Cargando…

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;...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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
_version_ 1783706526617174016
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
work_keys_str_mv AT beekhofgerritcornelis differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT osoriocatarina differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT whitejoshuaj differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT vanzoomerenscott differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT vanderstokhannah differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT xiongbilian differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT nettersheimingohms differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT makwillemashwin differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT rungemarit differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT fiocchifrancescaromana differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT boelehenkjan differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT hoebeekfreeke differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors
AT schonewillemartijn differentialspatiotemporaldevelopmentofpurkinjecellpopulationsandcerebellumdependentsensorimotorbehaviors