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Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus
To produce goal-directed eye movements known as saccades, we must channel sensory input from our environment through a process known as sensorimotor transformation. The behavioral output of this phenomenon (an accurate eye movement) is straightforward, but the coordinated activity of neurons underly...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881850/ https://www.ncbi.nlm.nih.gov/pubmed/36711849 http://dx.doi.org/10.1101/2023.01.03.522634 |
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author | Heusser, Michelle R. Jagadisan, Uday K. Gandhi, Neeraj J. |
author_facet | Heusser, Michelle R. Jagadisan, Uday K. Gandhi, Neeraj J. |
author_sort | Heusser, Michelle R. |
collection | PubMed |
description | To produce goal-directed eye movements known as saccades, we must channel sensory input from our environment through a process known as sensorimotor transformation. The behavioral output of this phenomenon (an accurate eye movement) is straightforward, but the coordinated activity of neurons underlying its dynamics is not well understood. We searched for a neural correlate of sensorimotor transformation in the activity patterns of simultaneously recorded neurons in the superior colliculus (SC) of three male rhesus monkeys performing a visually guided, delayed saccade task. Neurons in the intermediate layers produce a burst of spikes both following the appearance of a visual (sensory) stimulus and preceding an eye movement command, but many also exhibit a sustained activity level during the intervening time (“delay period”). This sustained activity could be representative of visual processing or motor preparation, along with countless cognitive processes. Using a novel measure we call the Visuomotor Proximity Index (VMPI), we pitted visual and motor signals against each other by measuring the degree to which each session’s population activity (as summarized in a low-dimensional framework) could be considered more visual-like or more motor-like. The analysis highlighted two salient features of sensorimotor transformation. One, population activity on average drifted systematically toward a motor-like representation and intermittently reverted to a visual-like representation following a microsaccade. Two, activity patterns that drift to a stronger motor-like representation by the end of the delay period may enable a more rapid initiation of a saccade, substantiating the idea that this movement initiation mechanism is conserved across motor systems. |
format | Online Article Text |
id | pubmed-9881850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-98818502023-01-28 Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus Heusser, Michelle R. Jagadisan, Uday K. Gandhi, Neeraj J. bioRxiv Article To produce goal-directed eye movements known as saccades, we must channel sensory input from our environment through a process known as sensorimotor transformation. The behavioral output of this phenomenon (an accurate eye movement) is straightforward, but the coordinated activity of neurons underlying its dynamics is not well understood. We searched for a neural correlate of sensorimotor transformation in the activity patterns of simultaneously recorded neurons in the superior colliculus (SC) of three male rhesus monkeys performing a visually guided, delayed saccade task. Neurons in the intermediate layers produce a burst of spikes both following the appearance of a visual (sensory) stimulus and preceding an eye movement command, but many also exhibit a sustained activity level during the intervening time (“delay period”). This sustained activity could be representative of visual processing or motor preparation, along with countless cognitive processes. Using a novel measure we call the Visuomotor Proximity Index (VMPI), we pitted visual and motor signals against each other by measuring the degree to which each session’s population activity (as summarized in a low-dimensional framework) could be considered more visual-like or more motor-like. The analysis highlighted two salient features of sensorimotor transformation. One, population activity on average drifted systematically toward a motor-like representation and intermittently reverted to a visual-like representation following a microsaccade. Two, activity patterns that drift to a stronger motor-like representation by the end of the delay period may enable a more rapid initiation of a saccade, substantiating the idea that this movement initiation mechanism is conserved across motor systems. Cold Spring Harbor Laboratory 2023-07-24 /pmc/articles/PMC9881850/ /pubmed/36711849 http://dx.doi.org/10.1101/2023.01.03.522634 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Heusser, Michelle R. Jagadisan, Uday K. Gandhi, Neeraj J. Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus |
title | Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus |
title_full | Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus |
title_fullStr | Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus |
title_full_unstemmed | Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus |
title_short | Drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus |
title_sort | drifting population dynamics with transient resets characterize sensorimotor transformation in the monkey superior colliculus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881850/ https://www.ncbi.nlm.nih.gov/pubmed/36711849 http://dx.doi.org/10.1101/2023.01.03.522634 |
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