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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7521927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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