Cargando…
Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning
Cerebellar climbing fibers convey diverse signals, but how they are organized in the compartmental structure of the cerebellar cortex during learning remains largely unclear. We analyzed a large amount of coordinate-localized two-photon imaging data from cerebellar Crus II in mice undergoing ‘Go/No-...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531405/ https://www.ncbi.nlm.nih.gov/pubmed/37712651 http://dx.doi.org/10.7554/eLife.86340 |
_version_ | 1785111710928994304 |
---|---|
author | Hoang, Huu Tsutsumi, Shinichiro Matsuzaki, Masanori Kano, Masanobu Kawato, Mitsuo Kitamura, Kazuo Toyama, Keisuke |
author_facet | Hoang, Huu Tsutsumi, Shinichiro Matsuzaki, Masanori Kano, Masanobu Kawato, Mitsuo Kitamura, Kazuo Toyama, Keisuke |
author_sort | Hoang, Huu |
collection | PubMed |
description | Cerebellar climbing fibers convey diverse signals, but how they are organized in the compartmental structure of the cerebellar cortex during learning remains largely unclear. We analyzed a large amount of coordinate-localized two-photon imaging data from cerebellar Crus II in mice undergoing ‘Go/No-go’ reinforcement learning. Tensor component analysis revealed that a majority of climbing fiber inputs to Purkinje cells were reduced to only four functional components, corresponding to accurate timing control of motor initiation related to a Go cue, cognitive error-based learning, reward processing, and inhibition of erroneous behaviors after a No-go cue. Changes in neural activities during learning of the first two components were correlated with corresponding changes in timing control and error learning across animals, indirectly suggesting causal relationships. Spatial distribution of these components coincided well with boundaries of Aldolase-C/zebrin II expression in Purkinje cells, whereas several components are mixed in single neurons. Synchronization within individual components was bidirectionally regulated according to specific task contexts and learning stages. These findings suggest that, in close collaborations with other brain regions including the inferior olive nucleus, the cerebellum, based on anatomical compartments, reduces dimensions of the learning space by dynamically organizing multiple functional components, a feature that may inspire new-generation AI designs. |
format | Online Article Text |
id | pubmed-10531405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-105314052023-09-28 Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning Hoang, Huu Tsutsumi, Shinichiro Matsuzaki, Masanori Kano, Masanobu Kawato, Mitsuo Kitamura, Kazuo Toyama, Keisuke eLife Computational and Systems Biology Cerebellar climbing fibers convey diverse signals, but how they are organized in the compartmental structure of the cerebellar cortex during learning remains largely unclear. We analyzed a large amount of coordinate-localized two-photon imaging data from cerebellar Crus II in mice undergoing ‘Go/No-go’ reinforcement learning. Tensor component analysis revealed that a majority of climbing fiber inputs to Purkinje cells were reduced to only four functional components, corresponding to accurate timing control of motor initiation related to a Go cue, cognitive error-based learning, reward processing, and inhibition of erroneous behaviors after a No-go cue. Changes in neural activities during learning of the first two components were correlated with corresponding changes in timing control and error learning across animals, indirectly suggesting causal relationships. Spatial distribution of these components coincided well with boundaries of Aldolase-C/zebrin II expression in Purkinje cells, whereas several components are mixed in single neurons. Synchronization within individual components was bidirectionally regulated according to specific task contexts and learning stages. These findings suggest that, in close collaborations with other brain regions including the inferior olive nucleus, the cerebellum, based on anatomical compartments, reduces dimensions of the learning space by dynamically organizing multiple functional components, a feature that may inspire new-generation AI designs. eLife Sciences Publications, Ltd 2023-09-15 /pmc/articles/PMC10531405/ /pubmed/37712651 http://dx.doi.org/10.7554/eLife.86340 Text en © 2023, Hoang, Tsutsumi et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Hoang, Huu Tsutsumi, Shinichiro Matsuzaki, Masanori Kano, Masanobu Kawato, Mitsuo Kitamura, Kazuo Toyama, Keisuke Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning |
title | Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning |
title_full | Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning |
title_fullStr | Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning |
title_full_unstemmed | Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning |
title_short | Dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning |
title_sort | dynamic organization of cerebellar climbing fiber response and synchrony in multiple functional components reduces dimensions for reinforcement learning |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531405/ https://www.ncbi.nlm.nih.gov/pubmed/37712651 http://dx.doi.org/10.7554/eLife.86340 |
work_keys_str_mv | AT hoanghuu dynamicorganizationofcerebellarclimbingfiberresponseandsynchronyinmultiplefunctionalcomponentsreducesdimensionsforreinforcementlearning AT tsutsumishinichiro dynamicorganizationofcerebellarclimbingfiberresponseandsynchronyinmultiplefunctionalcomponentsreducesdimensionsforreinforcementlearning AT matsuzakimasanori dynamicorganizationofcerebellarclimbingfiberresponseandsynchronyinmultiplefunctionalcomponentsreducesdimensionsforreinforcementlearning AT kanomasanobu dynamicorganizationofcerebellarclimbingfiberresponseandsynchronyinmultiplefunctionalcomponentsreducesdimensionsforreinforcementlearning AT kawatomitsuo dynamicorganizationofcerebellarclimbingfiberresponseandsynchronyinmultiplefunctionalcomponentsreducesdimensionsforreinforcementlearning AT kitamurakazuo dynamicorganizationofcerebellarclimbingfiberresponseandsynchronyinmultiplefunctionalcomponentsreducesdimensionsforreinforcementlearning AT toyamakeisuke dynamicorganizationofcerebellarclimbingfiberresponseandsynchronyinmultiplefunctionalcomponentsreducesdimensionsforreinforcementlearning |