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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...

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Autores principales: Liu, Zhikai, Hildebrand, David G. C., Morgan, Joshua L., Jia, Yizhen, Slimmon, Nicholas, Bagnall, Martha W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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