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Neural variability determines coding strategies for natural self-motion in macaque monkeys

We have previously reported that central neurons mediating vestibulo-spinal reflexes and self-motion perception optimally encode natural self-motion (Mitchell et al., 2018). Importantly however, the vestibular nuclei also comprise other neuronal classes that mediate essential functions such as the v...

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Autores principales: Mackrous, Isabelle, Carriot, Jérome, Cullen, Kathleen E, Chacron, Maurice J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521927/
https://www.ncbi.nlm.nih.gov/pubmed/32915134
http://dx.doi.org/10.7554/eLife.57484
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author Mackrous, Isabelle
Carriot, Jérome
Cullen, Kathleen E
Chacron, Maurice J
author_facet Mackrous, Isabelle
Carriot, Jérome
Cullen, Kathleen E
Chacron, Maurice J
author_sort Mackrous, Isabelle
collection PubMed
description We have previously reported that central neurons mediating vestibulo-spinal reflexes and self-motion perception optimally encode natural self-motion (Mitchell et al., 2018). Importantly however, the vestibular nuclei also comprise other neuronal classes that mediate essential functions such as the vestibulo-ocular reflex (VOR) and its adaptation. Here we show that heterogeneities in resting discharge variability mediate a trade-off between faithful encoding and optimal coding via temporal whitening. Specifically, neurons displaying lower variability did not whiten naturalistic self-motion but instead faithfully represented the stimulus’ detailed time course, while neurons displaying higher variability displayed temporal whitening. Using a well-established model of VOR pathways, we demonstrate that faithful stimulus encoding is necessary to generate the compensatory eye movements found experimentally during naturalistic self-motion. Our findings suggest a novel functional role for variability toward establishing different coding strategies: (1) faithful stimulus encoding for generating the VOR; (2) optimized coding via temporal whitening for other vestibular functions.
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spelling pubmed-75219272020-09-30 Neural variability determines coding strategies for natural self-motion in macaque monkeys Mackrous, Isabelle Carriot, Jérome Cullen, Kathleen E Chacron, Maurice J eLife Neuroscience We have previously reported that central neurons mediating vestibulo-spinal reflexes and self-motion perception optimally encode natural self-motion (Mitchell et al., 2018). Importantly however, the vestibular nuclei also comprise other neuronal classes that mediate essential functions such as the vestibulo-ocular reflex (VOR) and its adaptation. Here we show that heterogeneities in resting discharge variability mediate a trade-off between faithful encoding and optimal coding via temporal whitening. Specifically, neurons displaying lower variability did not whiten naturalistic self-motion but instead faithfully represented the stimulus’ detailed time course, while neurons displaying higher variability displayed temporal whitening. Using a well-established model of VOR pathways, we demonstrate that faithful stimulus encoding is necessary to generate the compensatory eye movements found experimentally during naturalistic self-motion. Our findings suggest a novel functional role for variability toward establishing different coding strategies: (1) faithful stimulus encoding for generating the VOR; (2) optimized coding via temporal whitening for other vestibular functions. eLife Sciences Publications, Ltd 2020-09-11 /pmc/articles/PMC7521927/ /pubmed/32915134 http://dx.doi.org/10.7554/eLife.57484 Text en © 2020, Mackrous et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Mackrous, Isabelle
Carriot, Jérome
Cullen, Kathleen E
Chacron, Maurice J
Neural variability determines coding strategies for natural self-motion in macaque monkeys
title Neural variability determines coding strategies for natural self-motion in macaque monkeys
title_full Neural variability determines coding strategies for natural self-motion in macaque monkeys
title_fullStr Neural variability determines coding strategies for natural self-motion in macaque monkeys
title_full_unstemmed Neural variability determines coding strategies for natural self-motion in macaque monkeys
title_short Neural variability determines coding strategies for natural self-motion in macaque monkeys
title_sort neural variability determines coding strategies for natural self-motion in macaque monkeys
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521927/
https://www.ncbi.nlm.nih.gov/pubmed/32915134
http://dx.doi.org/10.7554/eLife.57484
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