Evidence map›Paper›PMID 33973524›Full record

ArticleeLife2021

Differential spatiotemporal development of Purkinje cell populations and cerebellum-dependent sensorimotor behaviors.

Gerrit Cornelis Beekhof, Catarina Osório, Joshua J White, Scott van Zoomeren, Hannah van der Stok, Bilian Xiong, Ingo Hms Nettersheim, Willem Ashwin Mak, Marit Runge, Francesca Romana Fiocchi and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 60 citations in OpenAlex.

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  14. More Than a Small Brain: The Importance of Studying Neural Function during Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  15. Review
  16. Cerebellar Purkinje Cells Control Posture in Larval Zebrafish (bioRxiv : the preprint server for biology · 2024
    Article
  17. Review
  18. PP2B-Dependent Cerebellar Plasticity Sets the Amplitude of the Vestibulo-ocular Reflex during Juvenile Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  19. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 2 countries.

Gerrit Cornelis Beekhof *Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-3038-5023
Catarina Osório *Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-5228-0599
Joshua J WhiteDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-6218-623X
Scott van ZoomerenDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.
Hannah van der StokDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-4134-4075
Bilian XiongDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.
Ingo Hms NettersheimDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0001-5207-5328
Willem Ashwin MakDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.
Marit RungeDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.
Francesca Romana FiocchiDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.
Henk-Jan BoeleDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.
Freek E HoebeekDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.
Martijn SchonewilleDepartment of Neuroscience, Erasmus MC, Rotterdam, Netherlands.ORCID 0000-0002-2675-1393
Erasmus MC · NLPrinceton University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Action PotentialsAnimalsAnimals, NewbornAxonsCerebellumFemaleMaleMiceMice, Inbred C57BLPurkinje Cellsbehaviorcerebellumdevelopmental biologyelectrophysiologymorphologymouseneurosciencePurkinje cellZebrinII

Identifiers

PMID33973524
PMCPMC8195607
OpenAlexW3162451065

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.