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Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration

Visual information reaches cortex via the thalamic dorsal lateral geniculate nucleus (dLGN). dLGN activity is modulated by global sleep/wake states and arousal, indicating that it is not simply a passive relay station. However, its potential for more specific visuomotor integration is largely unexpl...

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Autores principales: Orlowska-Feuer, Patrycja, Ebrahimi, Aghileh S., Zippo, Antonio G., Petersen, Rasmus S., Lucas, Robert J., Storchi, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616738/
https://www.ncbi.nlm.nih.gov/pubmed/35973431
http://dx.doi.org/10.1016/j.cub.2022.07.049
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author Orlowska-Feuer, Patrycja
Ebrahimi, Aghileh S.
Zippo, Antonio G.
Petersen, Rasmus S.
Lucas, Robert J.
Storchi, Riccardo
author_facet Orlowska-Feuer, Patrycja
Ebrahimi, Aghileh S.
Zippo, Antonio G.
Petersen, Rasmus S.
Lucas, Robert J.
Storchi, Riccardo
author_sort Orlowska-Feuer, Patrycja
collection PubMed
description Visual information reaches cortex via the thalamic dorsal lateral geniculate nucleus (dLGN). dLGN activity is modulated by global sleep/wake states and arousal, indicating that it is not simply a passive relay station. However, its potential for more specific visuomotor integration is largely unexplored. We addressed this question by developing robust 3D video reconstruction of mouse head and body during spontaneous exploration paired with simultaneous neuronal recordings from dLGN. Unbiased evaluation of a wide range of postures and movements revealed a widespread coupling between neuronal activity and few behavioral parameters. In particular, postures associated with the animal looking up/down correlated with activity in >50% neurons, and the extent of this effect was comparable with that induced by full-body movements (typically locomotion). By contrast, thalamic activity was minimally correlated with other postures or movements (e.g., left/right head and body torsions). Importantly, up/down postures and full-body movements were largely independent and jointly coupled to neuronal activity. Thus, although most units were excited during full-body movements, some expressed highest firing when the animal was looking up (“look-up” neurons), whereas others expressed highest firing when the animal was looking down (“look-down” neurons). These results were observed in the dark, thus representing a genuine behavioral modulation, and were amplified in a lit arena. Our results demonstrate that the primary visual thalamus, beyond global modulations by sleep/awake states, is potentially involved in specific visuomotor integration and reveal two distinct couplings between up/down postures and neuronal activity.
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spelling pubmed-96167382022-10-31 Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration Orlowska-Feuer, Patrycja Ebrahimi, Aghileh S. Zippo, Antonio G. Petersen, Rasmus S. Lucas, Robert J. Storchi, Riccardo Curr Biol Article Visual information reaches cortex via the thalamic dorsal lateral geniculate nucleus (dLGN). dLGN activity is modulated by global sleep/wake states and arousal, indicating that it is not simply a passive relay station. However, its potential for more specific visuomotor integration is largely unexplored. We addressed this question by developing robust 3D video reconstruction of mouse head and body during spontaneous exploration paired with simultaneous neuronal recordings from dLGN. Unbiased evaluation of a wide range of postures and movements revealed a widespread coupling between neuronal activity and few behavioral parameters. In particular, postures associated with the animal looking up/down correlated with activity in >50% neurons, and the extent of this effect was comparable with that induced by full-body movements (typically locomotion). By contrast, thalamic activity was minimally correlated with other postures or movements (e.g., left/right head and body torsions). Importantly, up/down postures and full-body movements were largely independent and jointly coupled to neuronal activity. Thus, although most units were excited during full-body movements, some expressed highest firing when the animal was looking up (“look-up” neurons), whereas others expressed highest firing when the animal was looking down (“look-down” neurons). These results were observed in the dark, thus representing a genuine behavioral modulation, and were amplified in a lit arena. Our results demonstrate that the primary visual thalamus, beyond global modulations by sleep/awake states, is potentially involved in specific visuomotor integration and reveal two distinct couplings between up/down postures and neuronal activity. Cell Press 2022-09-26 /pmc/articles/PMC9616738/ /pubmed/35973431 http://dx.doi.org/10.1016/j.cub.2022.07.049 Text en © 2022 The Author(s) 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/).
spellingShingle Article
Orlowska-Feuer, Patrycja
Ebrahimi, Aghileh S.
Zippo, Antonio G.
Petersen, Rasmus S.
Lucas, Robert J.
Storchi, Riccardo
Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration
title Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration
title_full Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration
title_fullStr Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration
title_full_unstemmed Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration
title_short Look-up and look-down neurons in the mouse visual thalamus during freely moving exploration
title_sort look-up and look-down neurons in the mouse visual thalamus during freely moving exploration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616738/
https://www.ncbi.nlm.nih.gov/pubmed/35973431
http://dx.doi.org/10.1016/j.cub.2022.07.049
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