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Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization
Across the nervous system, neurons with similar attributes are topographically organized. This topography reflects developmental pressures. Oddly, vestibular (balance) nuclei are thought to be disorganized. By measuring activity in birthdated neurons, we revealed a functional map within the central...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089979/ https://www.ncbi.nlm.nih.gov/pubmed/36924768 http://dx.doi.org/10.1016/j.cub.2023.02.048 |
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author | Goldblatt, Dena Huang, Stephanie Greaney, Marie R. Hamling, Kyla R. Voleti, Venkatakaushik Perez-Campos, Citlali Patel, Kripa B. Li, Wenze Hillman, Elizabeth M.C. Bagnall, Martha W. Schoppik, David |
author_facet | Goldblatt, Dena Huang, Stephanie Greaney, Marie R. Hamling, Kyla R. Voleti, Venkatakaushik Perez-Campos, Citlali Patel, Kripa B. Li, Wenze Hillman, Elizabeth M.C. Bagnall, Martha W. Schoppik, David |
author_sort | Goldblatt, Dena |
collection | PubMed |
description | Across the nervous system, neurons with similar attributes are topographically organized. This topography reflects developmental pressures. Oddly, vestibular (balance) nuclei are thought to be disorganized. By measuring activity in birthdated neurons, we revealed a functional map within the central vestibular projection nucleus that stabilizes gaze in the larval zebrafish. We first discovered that both somatic position and stimulus selectivity follow projection neuron birthdate. Next, with electron microscopy and loss-of-function assays, we found that patterns of peripheral innervation to projection neurons were similarly organized by birthdate. Finally, birthdate revealed spatial patterns of axonal arborization and synapse formation to projection neuron outputs. Collectively, we find that development reveals previously hidden organization to the input, processing, and output layers of a highly conserved vertebrate sensorimotor circuit. The spatial and temporal attributes we uncover constrain the developmental mechanisms that may specify the fate, function, and organization of vestibulo-ocular reflex neurons. More broadly, our data suggest that, like invertebrates, temporal mechanisms may assemble vertebrate sensorimotor architecture. |
format | Online Article Text |
id | pubmed-10089979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-100899792023-04-12 Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization Goldblatt, Dena Huang, Stephanie Greaney, Marie R. Hamling, Kyla R. Voleti, Venkatakaushik Perez-Campos, Citlali Patel, Kripa B. Li, Wenze Hillman, Elizabeth M.C. Bagnall, Martha W. Schoppik, David Curr Biol Article Across the nervous system, neurons with similar attributes are topographically organized. This topography reflects developmental pressures. Oddly, vestibular (balance) nuclei are thought to be disorganized. By measuring activity in birthdated neurons, we revealed a functional map within the central vestibular projection nucleus that stabilizes gaze in the larval zebrafish. We first discovered that both somatic position and stimulus selectivity follow projection neuron birthdate. Next, with electron microscopy and loss-of-function assays, we found that patterns of peripheral innervation to projection neurons were similarly organized by birthdate. Finally, birthdate revealed spatial patterns of axonal arborization and synapse formation to projection neuron outputs. Collectively, we find that development reveals previously hidden organization to the input, processing, and output layers of a highly conserved vertebrate sensorimotor circuit. The spatial and temporal attributes we uncover constrain the developmental mechanisms that may specify the fate, function, and organization of vestibulo-ocular reflex neurons. More broadly, our data suggest that, like invertebrates, temporal mechanisms may assemble vertebrate sensorimotor architecture. 2023-04-10 2023-03-15 /pmc/articles/PMC10089979/ /pubmed/36924768 http://dx.doi.org/10.1016/j.cub.2023.02.048 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Goldblatt, Dena Huang, Stephanie Greaney, Marie R. Hamling, Kyla R. Voleti, Venkatakaushik Perez-Campos, Citlali Patel, Kripa B. Li, Wenze Hillman, Elizabeth M.C. Bagnall, Martha W. Schoppik, David Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization |
title | Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization |
title_full | Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization |
title_fullStr | Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization |
title_full_unstemmed | Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization |
title_short | Neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization |
title_sort | neuronal birthdate reveals topography in a vestibular brainstem circuit for gaze stabilization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089979/ https://www.ncbi.nlm.nih.gov/pubmed/36924768 http://dx.doi.org/10.1016/j.cub.2023.02.048 |
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