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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
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.
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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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