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Model cerebellar granule cells can faithfully transmit modulated firing rate signals
A crucial assumption of many high-level system models of the cerebellum is that information in the granular layer is encoded in a linear manner. However, granule cells are known for their non-linear and resonant synaptic and intrinsic properties that could potentially impede linear signal transmissi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195316/ https://www.ncbi.nlm.nih.gov/pubmed/25352777 http://dx.doi.org/10.3389/fncel.2014.00304 |
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author | Rössert, Christian Solinas, Sergio D'Angelo, Egidio Dean, Paul Porrill, John |
author_facet | Rössert, Christian Solinas, Sergio D'Angelo, Egidio Dean, Paul Porrill, John |
author_sort | Rössert, Christian |
collection | PubMed |
description | A crucial assumption of many high-level system models of the cerebellum is that information in the granular layer is encoded in a linear manner. However, granule cells are known for their non-linear and resonant synaptic and intrinsic properties that could potentially impede linear signal transmission. In this modeling study we analyse how electrophysiological granule cell properties and spike sampling influence information coded by firing rate modulation, assuming no signal-related, i.e., uncorrelated inhibitory feedback (open-loop mode). A detailed one-compartment granule cell model was excited in simulation by either direct current or mossy-fiber synaptic inputs. Vestibular signals were represented as tonic inputs to the flocculus modulated at frequencies up to 20 Hz (approximate upper frequency limit of vestibular-ocular reflex, VOR). Model outputs were assessed using estimates of both the transfer function, and the fidelity of input-signal reconstruction measured as variance-accounted-for. The detailed granule cell model with realistic mossy-fiber synaptic inputs could transmit information faithfully and linearly in the frequency range of the vestibular-ocular reflex. This was achieved most simply if the model neurons had a firing rate at least twice the highest required frequency of modulation, but lower rates were also adequate provided a population of neurons was utilized, especially in combination with push-pull coding. The exact number of neurons required for faithful transmission depended on the precise values of firing rate and noise. The model neurons were also able to combine excitatory and inhibitory signals linearly, and could be replaced by a simpler (modified) integrate-and-fire neuron in the case of high tonic firing rates. These findings suggest that granule cells can in principle code modulated firing-rate inputs in a linear manner, and are thus consistent with the high-level adaptive-filter model of the cerebellar microcircuit. |
format | Online Article Text |
id | pubmed-4195316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41953162014-10-28 Model cerebellar granule cells can faithfully transmit modulated firing rate signals Rössert, Christian Solinas, Sergio D'Angelo, Egidio Dean, Paul Porrill, John Front Cell Neurosci Neuroscience A crucial assumption of many high-level system models of the cerebellum is that information in the granular layer is encoded in a linear manner. However, granule cells are known for their non-linear and resonant synaptic and intrinsic properties that could potentially impede linear signal transmission. In this modeling study we analyse how electrophysiological granule cell properties and spike sampling influence information coded by firing rate modulation, assuming no signal-related, i.e., uncorrelated inhibitory feedback (open-loop mode). A detailed one-compartment granule cell model was excited in simulation by either direct current or mossy-fiber synaptic inputs. Vestibular signals were represented as tonic inputs to the flocculus modulated at frequencies up to 20 Hz (approximate upper frequency limit of vestibular-ocular reflex, VOR). Model outputs were assessed using estimates of both the transfer function, and the fidelity of input-signal reconstruction measured as variance-accounted-for. The detailed granule cell model with realistic mossy-fiber synaptic inputs could transmit information faithfully and linearly in the frequency range of the vestibular-ocular reflex. This was achieved most simply if the model neurons had a firing rate at least twice the highest required frequency of modulation, but lower rates were also adequate provided a population of neurons was utilized, especially in combination with push-pull coding. The exact number of neurons required for faithful transmission depended on the precise values of firing rate and noise. The model neurons were also able to combine excitatory and inhibitory signals linearly, and could be replaced by a simpler (modified) integrate-and-fire neuron in the case of high tonic firing rates. These findings suggest that granule cells can in principle code modulated firing-rate inputs in a linear manner, and are thus consistent with the high-level adaptive-filter model of the cerebellar microcircuit. Frontiers Media S.A. 2014-10-13 /pmc/articles/PMC4195316/ /pubmed/25352777 http://dx.doi.org/10.3389/fncel.2014.00304 Text en Copyright © 2014 Rössert, Solinas, D'Angelo, Dean and Porrill. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Rössert, Christian Solinas, Sergio D'Angelo, Egidio Dean, Paul Porrill, John Model cerebellar granule cells can faithfully transmit modulated firing rate signals |
title | Model cerebellar granule cells can faithfully transmit modulated firing rate signals |
title_full | Model cerebellar granule cells can faithfully transmit modulated firing rate signals |
title_fullStr | Model cerebellar granule cells can faithfully transmit modulated firing rate signals |
title_full_unstemmed | Model cerebellar granule cells can faithfully transmit modulated firing rate signals |
title_short | Model cerebellar granule cells can faithfully transmit modulated firing rate signals |
title_sort | model cerebellar granule cells can faithfully transmit modulated firing rate signals |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195316/ https://www.ncbi.nlm.nih.gov/pubmed/25352777 http://dx.doi.org/10.3389/fncel.2014.00304 |
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