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Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord

Cerebrospinal fluid-contacting neurons (CSF-cNs) are enigmatic mechano- or chemosensory cells lying along the central canal of the spinal cord. Recent studies in zebrafish larvae and lampreys have shown that CSF-cNs control postures and movements via spinal connections. However, the structures, conn...

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Autores principales: Nakamura, Yuka, Kurabe, Miyuki, Matsumoto, Mami, Sato, Tokiharu, Miyashita, Satoshi, Hoshina, Kana, Kamiya, Yoshinori, Tainaka, Kazuki, Matsuzawa, Hitoshi, Ohno, Nobuhiko, Ueno, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9943067/
https://www.ncbi.nlm.nih.gov/pubmed/36805807
http://dx.doi.org/10.7554/eLife.83108
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author Nakamura, Yuka
Kurabe, Miyuki
Matsumoto, Mami
Sato, Tokiharu
Miyashita, Satoshi
Hoshina, Kana
Kamiya, Yoshinori
Tainaka, Kazuki
Matsuzawa, Hitoshi
Ohno, Nobuhiko
Ueno, Masaki
author_facet Nakamura, Yuka
Kurabe, Miyuki
Matsumoto, Mami
Sato, Tokiharu
Miyashita, Satoshi
Hoshina, Kana
Kamiya, Yoshinori
Tainaka, Kazuki
Matsuzawa, Hitoshi
Ohno, Nobuhiko
Ueno, Masaki
author_sort Nakamura, Yuka
collection PubMed
description Cerebrospinal fluid-contacting neurons (CSF-cNs) are enigmatic mechano- or chemosensory cells lying along the central canal of the spinal cord. Recent studies in zebrafish larvae and lampreys have shown that CSF-cNs control postures and movements via spinal connections. However, the structures, connectivity, and functions in mammals remain largely unknown. Here we developed a method to genetically target mouse CSF-cNs that highlighted structural connections and functions. We first found that intracerebroventricular injection of adeno-associated virus with a neuron-specific promoter and Pkd2l1-Cre mice specifically labeled CSF-cNs. Single-cell labeling of 71 CSF-cNs revealed rostral axon extensions of over 1800 μm in unmyelinated bundles in the ventral funiculus and terminated on CSF-cNs to form a recurrent circuitry, which was further determined by serial electron microscopy and electrophysiology. CSF-cNs were also found to connect with axial motor neurons and premotor interneurons around the central canal and within the axon bundles. Chemogenetic CSF-cNs inactivation reduced speed and step frequency during treadmill locomotion. Our data revealed the basic structures and connections of mouse CSF-cNs to control spinal motor circuits for proper locomotion. The versatile methods developed in this study will contribute to further understanding of CSF-cN functions in mammals.
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spelling pubmed-99430672023-02-22 Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord Nakamura, Yuka Kurabe, Miyuki Matsumoto, Mami Sato, Tokiharu Miyashita, Satoshi Hoshina, Kana Kamiya, Yoshinori Tainaka, Kazuki Matsuzawa, Hitoshi Ohno, Nobuhiko Ueno, Masaki eLife Neuroscience Cerebrospinal fluid-contacting neurons (CSF-cNs) are enigmatic mechano- or chemosensory cells lying along the central canal of the spinal cord. Recent studies in zebrafish larvae and lampreys have shown that CSF-cNs control postures and movements via spinal connections. However, the structures, connectivity, and functions in mammals remain largely unknown. Here we developed a method to genetically target mouse CSF-cNs that highlighted structural connections and functions. We first found that intracerebroventricular injection of adeno-associated virus with a neuron-specific promoter and Pkd2l1-Cre mice specifically labeled CSF-cNs. Single-cell labeling of 71 CSF-cNs revealed rostral axon extensions of over 1800 μm in unmyelinated bundles in the ventral funiculus and terminated on CSF-cNs to form a recurrent circuitry, which was further determined by serial electron microscopy and electrophysiology. CSF-cNs were also found to connect with axial motor neurons and premotor interneurons around the central canal and within the axon bundles. Chemogenetic CSF-cNs inactivation reduced speed and step frequency during treadmill locomotion. Our data revealed the basic structures and connections of mouse CSF-cNs to control spinal motor circuits for proper locomotion. The versatile methods developed in this study will contribute to further understanding of CSF-cN functions in mammals. eLife Sciences Publications, Ltd 2023-02-21 /pmc/articles/PMC9943067/ /pubmed/36805807 http://dx.doi.org/10.7554/eLife.83108 Text en © 2023, Nakamura et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Nakamura, Yuka
Kurabe, Miyuki
Matsumoto, Mami
Sato, Tokiharu
Miyashita, Satoshi
Hoshina, Kana
Kamiya, Yoshinori
Tainaka, Kazuki
Matsuzawa, Hitoshi
Ohno, Nobuhiko
Ueno, Masaki
Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord
title Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord
title_full Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord
title_fullStr Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord
title_full_unstemmed Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord
title_short Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord
title_sort cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9943067/
https://www.ncbi.nlm.nih.gov/pubmed/36805807
http://dx.doi.org/10.7554/eLife.83108
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