A model for time interval learning in the Purkinje cell.

Recent experimental findings indicate that Purkinje cells in the cerebellum represent time intervals by mechanisms other than conventional synaptic weights. These findings add to the theoretical and experimental observations suggesting the presence of intra-cellular mechanisms for adaptation and pro...

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Main Authors: Daniel Majoral, Ajmal Zemmar, Raul Vicente
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-02-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1007601
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spelling doaj-3144ce359d504c5a9291223c124058722021-04-21T15:14:05ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582020-02-01162e100760110.1371/journal.pcbi.1007601A model for time interval learning in the Purkinje cell.Daniel MajoralAjmal ZemmarRaul VicenteRecent experimental findings indicate that Purkinje cells in the cerebellum represent time intervals by mechanisms other than conventional synaptic weights. These findings add to the theoretical and experimental observations suggesting the presence of intra-cellular mechanisms for adaptation and processing. To account for these experimental results we propose a new biophysical model for time interval learning in a Purkinje cell. The numerical model focuses on a classical delay conditioning task (e.g. eyeblink conditioning) and relies on a few computational steps. In particular, the model posits the activation by the parallel fiber input of a local intra-cellular calcium store which can be modulated by intra-cellular pathways. The reciprocal interaction of the calcium signal with several proteins forming negative and positive feedback loops ensures that the timing of inhibition in the Purkinje cell anticipates the interval between parallel and climbing fiber inputs during training. We systematically test the model ability to learn time intervals at the 150-1000 ms time scale, while observing that learning can also extend to the multiple seconds scale. In agreement with experimental observations we also show that the number of pairings required to learn increases with inter-stimulus interval. Finally, we discuss how this model would allow the cerebellum to detect and generate specific spatio-temporal patterns, a classical theory for cerebellar function.https://doi.org/10.1371/journal.pcbi.1007601
collection DOAJ
language English
format Article
sources DOAJ
author Daniel Majoral
Ajmal Zemmar
Raul Vicente
spellingShingle Daniel Majoral
Ajmal Zemmar
Raul Vicente
A model for time interval learning in the Purkinje cell.
PLoS Computational Biology
author_facet Daniel Majoral
Ajmal Zemmar
Raul Vicente
author_sort Daniel Majoral
title A model for time interval learning in the Purkinje cell.
title_short A model for time interval learning in the Purkinje cell.
title_full A model for time interval learning in the Purkinje cell.
title_fullStr A model for time interval learning in the Purkinje cell.
title_full_unstemmed A model for time interval learning in the Purkinje cell.
title_sort model for time interval learning in the purkinje cell.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2020-02-01
description Recent experimental findings indicate that Purkinje cells in the cerebellum represent time intervals by mechanisms other than conventional synaptic weights. These findings add to the theoretical and experimental observations suggesting the presence of intra-cellular mechanisms for adaptation and processing. To account for these experimental results we propose a new biophysical model for time interval learning in a Purkinje cell. The numerical model focuses on a classical delay conditioning task (e.g. eyeblink conditioning) and relies on a few computational steps. In particular, the model posits the activation by the parallel fiber input of a local intra-cellular calcium store which can be modulated by intra-cellular pathways. The reciprocal interaction of the calcium signal with several proteins forming negative and positive feedback loops ensures that the timing of inhibition in the Purkinje cell anticipates the interval between parallel and climbing fiber inputs during training. We systematically test the model ability to learn time intervals at the 150-1000 ms time scale, while observing that learning can also extend to the multiple seconds scale. In agreement with experimental observations we also show that the number of pairings required to learn increases with inter-stimulus interval. Finally, we discuss how this model would allow the cerebellum to detect and generate specific spatio-temporal patterns, a classical theory for cerebellar function.
url https://doi.org/10.1371/journal.pcbi.1007601
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