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Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs
Without synaptic input, Purkinje neurons can spontaneously fire in a repeating trimodal pattern that consists of tonic spiking, bursting and quiescence. Climbing fiber input (CF) switches Purkinje neurons out of the trimodal firing pattern and toggles them between a tonic firing and a quiescent stat...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138505/ https://www.ncbi.nlm.nih.gov/pubmed/25191262 http://dx.doi.org/10.3389/fncom.2014.00086 |
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author | Forrest, Michael D. |
author_facet | Forrest, Michael D. |
author_sort | Forrest, Michael D. |
collection | PubMed |
description | Without synaptic input, Purkinje neurons can spontaneously fire in a repeating trimodal pattern that consists of tonic spiking, bursting and quiescence. Climbing fiber input (CF) switches Purkinje neurons out of the trimodal firing pattern and toggles them between a tonic firing and a quiescent state, while setting the gain of their response to Parallel Fiber (PF) input. The basis to this transition is unclear. We investigate it using a biophysical Purkinje cell model under conditions of CF and PF input. The model can replicate these toggle and gain functions, dependent upon a novel account of intracellular calcium dynamics that we hypothesize to be applicable in real Purkinje cells. |
format | Online Article Text |
id | pubmed-4138505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41385052014-09-04 Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs Forrest, Michael D. Front Comput Neurosci Neuroscience Without synaptic input, Purkinje neurons can spontaneously fire in a repeating trimodal pattern that consists of tonic spiking, bursting and quiescence. Climbing fiber input (CF) switches Purkinje neurons out of the trimodal firing pattern and toggles them between a tonic firing and a quiescent state, while setting the gain of their response to Parallel Fiber (PF) input. The basis to this transition is unclear. We investigate it using a biophysical Purkinje cell model under conditions of CF and PF input. The model can replicate these toggle and gain functions, dependent upon a novel account of intracellular calcium dynamics that we hypothesize to be applicable in real Purkinje cells. Frontiers Media S.A. 2014-08-20 /pmc/articles/PMC4138505/ /pubmed/25191262 http://dx.doi.org/10.3389/fncom.2014.00086 Text en Copyright © 2014 Forrest. http://creativecommons.org/licenses/by/3.0/ 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 Forrest, Michael D. Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs |
title | Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs |
title_full | Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs |
title_fullStr | Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs |
title_full_unstemmed | Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs |
title_short | Intracellular calcium dynamics permit a Purkinje neuron model to perform toggle and gain computations upon its inputs |
title_sort | intracellular calcium dynamics permit a purkinje neuron model to perform toggle and gain computations upon its inputs |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138505/ https://www.ncbi.nlm.nih.gov/pubmed/25191262 http://dx.doi.org/10.3389/fncom.2014.00086 |
work_keys_str_mv | AT forrestmichaeld intracellularcalciumdynamicspermitapurkinjeneuronmodeltoperformtoggleandgaincomputationsuponitsinputs |