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Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells
The cerebellar cortex performs computations that are critical for control of our actions, and then transmits that information via simple spikes of Purkinje cells (P-cells) to downstream structures. However, because P-cells are many synapses away from muscles, we do not know how their output affects...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120735/ https://www.ncbi.nlm.nih.gov/pubmed/37090615 http://dx.doi.org/10.1101/2023.04.16.537034 |
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author | Muller, Salomon Z. Pi, Jay S. Hage, Paul Fakharian, Mohammad Amin Sedaghat-Nejad, Ehsan Shadmehr, Reza |
author_facet | Muller, Salomon Z. Pi, Jay S. Hage, Paul Fakharian, Mohammad Amin Sedaghat-Nejad, Ehsan Shadmehr, Reza |
author_sort | Muller, Salomon Z. |
collection | PubMed |
description | The cerebellar cortex performs computations that are critical for control of our actions, and then transmits that information via simple spikes of Purkinje cells (P-cells) to downstream structures. However, because P-cells are many synapses away from muscles, we do not know how their output affects behavior. Furthermore, we do not know the level of abstraction, i.e., the coordinate system of the P-cell’s output. Here, we recorded spiking activities of hundreds of P-cells in the oculomotor vermis of marmosets during saccadic eye movements and found that following the presentation of a visual stimulus, the olivary input to a P-cell encoded a probabilistic signal that coarsely described both the direction and the amplitude of that stimulus. When this input was present, the resulting complex spike briefly suppressed the P-cell’s simple spikes, disrupting the P-cell’s output during that saccade. Remarkably, this brief suppression altered the saccade’s trajectory by pulling the eyes toward the part of the visual space that was preferentially encoded by the olivary input to that P-cell. Thus, analysis of behavior in the milliseconds following a complex spike unmasked how the P-cell’s output influenced behavior: the preferred location in the coordinates of the visual system as conveyed probabilistically from the inferior olive to a P-cell defined the action in the coordinates of the motor system for which that P-cell’s simple spikes directed behavior. |
format | Online Article Text |
id | pubmed-10120735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101207352023-04-22 Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells Muller, Salomon Z. Pi, Jay S. Hage, Paul Fakharian, Mohammad Amin Sedaghat-Nejad, Ehsan Shadmehr, Reza bioRxiv Article The cerebellar cortex performs computations that are critical for control of our actions, and then transmits that information via simple spikes of Purkinje cells (P-cells) to downstream structures. However, because P-cells are many synapses away from muscles, we do not know how their output affects behavior. Furthermore, we do not know the level of abstraction, i.e., the coordinate system of the P-cell’s output. Here, we recorded spiking activities of hundreds of P-cells in the oculomotor vermis of marmosets during saccadic eye movements and found that following the presentation of a visual stimulus, the olivary input to a P-cell encoded a probabilistic signal that coarsely described both the direction and the amplitude of that stimulus. When this input was present, the resulting complex spike briefly suppressed the P-cell’s simple spikes, disrupting the P-cell’s output during that saccade. Remarkably, this brief suppression altered the saccade’s trajectory by pulling the eyes toward the part of the visual space that was preferentially encoded by the olivary input to that P-cell. Thus, analysis of behavior in the milliseconds following a complex spike unmasked how the P-cell’s output influenced behavior: the preferred location in the coordinates of the visual system as conveyed probabilistically from the inferior olive to a P-cell defined the action in the coordinates of the motor system for which that P-cell’s simple spikes directed behavior. Cold Spring Harbor Laboratory 2023-04-16 /pmc/articles/PMC10120735/ /pubmed/37090615 http://dx.doi.org/10.1101/2023.04.16.537034 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 Muller, Salomon Z. Pi, Jay S. Hage, Paul Fakharian, Mohammad Amin Sedaghat-Nejad, Ehsan Shadmehr, Reza Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells |
title | Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells |
title_full | Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells |
title_fullStr | Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells |
title_full_unstemmed | Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells |
title_short | Complex spikes perturb movements, revealing the sensorimotor map of Purkinje cells |
title_sort | complex spikes perturb movements, revealing the sensorimotor map of purkinje cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120735/ https://www.ncbi.nlm.nih.gov/pubmed/37090615 http://dx.doi.org/10.1101/2023.04.16.537034 |
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