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Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity
The rate and temporal pattern of neural spiking each have the potential to influence computation. In the cerebellum, it has been hypothesized that the irregularity of interspike intervals in Purkinje cells affects their ability to transmit information to downstream neurons. Accordingly, during oculo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499540/ https://www.ncbi.nlm.nih.gov/pubmed/31050648 http://dx.doi.org/10.7554/eLife.37102 |
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author | Payne, Hannah L French, Ranran L Guo, Christine C Nguyen-Vu, TD Barbara Manninen, Tiina Raymond, Jennifer L |
author_facet | Payne, Hannah L French, Ranran L Guo, Christine C Nguyen-Vu, TD Barbara Manninen, Tiina Raymond, Jennifer L |
author_sort | Payne, Hannah L |
collection | PubMed |
description | The rate and temporal pattern of neural spiking each have the potential to influence computation. In the cerebellum, it has been hypothesized that the irregularity of interspike intervals in Purkinje cells affects their ability to transmit information to downstream neurons. Accordingly, during oculomotor behavior in mice and rhesus monkeys, mean irregularity of Purkinje cell spiking varied with mean eye velocity. However, moment-to-moment variations revealed a tight correlation between eye velocity and spike rate, with no additional information conveyed by spike irregularity. Moreover, when spike rate and irregularity were independently controlled using optogenetic stimulation, the eye movements elicited were well-described by a linear population rate code with 3–5 ms temporal precision. Biophysical and random-walk models identified biologically realistic parameter ranges that determine whether spike irregularity influences responses downstream. The results demonstrate cerebellar control of movements through a remarkably rapid rate code, with no evidence for an additional contribution of spike irregularity. |
format | Online Article Text |
id | pubmed-6499540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-64995402019-05-06 Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity Payne, Hannah L French, Ranran L Guo, Christine C Nguyen-Vu, TD Barbara Manninen, Tiina Raymond, Jennifer L eLife Neuroscience The rate and temporal pattern of neural spiking each have the potential to influence computation. In the cerebellum, it has been hypothesized that the irregularity of interspike intervals in Purkinje cells affects their ability to transmit information to downstream neurons. Accordingly, during oculomotor behavior in mice and rhesus monkeys, mean irregularity of Purkinje cell spiking varied with mean eye velocity. However, moment-to-moment variations revealed a tight correlation between eye velocity and spike rate, with no additional information conveyed by spike irregularity. Moreover, when spike rate and irregularity were independently controlled using optogenetic stimulation, the eye movements elicited were well-described by a linear population rate code with 3–5 ms temporal precision. Biophysical and random-walk models identified biologically realistic parameter ranges that determine whether spike irregularity influences responses downstream. The results demonstrate cerebellar control of movements through a remarkably rapid rate code, with no evidence for an additional contribution of spike irregularity. eLife Sciences Publications, Ltd 2019-05-03 /pmc/articles/PMC6499540/ /pubmed/31050648 http://dx.doi.org/10.7554/eLife.37102 Text en © 2019, Payne 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 Payne, Hannah L French, Ranran L Guo, Christine C Nguyen-Vu, TD Barbara Manninen, Tiina Raymond, Jennifer L Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity |
title | Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity |
title_full | Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity |
title_fullStr | Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity |
title_full_unstemmed | Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity |
title_short | Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity |
title_sort | cerebellar purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499540/ https://www.ncbi.nlm.nih.gov/pubmed/31050648 http://dx.doi.org/10.7554/eLife.37102 |
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