Cargando…
Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region
A key function of the mesencephalic locomotor region (MLR) is to control the speed of forward symmetrical locomotor movements. However, the ability of freely moving mammals to integrate environmental cues to brake and turn during MLR stimulation is poorly documented. Here, we investigated whether fr...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062873/ https://www.ncbi.nlm.nih.gov/pubmed/33897379 http://dx.doi.org/10.3389/fncir.2021.639900 |
_version_ | 1783681854181736448 |
---|---|
author | van der Zouwen, Cornelis Immanuel Boutin, Joël Fougère, Maxime Flaive, Aurélie Vivancos, Mélanie Santuz, Alessandro Akay, Turgay Sarret, Philippe Ryczko, Dimitri |
author_facet | van der Zouwen, Cornelis Immanuel Boutin, Joël Fougère, Maxime Flaive, Aurélie Vivancos, Mélanie Santuz, Alessandro Akay, Turgay Sarret, Philippe Ryczko, Dimitri |
author_sort | van der Zouwen, Cornelis Immanuel |
collection | PubMed |
description | A key function of the mesencephalic locomotor region (MLR) is to control the speed of forward symmetrical locomotor movements. However, the ability of freely moving mammals to integrate environmental cues to brake and turn during MLR stimulation is poorly documented. Here, we investigated whether freely behaving mice could brake or turn, based on environmental cues during MLR stimulation. We photostimulated the cuneiform nucleus (part of the MLR) in mice expressing channelrhodopsin in Vglut2-positive neurons in a Cre-dependent manner (Vglut2-ChR2-EYFP) using optogenetics. We detected locomotor movements using deep learning. We used patch-clamp recordings to validate the functional expression of channelrhodopsin and neuroanatomy to visualize the stimulation sites. In the linear corridor, gait diagram and limb kinematics were similar during spontaneous and optogenetic-evoked locomotion. In the open-field arena, optogenetic stimulation of the MLR evoked locomotion, and increasing laser power increased locomotor speed. Mice could brake and make sharp turns (~90°) when approaching a corner during MLR stimulation in the open-field arena. The speed during the turn was scaled with the speed before the turn, and with the turn angle. Patch-clamp recordings in Vglut2-ChR2-EYFP mice show that blue light evoked short-latency spiking in MLR neurons. Our results strengthen the idea that different brainstem neurons convey braking/turning and MLR speed commands in mammals. Our study also shows that Vglut2-positive neurons of the cuneiform nucleus are a relevant target to increase locomotor activity without impeding the ability to brake and turn when approaching obstacles, thus ensuring smooth and adaptable navigation. Our observations may have clinical relevance since cuneiform nucleus stimulation is increasingly considered to improve locomotion function in pathological states such as Parkinson’s disease, spinal cord injury, or stroke. |
format | Online Article Text |
id | pubmed-8062873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80628732021-04-24 Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region van der Zouwen, Cornelis Immanuel Boutin, Joël Fougère, Maxime Flaive, Aurélie Vivancos, Mélanie Santuz, Alessandro Akay, Turgay Sarret, Philippe Ryczko, Dimitri Front Neural Circuits Neuroscience A key function of the mesencephalic locomotor region (MLR) is to control the speed of forward symmetrical locomotor movements. However, the ability of freely moving mammals to integrate environmental cues to brake and turn during MLR stimulation is poorly documented. Here, we investigated whether freely behaving mice could brake or turn, based on environmental cues during MLR stimulation. We photostimulated the cuneiform nucleus (part of the MLR) in mice expressing channelrhodopsin in Vglut2-positive neurons in a Cre-dependent manner (Vglut2-ChR2-EYFP) using optogenetics. We detected locomotor movements using deep learning. We used patch-clamp recordings to validate the functional expression of channelrhodopsin and neuroanatomy to visualize the stimulation sites. In the linear corridor, gait diagram and limb kinematics were similar during spontaneous and optogenetic-evoked locomotion. In the open-field arena, optogenetic stimulation of the MLR evoked locomotion, and increasing laser power increased locomotor speed. Mice could brake and make sharp turns (~90°) when approaching a corner during MLR stimulation in the open-field arena. The speed during the turn was scaled with the speed before the turn, and with the turn angle. Patch-clamp recordings in Vglut2-ChR2-EYFP mice show that blue light evoked short-latency spiking in MLR neurons. Our results strengthen the idea that different brainstem neurons convey braking/turning and MLR speed commands in mammals. Our study also shows that Vglut2-positive neurons of the cuneiform nucleus are a relevant target to increase locomotor activity without impeding the ability to brake and turn when approaching obstacles, thus ensuring smooth and adaptable navigation. Our observations may have clinical relevance since cuneiform nucleus stimulation is increasingly considered to improve locomotion function in pathological states such as Parkinson’s disease, spinal cord injury, or stroke. Frontiers Media S.A. 2021-04-09 /pmc/articles/PMC8062873/ /pubmed/33897379 http://dx.doi.org/10.3389/fncir.2021.639900 Text en Copyright © 2021 van der Zouwen, Boutin, Fougère, Flaive, Vivancos, Santuz, Akay, Sarret and Ryczko. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience van der Zouwen, Cornelis Immanuel Boutin, Joël Fougère, Maxime Flaive, Aurélie Vivancos, Mélanie Santuz, Alessandro Akay, Turgay Sarret, Philippe Ryczko, Dimitri Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region |
title | Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region |
title_full | Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region |
title_fullStr | Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region |
title_full_unstemmed | Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region |
title_short | Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region |
title_sort | freely behaving mice can brake and turn during optogenetic stimulation of the mesencephalic locomotor region |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062873/ https://www.ncbi.nlm.nih.gov/pubmed/33897379 http://dx.doi.org/10.3389/fncir.2021.639900 |
work_keys_str_mv | AT vanderzouwencornelisimmanuel freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT boutinjoel freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT fougeremaxime freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT flaiveaurelie freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT vivancosmelanie freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT santuzalessandro freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT akayturgay freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT sarretphilippe freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion AT ryczkodimitri freelybehavingmicecanbrakeandturnduringoptogeneticstimulationofthemesencephaliclocomotorregion |