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Synaptic mechanisms for associative learning in the cerebellar nuclei

Associative learning during delay eyeblink conditioning (EBC) depends on an intact cerebellum. However, the relative contribution of changes in the cerebellar nuclei to learning remains a subject of ongoing debate. In particular, little is known about the changes in synaptic inputs to cerebellar nuc...

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Autores principales: Broersen, Robin, Albergaria, Catarina, Carulli, Daniela, Carey, Megan R., Canto, Cathrin B., De Zeeuw, Chris I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662440/
https://www.ncbi.nlm.nih.gov/pubmed/37985778
http://dx.doi.org/10.1038/s41467-023-43227-w
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author Broersen, Robin
Albergaria, Catarina
Carulli, Daniela
Carey, Megan R.
Canto, Cathrin B.
De Zeeuw, Chris I.
author_facet Broersen, Robin
Albergaria, Catarina
Carulli, Daniela
Carey, Megan R.
Canto, Cathrin B.
De Zeeuw, Chris I.
author_sort Broersen, Robin
collection PubMed
description Associative learning during delay eyeblink conditioning (EBC) depends on an intact cerebellum. However, the relative contribution of changes in the cerebellar nuclei to learning remains a subject of ongoing debate. In particular, little is known about the changes in synaptic inputs to cerebellar nuclei neurons that take place during EBC and how they shape the membrane potential of these neurons. Here, we probed the ability of these inputs to support associative learning in mice, and investigated structural and cell-physiological changes within the cerebellar nuclei during learning. We find that optogenetic stimulation of mossy fiber afferents to the anterior interposed nucleus (AIP) can substitute for a conditioned stimulus and is sufficient to elicit conditioned responses (CRs) that are adaptively well-timed. Further, EBC induces structural changes in mossy fiber and inhibitory inputs, but not in climbing fiber inputs, and it leads to changes in subthreshold processing of AIP neurons that correlate with conditioned eyelid movements. The changes in synaptic and spiking activity that precede the CRs allow for a decoder to distinguish trials with a CR. Our data reveal how structural and physiological modifications of synaptic inputs to cerebellar nuclei neurons can facilitate learning.
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spelling pubmed-106624402023-11-20 Synaptic mechanisms for associative learning in the cerebellar nuclei Broersen, Robin Albergaria, Catarina Carulli, Daniela Carey, Megan R. Canto, Cathrin B. De Zeeuw, Chris I. Nat Commun Article Associative learning during delay eyeblink conditioning (EBC) depends on an intact cerebellum. However, the relative contribution of changes in the cerebellar nuclei to learning remains a subject of ongoing debate. In particular, little is known about the changes in synaptic inputs to cerebellar nuclei neurons that take place during EBC and how they shape the membrane potential of these neurons. Here, we probed the ability of these inputs to support associative learning in mice, and investigated structural and cell-physiological changes within the cerebellar nuclei during learning. We find that optogenetic stimulation of mossy fiber afferents to the anterior interposed nucleus (AIP) can substitute for a conditioned stimulus and is sufficient to elicit conditioned responses (CRs) that are adaptively well-timed. Further, EBC induces structural changes in mossy fiber and inhibitory inputs, but not in climbing fiber inputs, and it leads to changes in subthreshold processing of AIP neurons that correlate with conditioned eyelid movements. The changes in synaptic and spiking activity that precede the CRs allow for a decoder to distinguish trials with a CR. Our data reveal how structural and physiological modifications of synaptic inputs to cerebellar nuclei neurons can facilitate learning. Nature Publishing Group UK 2023-11-20 /pmc/articles/PMC10662440/ /pubmed/37985778 http://dx.doi.org/10.1038/s41467-023-43227-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Broersen, Robin
Albergaria, Catarina
Carulli, Daniela
Carey, Megan R.
Canto, Cathrin B.
De Zeeuw, Chris I.
Synaptic mechanisms for associative learning in the cerebellar nuclei
title Synaptic mechanisms for associative learning in the cerebellar nuclei
title_full Synaptic mechanisms for associative learning in the cerebellar nuclei
title_fullStr Synaptic mechanisms for associative learning in the cerebellar nuclei
title_full_unstemmed Synaptic mechanisms for associative learning in the cerebellar nuclei
title_short Synaptic mechanisms for associative learning in the cerebellar nuclei
title_sort synaptic mechanisms for associative learning in the cerebellar nuclei
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662440/
https://www.ncbi.nlm.nih.gov/pubmed/37985778
http://dx.doi.org/10.1038/s41467-023-43227-w
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