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Cerebellar contributions to a brainwide network for flexible behavior in mice

The cerebellum regulates nonmotor behavior, but the routes of influence are not well characterized. Here we report a necessary role for the posterior cerebellum in guiding a reversal learning task through a network of diencephalic and neocortical structures, and in flexibility of free behavior. Afte...

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Autores principales: Verpeut, Jessica L., Bergeler, Silke, Kislin, Mikhail, William Townes, F., Klibaite, Ugne, Dhanerawala, Zahra M., Hoag, Austin, Janarthanan, Sanjeev, Jung, Caroline, Lee, Junuk, Pisano, Thomas J., Seagraves, Kelly M., Shaevitz, Joshua W., Wang, Samuel S.-H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241932/
https://www.ncbi.nlm.nih.gov/pubmed/37277453
http://dx.doi.org/10.1038/s42003-023-04920-0
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author Verpeut, Jessica L.
Bergeler, Silke
Kislin, Mikhail
William Townes, F.
Klibaite, Ugne
Dhanerawala, Zahra M.
Hoag, Austin
Janarthanan, Sanjeev
Jung, Caroline
Lee, Junuk
Pisano, Thomas J.
Seagraves, Kelly M.
Shaevitz, Joshua W.
Wang, Samuel S.-H.
author_facet Verpeut, Jessica L.
Bergeler, Silke
Kislin, Mikhail
William Townes, F.
Klibaite, Ugne
Dhanerawala, Zahra M.
Hoag, Austin
Janarthanan, Sanjeev
Jung, Caroline
Lee, Junuk
Pisano, Thomas J.
Seagraves, Kelly M.
Shaevitz, Joshua W.
Wang, Samuel S.-H.
author_sort Verpeut, Jessica L.
collection PubMed
description The cerebellum regulates nonmotor behavior, but the routes of influence are not well characterized. Here we report a necessary role for the posterior cerebellum in guiding a reversal learning task through a network of diencephalic and neocortical structures, and in flexibility of free behavior. After chemogenetic inhibition of lobule VI vermis or hemispheric crus I Purkinje cells, mice could learn a water Y-maze but were impaired in ability to reverse their initial choice. To map targets of perturbation, we imaged c-Fos activation in cleared whole brains using light-sheet microscopy. Reversal learning activated diencephalic and associative neocortical regions. Distinctive subsets of structures were altered by perturbation of lobule VI (including thalamus and habenula) and crus I (including hypothalamus and prelimbic/orbital cortex), and both perturbations influenced anterior cingulate and infralimbic cortex. To identify functional networks, we used correlated variation in c-Fos activation within each group. Lobule VI inactivation weakened within-thalamus correlations, while crus I inactivation divided neocortical activity into sensorimotor and associative subnetworks. In both groups, high-throughput automated analysis of whole-body movement revealed deficiencies in across-day behavioral habituation to an open-field environment. Taken together, these experiments reveal brainwide systems for cerebellar influence that affect multiple flexible responses.
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spelling pubmed-102419322023-06-07 Cerebellar contributions to a brainwide network for flexible behavior in mice Verpeut, Jessica L. Bergeler, Silke Kislin, Mikhail William Townes, F. Klibaite, Ugne Dhanerawala, Zahra M. Hoag, Austin Janarthanan, Sanjeev Jung, Caroline Lee, Junuk Pisano, Thomas J. Seagraves, Kelly M. Shaevitz, Joshua W. Wang, Samuel S.-H. Commun Biol Article The cerebellum regulates nonmotor behavior, but the routes of influence are not well characterized. Here we report a necessary role for the posterior cerebellum in guiding a reversal learning task through a network of diencephalic and neocortical structures, and in flexibility of free behavior. After chemogenetic inhibition of lobule VI vermis or hemispheric crus I Purkinje cells, mice could learn a water Y-maze but were impaired in ability to reverse their initial choice. To map targets of perturbation, we imaged c-Fos activation in cleared whole brains using light-sheet microscopy. Reversal learning activated diencephalic and associative neocortical regions. Distinctive subsets of structures were altered by perturbation of lobule VI (including thalamus and habenula) and crus I (including hypothalamus and prelimbic/orbital cortex), and both perturbations influenced anterior cingulate and infralimbic cortex. To identify functional networks, we used correlated variation in c-Fos activation within each group. Lobule VI inactivation weakened within-thalamus correlations, while crus I inactivation divided neocortical activity into sensorimotor and associative subnetworks. In both groups, high-throughput automated analysis of whole-body movement revealed deficiencies in across-day behavioral habituation to an open-field environment. Taken together, these experiments reveal brainwide systems for cerebellar influence that affect multiple flexible responses. Nature Publishing Group UK 2023-06-05 /pmc/articles/PMC10241932/ /pubmed/37277453 http://dx.doi.org/10.1038/s42003-023-04920-0 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Verpeut, Jessica L.
Bergeler, Silke
Kislin, Mikhail
William Townes, F.
Klibaite, Ugne
Dhanerawala, Zahra M.
Hoag, Austin
Janarthanan, Sanjeev
Jung, Caroline
Lee, Junuk
Pisano, Thomas J.
Seagraves, Kelly M.
Shaevitz, Joshua W.
Wang, Samuel S.-H.
Cerebellar contributions to a brainwide network for flexible behavior in mice
title Cerebellar contributions to a brainwide network for flexible behavior in mice
title_full Cerebellar contributions to a brainwide network for flexible behavior in mice
title_fullStr Cerebellar contributions to a brainwide network for flexible behavior in mice
title_full_unstemmed Cerebellar contributions to a brainwide network for flexible behavior in mice
title_short Cerebellar contributions to a brainwide network for flexible behavior in mice
title_sort cerebellar contributions to a brainwide network for flexible behavior in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241932/
https://www.ncbi.nlm.nih.gov/pubmed/37277453
http://dx.doi.org/10.1038/s42003-023-04920-0
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