Evidence map›Paper›PMID 20724365›Full record

ArticleThe Journal of physiology2010

Encoding of whisker input by cerebellar Purkinje cells.

Laurens W J Bosman, Sebastiaan K E Koekkoek, Jöel Shapiro, Bianca F M Rijken, Froukje Zandstra, Barry van der Ende, Cullen B Owens, Jan-Willem Potters, Jornt R de Gruijl, Tom J H Ruigrok and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
4.3field-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

76 citing papers in PubMed, 131 citations in OpenAlex.

  1. Representations of Subsecond Duration-Based Timing by Complex Spike Synchrony in Cerebellar Purkinje Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  4. Review
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  8. Cerebellar control of targeted tongue movements.The Journal of physiology · 2025
    Article
  9. GlyT2-Positive Interneurons Regulate Timing and Variability of Information Transfer in a Cerebellar-Behavioral Loop.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  10. Heterogeneity in Slow Synaptic Transmission Diversifies Purkinje Cell Timing.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  11. Article
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  15. Overexpression of the autism candidate geneFrontiers in cellular neuroscience · 2023
    Article
  16. Article
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  20. Synchronous spiking of cerebellar Purkinje cells during control of movements.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article

16 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Laurens W J BosmanDepartment of Neuroscience, Erasmus MC, Rotterdam, The Netherlands.
Sebastiaan K E Koekkoek
Jöel Shapiro
Bianca F M Rijken
Froukje Zandstra
Barry van der Ende
Cullen B Owens
Jan-Willem Potters
Jornt R de Gruijl
Tom J H Ruigrok
Chris I De Zeeuw
Erasmus MC · NLErasmus University Rotterdam · NLRoyal Academy of Art · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cerebellar cortex is crucial for sensorimotor integration. Sensorimotor inputs converge on cerebellar Purkinje cells via two afferent pathways: the climbing fibre pathway triggering complex spikes, and the mossy fibre–parallel fibre pathway, modulating the simple spike activities of Purkinje cells. We used, for the first time, the mouse whisker system as a model system to study the encoding of somatosensory input by Purkinje cells.We show that most Purkinje cells in ipsilateral crus 1 and crus 2 of awake mice respond to whisker stimulation with complex spike and/or simple spike responses. Single-whisker stimulation in anaesthetised mice revealed that the receptive fields of complex spike and simple spike responses were strikingly different. Complex spike responses, which proved to be sensitive to the amplitude, speed and direction of whisker movement, were evoked by only one or a few whiskers. Simple spike responses, which were not affected by the direction of movement, could be evoked by many individual whiskers. The receptive fields of Purkinje cells were largely intermingled, and we suggest that this facilitates the rapid integration of sensory inputs from different sources. Furthermore, we describe that individual Purkinje cells, at least under anaesthesia, may be bound in two functional ensembles based on the receptive fields and the synchrony of the complex spike and simple spike responses. The ‘complex spike ensembles’ were oriented in the sagittal plane, following the anatomical organization of the climbing fibres, while the ‘simple spike ensembles’ were oriented in the transversal plane, as are the beams of parallel fibres.

Indexed as

Afferent PathwaysAnesthesiaAnimalsCerebellumElectrodes, ImplantedElectrophysiological PhenomenaMaleMiceMice, Inbred C57BLNerve FibersPhysical StimulationPurkinje CellsSensationSynaptic TransmissionVibrissae

Identifiers

PMID20724365
PMCPMC2998225
OpenAlexW1592554002

What OpenQuestion holds

Textmetadata
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.