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Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice

Animals investigate their environments by directing their gaze towards salient stimuli. In the prevailing view, mouse gaze shifts entail head rotations followed by brainstem-mediated eye movements, including saccades to reset the eyes. These ‘recentering’ saccades are attributed to head movement-rel...

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Autores principales: Zahler, Sebastian H, Taylor, David E, Wong, Joey Y, Adams, Julia M, Feinberg, Evan H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747496/
https://www.ncbi.nlm.nih.gov/pubmed/34970968
http://dx.doi.org/10.7554/eLife.73081
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author Zahler, Sebastian H
Taylor, David E
Wong, Joey Y
Adams, Julia M
Feinberg, Evan H
author_facet Zahler, Sebastian H
Taylor, David E
Wong, Joey Y
Adams, Julia M
Feinberg, Evan H
author_sort Zahler, Sebastian H
collection PubMed
description Animals investigate their environments by directing their gaze towards salient stimuli. In the prevailing view, mouse gaze shifts entail head rotations followed by brainstem-mediated eye movements, including saccades to reset the eyes. These ‘recentering’ saccades are attributed to head movement-related vestibular cues. However, microstimulating mouse superior colliculus (SC) elicits directed head and eye movements resembling SC-dependent sensory-guided gaze shifts in other species, suggesting that mouse gaze shifts may be more flexible than has been recognized. We investigated this possibility by tracking eye and attempted head movements in a head-fixed preparation that eliminates head movement-related sensory cues. We found tactile stimuli evoke directionally biased saccades coincident with attempted head rotations. Differences in saccade endpoints across stimuli are associated with distinct stimulus-dependent relationships between initial eye position and saccade direction and amplitude. Optogenetic perturbations revealed SC drives these gaze shifts. Thus, head-fixed mice make sensory-guided, SC-dependent gaze shifts involving coincident, directionally biased saccades and attempted head movements. Our findings uncover flexibility in mouse gaze shifts and provide a foundation for studying head-eye coupling.
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spelling pubmed-87474962022-01-12 Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice Zahler, Sebastian H Taylor, David E Wong, Joey Y Adams, Julia M Feinberg, Evan H eLife Neuroscience Animals investigate their environments by directing their gaze towards salient stimuli. In the prevailing view, mouse gaze shifts entail head rotations followed by brainstem-mediated eye movements, including saccades to reset the eyes. These ‘recentering’ saccades are attributed to head movement-related vestibular cues. However, microstimulating mouse superior colliculus (SC) elicits directed head and eye movements resembling SC-dependent sensory-guided gaze shifts in other species, suggesting that mouse gaze shifts may be more flexible than has been recognized. We investigated this possibility by tracking eye and attempted head movements in a head-fixed preparation that eliminates head movement-related sensory cues. We found tactile stimuli evoke directionally biased saccades coincident with attempted head rotations. Differences in saccade endpoints across stimuli are associated with distinct stimulus-dependent relationships between initial eye position and saccade direction and amplitude. Optogenetic perturbations revealed SC drives these gaze shifts. Thus, head-fixed mice make sensory-guided, SC-dependent gaze shifts involving coincident, directionally biased saccades and attempted head movements. Our findings uncover flexibility in mouse gaze shifts and provide a foundation for studying head-eye coupling. eLife Sciences Publications, Ltd 2021-12-31 /pmc/articles/PMC8747496/ /pubmed/34970968 http://dx.doi.org/10.7554/eLife.73081 Text en © 2021, Zahler 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
Zahler, Sebastian H
Taylor, David E
Wong, Joey Y
Adams, Julia M
Feinberg, Evan H
Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice
title Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice
title_full Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice
title_fullStr Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice
title_full_unstemmed Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice
title_short Superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice
title_sort superior colliculus drives stimulus-evoked directionally biased saccades and attempted head movements in head-fixed mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747496/
https://www.ncbi.nlm.nih.gov/pubmed/34970968
http://dx.doi.org/10.7554/eLife.73081
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