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Organization of the gravity-sensing system in zebrafish
Motor circuits develop in sequence from those governing fast movements to those governing slow. Here we examine whether upstream sensory circuits are organized by similar principles. Using serial-section electron microscopy in larval zebrafish, we generated a complete map of the gravity-sensing (utr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420129/ https://www.ncbi.nlm.nih.gov/pubmed/36030280 http://dx.doi.org/10.1038/s41467-022-32824-w |
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author | Liu, Zhikai Hildebrand, David G. C. Morgan, Joshua L. Jia, Yizhen Slimmon, Nicholas Bagnall, Martha W. |
author_facet | Liu, Zhikai Hildebrand, David G. C. Morgan, Joshua L. Jia, Yizhen Slimmon, Nicholas Bagnall, Martha W. |
author_sort | Liu, Zhikai |
collection | PubMed |
description | Motor circuits develop in sequence from those governing fast movements to those governing slow. Here we examine whether upstream sensory circuits are organized by similar principles. Using serial-section electron microscopy in larval zebrafish, we generated a complete map of the gravity-sensing (utricular) system spanning from the inner ear to the brainstem. We find that both sensory tuning and developmental sequence are organizing principles of vestibular topography. Patterned rostrocaudal innervation from hair cells to afferents creates an anatomically inferred directional tuning map in the utricular ganglion, forming segregated pathways for rostral and caudal tilt. Furthermore, the mediolateral axis of the ganglion is linked to both developmental sequence and neuronal temporal dynamics. Early-born pathways carrying phasic information preferentially excite fast escape circuits, whereas later-born pathways carrying tonic signals excite slower postural and oculomotor circuits. These results demonstrate that vestibular circuits are organized by tuning direction and dynamics, aligning them with downstream motor circuits and behaviors. |
format | Online Article Text |
id | pubmed-9420129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94201292022-08-29 Organization of the gravity-sensing system in zebrafish Liu, Zhikai Hildebrand, David G. C. Morgan, Joshua L. Jia, Yizhen Slimmon, Nicholas Bagnall, Martha W. Nat Commun Article Motor circuits develop in sequence from those governing fast movements to those governing slow. Here we examine whether upstream sensory circuits are organized by similar principles. Using serial-section electron microscopy in larval zebrafish, we generated a complete map of the gravity-sensing (utricular) system spanning from the inner ear to the brainstem. We find that both sensory tuning and developmental sequence are organizing principles of vestibular topography. Patterned rostrocaudal innervation from hair cells to afferents creates an anatomically inferred directional tuning map in the utricular ganglion, forming segregated pathways for rostral and caudal tilt. Furthermore, the mediolateral axis of the ganglion is linked to both developmental sequence and neuronal temporal dynamics. Early-born pathways carrying phasic information preferentially excite fast escape circuits, whereas later-born pathways carrying tonic signals excite slower postural and oculomotor circuits. These results demonstrate that vestibular circuits are organized by tuning direction and dynamics, aligning them with downstream motor circuits and behaviors. Nature Publishing Group UK 2022-08-27 /pmc/articles/PMC9420129/ /pubmed/36030280 http://dx.doi.org/10.1038/s41467-022-32824-w 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 Liu, Zhikai Hildebrand, David G. C. Morgan, Joshua L. Jia, Yizhen Slimmon, Nicholas Bagnall, Martha W. Organization of the gravity-sensing system in zebrafish |
title | Organization of the gravity-sensing system in zebrafish |
title_full | Organization of the gravity-sensing system in zebrafish |
title_fullStr | Organization of the gravity-sensing system in zebrafish |
title_full_unstemmed | Organization of the gravity-sensing system in zebrafish |
title_short | Organization of the gravity-sensing system in zebrafish |
title_sort | organization of the gravity-sensing system in zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420129/ https://www.ncbi.nlm.nih.gov/pubmed/36030280 http://dx.doi.org/10.1038/s41467-022-32824-w |
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