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...
Autores principales: | , , |
---|---|
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 |