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Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors
Distinct populations of Purkinje cells (PCs) with unique molecular and connectivity features are at the core of the modular organization of the cerebellum. Previously, we showed that firing activity of PCs differs between ZebrinII-positive and ZebrinII-negative cerebellar modules (Zhou et al., 2014;...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195607/ https://www.ncbi.nlm.nih.gov/pubmed/33973524 http://dx.doi.org/10.7554/eLife.63668 |
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author | Beekhof, Gerrit Cornelis Osório, Catarina White, Joshua J van Zoomeren, Scott van der Stok, Hannah Xiong, Bilian Nettersheim, Ingo HMS Mak, Willem Ashwin Runge, Marit Fiocchi, Francesca Romana Boele, Henk-Jan Hoebeek, Freek E Schonewille, Martijn |
author_facet | Beekhof, Gerrit Cornelis Osório, Catarina White, Joshua J van Zoomeren, Scott van der Stok, Hannah Xiong, Bilian Nettersheim, Ingo HMS Mak, Willem Ashwin Runge, Marit Fiocchi, Francesca Romana Boele, Henk-Jan Hoebeek, Freek E Schonewille, Martijn |
author_sort | Beekhof, Gerrit Cornelis |
collection | PubMed |
description | Distinct populations of Purkinje cells (PCs) with unique molecular and connectivity features are at the core of the modular organization of the cerebellum. Previously, we showed that firing activity of PCs differs between ZebrinII-positive and ZebrinII-negative cerebellar modules (Zhou et al., 2014; Wu et al., 2019). Here, we investigate the timing and extent of PC differentiation during development in mice. We found that several features of PCs, including activity levels, dendritic arborization, axonal shape and climbing fiber input, develop differentially between nodular and anterior PC populations. Although all PCs show a particularly rapid development in the second postnatal week, anterior PCs typically have a prolonged physiological and dendritic maturation. In line herewith, younger mice exhibit attenuated anterior-dependent eyeblink conditioning, but faster nodular-dependent compensatory eye movement adaptation. Our results indicate that specific cerebellar regions have unique developmental timelines which match with their related, specific forms of cerebellum-dependent behaviors. |
format | Online Article Text |
id | pubmed-8195607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-81956072021-06-14 Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors Beekhof, Gerrit Cornelis Osório, Catarina White, Joshua J van Zoomeren, Scott van der Stok, Hannah Xiong, Bilian Nettersheim, Ingo HMS Mak, Willem Ashwin Runge, Marit Fiocchi, Francesca Romana Boele, Henk-Jan Hoebeek, Freek E Schonewille, Martijn eLife Developmental Biology Distinct populations of Purkinje cells (PCs) with unique molecular and connectivity features are at the core of the modular organization of the cerebellum. Previously, we showed that firing activity of PCs differs between ZebrinII-positive and ZebrinII-negative cerebellar modules (Zhou et al., 2014; Wu et al., 2019). Here, we investigate the timing and extent of PC differentiation during development in mice. We found that several features of PCs, including activity levels, dendritic arborization, axonal shape and climbing fiber input, develop differentially between nodular and anterior PC populations. Although all PCs show a particularly rapid development in the second postnatal week, anterior PCs typically have a prolonged physiological and dendritic maturation. In line herewith, younger mice exhibit attenuated anterior-dependent eyeblink conditioning, but faster nodular-dependent compensatory eye movement adaptation. Our results indicate that specific cerebellar regions have unique developmental timelines which match with their related, specific forms of cerebellum-dependent behaviors. eLife Sciences Publications, Ltd 2021-05-11 /pmc/articles/PMC8195607/ /pubmed/33973524 http://dx.doi.org/10.7554/eLife.63668 Text en © 2021, Beekhof 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 | Developmental Biology Beekhof, Gerrit Cornelis Osório, Catarina White, Joshua J van Zoomeren, Scott van der Stok, Hannah Xiong, Bilian Nettersheim, Ingo HMS Mak, Willem Ashwin Runge, Marit Fiocchi, Francesca Romana Boele, Henk-Jan Hoebeek, Freek E Schonewille, Martijn Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors |
title | Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors |
title_full | Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors |
title_fullStr | Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors |
title_full_unstemmed | Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors |
title_short | Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors |
title_sort | differential spatiotemporal development of purkinje cell populations and cerebellum-dependent sensorimotor behaviors |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195607/ https://www.ncbi.nlm.nih.gov/pubmed/33973524 http://dx.doi.org/10.7554/eLife.63668 |
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