Cargando…

Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion

V2a neurons are a genetically defined cell class that forms a major excitatory descending pathway from the brainstem reticular formation to the spinal cord. Their activation has been linked to the termination of locomotor activity based on broad optogenetic manipulations. However, because of the dif...

Descripción completa

Detalles Bibliográficos
Autores principales: Schwenkgrub, Joanna, Harrell, Evan R., Bathellier, Brice, Bouvier, Julien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821901/
https://www.ncbi.nlm.nih.gov/pubmed/33277252
http://dx.doi.org/10.1126/sciadv.abc6309
_version_ 1783639521348288512
author Schwenkgrub, Joanna
Harrell, Evan R.
Bathellier, Brice
Bouvier, Julien
author_facet Schwenkgrub, Joanna
Harrell, Evan R.
Bathellier, Brice
Bouvier, Julien
author_sort Schwenkgrub, Joanna
collection PubMed
description V2a neurons are a genetically defined cell class that forms a major excitatory descending pathway from the brainstem reticular formation to the spinal cord. Their activation has been linked to the termination of locomotor activity based on broad optogenetic manipulations. However, because of the difficulties involved in accessing brainstem structures for in vivo cell type–specific recordings, V2a neuron function has never been directly observed during natural behaviors. Here, we imaged the activity of V2a neurons using micro-endoscopy in freely moving mice. We find that as many as half of the V2a neurons are excited at locomotion arrest and with low reliability. Other V2a neurons are inhibited at locomotor arrests and/or activated during other behaviors such as locomotion initiation or stationary grooming. Our results establish that V2a neurons not only drive stops as suggested by bulk optogenetics but also are stratified into subpopulations that likely contribute to diverse motor patterns.
format Online
Article
Text
id pubmed-7821901
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-78219012021-01-29 Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion Schwenkgrub, Joanna Harrell, Evan R. Bathellier, Brice Bouvier, Julien Sci Adv Research Articles V2a neurons are a genetically defined cell class that forms a major excitatory descending pathway from the brainstem reticular formation to the spinal cord. Their activation has been linked to the termination of locomotor activity based on broad optogenetic manipulations. However, because of the difficulties involved in accessing brainstem structures for in vivo cell type–specific recordings, V2a neuron function has never been directly observed during natural behaviors. Here, we imaged the activity of V2a neurons using micro-endoscopy in freely moving mice. We find that as many as half of the V2a neurons are excited at locomotion arrest and with low reliability. Other V2a neurons are inhibited at locomotor arrests and/or activated during other behaviors such as locomotion initiation or stationary grooming. Our results establish that V2a neurons not only drive stops as suggested by bulk optogenetics but also are stratified into subpopulations that likely contribute to diverse motor patterns. American Association for the Advancement of Science 2020-12-04 /pmc/articles/PMC7821901/ /pubmed/33277252 http://dx.doi.org/10.1126/sciadv.abc6309 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Schwenkgrub, Joanna
Harrell, Evan R.
Bathellier, Brice
Bouvier, Julien
Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion
title Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion
title_full Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion
title_fullStr Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion
title_full_unstemmed Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion
title_short Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion
title_sort deep imaging in the brainstem reveals functional heterogeneity in v2a neurons controlling locomotion
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821901/
https://www.ncbi.nlm.nih.gov/pubmed/33277252
http://dx.doi.org/10.1126/sciadv.abc6309
work_keys_str_mv AT schwenkgrubjoanna deepimaginginthebrainstemrevealsfunctionalheterogeneityinv2aneuronscontrollinglocomotion
AT harrellevanr deepimaginginthebrainstemrevealsfunctionalheterogeneityinv2aneuronscontrollinglocomotion
AT bathellierbrice deepimaginginthebrainstemrevealsfunctionalheterogeneityinv2aneuronscontrollinglocomotion
AT bouvierjulien deepimaginginthebrainstemrevealsfunctionalheterogeneityinv2aneuronscontrollinglocomotion