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Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner

INTRODUCTION: The cerebellum is organized into functional regions each dedicated to process different motor or sensory inputs for controlling different locomotor behaviors. This functional regionalization is prominent in the evolutionary conserved single-cell layered Purkinje cell (PC) population. F...

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Autores principales: Dorigo, Alessandro, Valishetti, Komali, Hetsch, Florian, Matsui, Hideaki, Meier, Jochen C., Namikawa, Kazuhiko, Köster, Reinhard W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174242/
https://www.ncbi.nlm.nih.gov/pubmed/37181649
http://dx.doi.org/10.3389/fnmol.2023.1166900
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author Dorigo, Alessandro
Valishetti, Komali
Hetsch, Florian
Matsui, Hideaki
Meier, Jochen C.
Namikawa, Kazuhiko
Köster, Reinhard W.
author_facet Dorigo, Alessandro
Valishetti, Komali
Hetsch, Florian
Matsui, Hideaki
Meier, Jochen C.
Namikawa, Kazuhiko
Köster, Reinhard W.
author_sort Dorigo, Alessandro
collection PubMed
description INTRODUCTION: The cerebellum is organized into functional regions each dedicated to process different motor or sensory inputs for controlling different locomotor behaviors. This functional regionalization is prominent in the evolutionary conserved single-cell layered Purkinje cell (PC) population. Fragmented gene expression domains suggest a genetic organization of PC layer regionalization during cerebellum development. However, the establishment of such functionally specific domains during PC differentiation remained elusive. METHODS AND RESULTS: We show the progressive emergence of functional regionalization of PCs from broad responses to spatially restricted regions in zebrafish by means of in vivo Ca2+-imaging during stereotypic locomotive behavior. Moreover, we reveal that formation of new dendritic spines during cerebellar development using in vivo imaging parallels the time course of functional domain development. Pharmacological as well as cell-type specific optogenetic inhibition of PC neuronal activity results in reduced PC dendritic spine density and an altered stagnant pattern of functional domain formation in the PC layer. DISCUSSION: Hence, our study suggests that functional regionalization of the PC layer is driven by physiological activity of maturing PCs themselves.
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spelling pubmed-101742422023-05-12 Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner Dorigo, Alessandro Valishetti, Komali Hetsch, Florian Matsui, Hideaki Meier, Jochen C. Namikawa, Kazuhiko Köster, Reinhard W. Front Mol Neurosci Neuroscience INTRODUCTION: The cerebellum is organized into functional regions each dedicated to process different motor or sensory inputs for controlling different locomotor behaviors. This functional regionalization is prominent in the evolutionary conserved single-cell layered Purkinje cell (PC) population. Fragmented gene expression domains suggest a genetic organization of PC layer regionalization during cerebellum development. However, the establishment of such functionally specific domains during PC differentiation remained elusive. METHODS AND RESULTS: We show the progressive emergence of functional regionalization of PCs from broad responses to spatially restricted regions in zebrafish by means of in vivo Ca2+-imaging during stereotypic locomotive behavior. Moreover, we reveal that formation of new dendritic spines during cerebellar development using in vivo imaging parallels the time course of functional domain development. Pharmacological as well as cell-type specific optogenetic inhibition of PC neuronal activity results in reduced PC dendritic spine density and an altered stagnant pattern of functional domain formation in the PC layer. DISCUSSION: Hence, our study suggests that functional regionalization of the PC layer is driven by physiological activity of maturing PCs themselves. Frontiers Media S.A. 2023-04-27 /pmc/articles/PMC10174242/ /pubmed/37181649 http://dx.doi.org/10.3389/fnmol.2023.1166900 Text en Copyright © 2023 Dorigo, Valishetti, Hetsch, Matsui, Meier, Namikawa and Köster. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Dorigo, Alessandro
Valishetti, Komali
Hetsch, Florian
Matsui, Hideaki
Meier, Jochen C.
Namikawa, Kazuhiko
Köster, Reinhard W.
Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner
title Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner
title_full Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner
title_fullStr Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner
title_full_unstemmed Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner
title_short Functional regionalization of the differentiating cerebellar Purkinje cell population occurs in an activity-dependent manner
title_sort functional regionalization of the differentiating cerebellar purkinje cell population occurs in an activity-dependent manner
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174242/
https://www.ncbi.nlm.nih.gov/pubmed/37181649
http://dx.doi.org/10.3389/fnmol.2023.1166900
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