Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Majoral, Daniel, Zemmar, Ajmal, Vicente, Raul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034954/
https://www.ncbi.nlm.nih.gov/pubmed/32040505
http://dx.doi.org/10.1371/journal.pcbi.1007601
_version_ 1783499974085967872
author Majoral, Daniel
Zemmar, Ajmal
Vicente, Raul
author_facet Majoral, Daniel
Zemmar, Ajmal
Vicente, Raul
author_sort Majoral, Daniel
collection PubMed
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.
format Online
Article
Text
id pubmed-7034954
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-70349542020-02-28 A model for time interval learning in the Purkinje cell Majoral, Daniel Zemmar, Ajmal Vicente, Raul PLoS Comput Biol Research Article 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. Public Library of Science 2020-02-10 /pmc/articles/PMC7034954/ /pubmed/32040505 http://dx.doi.org/10.1371/journal.pcbi.1007601 Text en © 2020 Majoral et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Majoral, Daniel
Zemmar, Ajmal
Vicente, Raul
A model for time interval learning in the Purkinje cell
title 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_short A model for time interval learning in the Purkinje cell
title_sort model for time interval learning in the purkinje cell
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034954/
https://www.ncbi.nlm.nih.gov/pubmed/32040505
http://dx.doi.org/10.1371/journal.pcbi.1007601
work_keys_str_mv AT majoraldaniel amodelfortimeintervallearninginthepurkinjecell
AT zemmarajmal amodelfortimeintervallearninginthepurkinjecell
AT vicenteraul amodelfortimeintervallearninginthepurkinjecell
AT majoraldaniel modelfortimeintervallearninginthepurkinjecell
AT zemmarajmal modelfortimeintervallearninginthepurkinjecell
AT vicenteraul modelfortimeintervallearninginthepurkinjecell