Cargando…

Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts

Gaze saccades, rapid shifts of the eyes and head toward a goal, have provided fundamental insights into the neural control of movement. For example, it has been shown that the superior colliculus (SC) transforms a visual target (T) code to future gaze (G) location commands after a memory delay. Howe...

Descripción completa

Detalles Bibliográficos
Autores principales: Sadeh, Morteza, Sajad, Amirsaman, Wang, Hongying, Yan, Xiaogang, Crawford, John Douglas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944480/
https://www.ncbi.nlm.nih.gov/pubmed/31792117
http://dx.doi.org/10.1523/ENEURO.0359-18.2019
_version_ 1783485038043594752
author Sadeh, Morteza
Sajad, Amirsaman
Wang, Hongying
Yan, Xiaogang
Crawford, John Douglas
author_facet Sadeh, Morteza
Sajad, Amirsaman
Wang, Hongying
Yan, Xiaogang
Crawford, John Douglas
author_sort Sadeh, Morteza
collection PubMed
description Gaze saccades, rapid shifts of the eyes and head toward a goal, have provided fundamental insights into the neural control of movement. For example, it has been shown that the superior colliculus (SC) transforms a visual target (T) code to future gaze (G) location commands after a memory delay. However, this transformation has not been observed in “reactive” saccades made directly to a stimulus, so its contribution to normal gaze behavior is unclear. Here, we tested this using a quantitative measure of the intermediate codes between T and G, based on variable errors in gaze endpoints. We demonstrate that a rapid spatial transformation occurs within the primate’s SC (Macaca mulatta) during reactive saccades, involving a shift in coding from T, through intermediate codes, to G. This spatial shift progressed continuously both across and within cell populations [visual, visuomotor (VM), motor], rather than relaying discretely between populations with fixed spatial codes. These results suggest that the SC produces a rapid, noisy, and distributed transformation that contributes to variable errors in reactive gaze shifts.
format Online
Article
Text
id pubmed-6944480
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-69444802020-01-07 Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts Sadeh, Morteza Sajad, Amirsaman Wang, Hongying Yan, Xiaogang Crawford, John Douglas eNeuro New Research Gaze saccades, rapid shifts of the eyes and head toward a goal, have provided fundamental insights into the neural control of movement. For example, it has been shown that the superior colliculus (SC) transforms a visual target (T) code to future gaze (G) location commands after a memory delay. However, this transformation has not been observed in “reactive” saccades made directly to a stimulus, so its contribution to normal gaze behavior is unclear. Here, we tested this using a quantitative measure of the intermediate codes between T and G, based on variable errors in gaze endpoints. We demonstrate that a rapid spatial transformation occurs within the primate’s SC (Macaca mulatta) during reactive saccades, involving a shift in coding from T, through intermediate codes, to G. This spatial shift progressed continuously both across and within cell populations [visual, visuomotor (VM), motor], rather than relaying discretely between populations with fixed spatial codes. These results suggest that the SC produces a rapid, noisy, and distributed transformation that contributes to variable errors in reactive gaze shifts. Society for Neuroscience 2020-01-02 /pmc/articles/PMC6944480/ /pubmed/31792117 http://dx.doi.org/10.1523/ENEURO.0359-18.2019 Text en Copyright © 2020 Sadeh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Sadeh, Morteza
Sajad, Amirsaman
Wang, Hongying
Yan, Xiaogang
Crawford, John Douglas
Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts
title Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts
title_full Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts
title_fullStr Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts
title_full_unstemmed Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts
title_short Timing Determines Tuning: A Rapid Spatial Transformation in Superior Colliculus Neurons during Reactive Gaze Shifts
title_sort timing determines tuning: a rapid spatial transformation in superior colliculus neurons during reactive gaze shifts
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944480/
https://www.ncbi.nlm.nih.gov/pubmed/31792117
http://dx.doi.org/10.1523/ENEURO.0359-18.2019
work_keys_str_mv AT sadehmorteza timingdeterminestuningarapidspatialtransformationinsuperiorcolliculusneuronsduringreactivegazeshifts
AT sajadamirsaman timingdeterminestuningarapidspatialtransformationinsuperiorcolliculusneuronsduringreactivegazeshifts
AT wanghongying timingdeterminestuningarapidspatialtransformationinsuperiorcolliculusneuronsduringreactivegazeshifts
AT yanxiaogang timingdeterminestuningarapidspatialtransformationinsuperiorcolliculusneuronsduringreactivegazeshifts
AT crawfordjohndouglas timingdeterminestuningarapidspatialtransformationinsuperiorcolliculusneuronsduringreactivegazeshifts