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Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system

Spatio-temporal information about head orientation and movement is fundamental to the sense of balance and motion. Hair cells (HCs) in otolith organs of the vestibular system transduce linear acceleration, including head tilt and vibration. Here, we build a tiltable objective microscope in which an...

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Autores principales: Tanimoto, Masashi, Watakabe, Ikuko, Higashijima, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772181/
https://www.ncbi.nlm.nih.gov/pubmed/36543769
http://dx.doi.org/10.1038/s41467-022-35190-9
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author Tanimoto, Masashi
Watakabe, Ikuko
Higashijima, Shin-ichi
author_facet Tanimoto, Masashi
Watakabe, Ikuko
Higashijima, Shin-ichi
author_sort Tanimoto, Masashi
collection PubMed
description Spatio-temporal information about head orientation and movement is fundamental to the sense of balance and motion. Hair cells (HCs) in otolith organs of the vestibular system transduce linear acceleration, including head tilt and vibration. Here, we build a tiltable objective microscope in which an objective lens and specimen tilt together. With in vivo Ca(2+) imaging of all utricular HCs and ganglion neurons during 360° static tilt and vibration in pitch and roll axes, we reveal the direction- and static/dynamic stimulus-selective topographic responses in larval zebrafish. We find that head vibration is preferentially received by striolar HCs, whereas static tilt is preferentially transduced by extrastriolar HCs. Spatially ordered direction preference in HCs is consistent with hair-bundle polarity and is preserved in ganglion neurons through topographic innervation. Together, these results demonstrate topographically organized selectivity for direction and dynamics of head orientation/movement in the vestibular periphery.
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spelling pubmed-97721812022-12-23 Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system Tanimoto, Masashi Watakabe, Ikuko Higashijima, Shin-ichi Nat Commun Article Spatio-temporal information about head orientation and movement is fundamental to the sense of balance and motion. Hair cells (HCs) in otolith organs of the vestibular system transduce linear acceleration, including head tilt and vibration. Here, we build a tiltable objective microscope in which an objective lens and specimen tilt together. With in vivo Ca(2+) imaging of all utricular HCs and ganglion neurons during 360° static tilt and vibration in pitch and roll axes, we reveal the direction- and static/dynamic stimulus-selective topographic responses in larval zebrafish. We find that head vibration is preferentially received by striolar HCs, whereas static tilt is preferentially transduced by extrastriolar HCs. Spatially ordered direction preference in HCs is consistent with hair-bundle polarity and is preserved in ganglion neurons through topographic innervation. Together, these results demonstrate topographically organized selectivity for direction and dynamics of head orientation/movement in the vestibular periphery. Nature Publishing Group UK 2022-12-21 /pmc/articles/PMC9772181/ /pubmed/36543769 http://dx.doi.org/10.1038/s41467-022-35190-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tanimoto, Masashi
Watakabe, Ikuko
Higashijima, Shin-ichi
Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system
title Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system
title_full Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system
title_fullStr Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system
title_full_unstemmed Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system
title_short Tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system
title_sort tiltable objective microscope visualizes selectivity for head motion direction and dynamics in zebrafish vestibular system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772181/
https://www.ncbi.nlm.nih.gov/pubmed/36543769
http://dx.doi.org/10.1038/s41467-022-35190-9
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