head, which in turn renders simultaneous neural recordings highly challenging. Here we report on a novel miniaturized, light-sheet microscope that can be dynamically co-rotated with a head-restrained zebrafish larva, enabling controlled vestibular stimulation. The mechanical rigidity of the microscope allows one to perform whole-brain functional imaging with state-of-the-art resolution and signal-to-noise ratio while imposing up to 25° in angular position and 6,000°/s(2) in rotational acceleration. We illustrate the potential of this novel setup by producing the first whole-brain response maps to sinusoidal and stepwise vestibular stimulation. The responsive population spans multiple brain areas and displays bilateral symmetry, and its organization is highly stereotypic across individuals. Using Fourier and regression analysis, we identified three major functional clusters that exhibit well-defined phasic and tonic response patterns to vestibular stimulation. Our rotatable light-sheet microscope provides a unique tool for systematically studying vestibular processing in the vertebrate brain and extends the potential of virtual-reality systems to explore complex multisensory and motor integration during simulated 3D navigation.
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spelling pubmed-62880612018-12-19 Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish Migault, Geoffrey van der Plas, Thijs L. Trentesaux, Hugo Panier, Thomas Candelier, Raphaël Proville, Rémi Englitz, Bernhard Debrégeas, Georges Bormuth, Volker Curr Biol Article The vestibular apparatus provides animals with postural and movement-related information that is essential to adequately execute numerous sensorimotor tasks. In order to activate this sensory system in a physiological manner, one needs to macroscopically rotate or translate the animal’s head, which in turn renders simultaneous neural recordings highly challenging. Here we report on a novel miniaturized, light-sheet microscope that can be dynamically co-rotated with a head-restrained zebrafish larva, enabling controlled vestibular stimulation. The mechanical rigidity of the microscope allows one to perform whole-brain functional imaging with state-of-the-art resolution and signal-to-noise ratio while imposing up to 25° in angular position and 6,000°/s(2) in rotational acceleration. We illustrate the potential of this novel setup by producing the first whole-brain response maps to sinusoidal and stepwise vestibular stimulation. The responsive population spans multiple brain areas and displays bilateral symmetry, and its organization is highly stereotypic across individuals. Using Fourier and regression analysis, we identified three major functional clusters that exhibit well-defined phasic and tonic response patterns to vestibular stimulation. Our rotatable light-sheet microscope provides a unique tool for systematically studying vestibular processing in the vertebrate brain and extends the potential of virtual-reality systems to explore complex multisensory and motor integration during simulated 3D navigation. Cell Press 2018-12-03 /pmc/articles/PMC6288061/ /pubmed/30449666 http://dx.doi.org/10.1016/j.cub.2018.10.017 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Migault, Geoffrey
van der Plas, Thijs L.
Trentesaux, Hugo
Panier, Thomas
Candelier, Raphaël
Proville, Rémi
Englitz, Bernhard
Debrégeas, Georges
Bormuth, Volker
Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish
title Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish
title_full Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish
title_fullStr Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish
title_full_unstemmed Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish
title_short Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish
title_sort whole-brain calcium imaging during physiological vestibular stimulation in larval zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288061/
https://www.ncbi.nlm.nih.gov/pubmed/30449666
http://dx.doi.org/10.1016/j.cub.2018.10.017
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