Evidence map›Paper›PMID 25821914›Full record

ArticleNature neuroscience2015

Synaptic diversity enables temporal coding of coincident multisensory inputs in single neurons.

François P Chabrol, Alexander Arenz, Martin T Wiechert, Troy W Margrie, David A DiGregorio

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed
15.2field-weighted citation impact, top 1% 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

139 citing papers in PubMed, 211 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Effects of Short-Term Synaptic Plasticity in Feedforward Inhibitory Circuits on Cerebellar Responses to Repetitive Sensory Input.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

François P Chabrol1] Institut Pasteur, Unit of Dynamic Neuronal Imaging, Paris, France. [2] CNRS UMR 3571, Genes, Synapses and Cognition, Institut Pasteur, Paris, France.
Alexander Arenz1] Division of Neurophysiology, MRC National Institute for Medical Research, Mill Hill, London, UK. [2] Max Planck Institute of Neurobiology, Department Circuits - Computation - Models, Martinsried, Germany.
Martin T Wiechert1] CNRS UMR 3571, Genes, Synapses and Cognition, Institut Pasteur, Paris, France. [2] Laboratory for Perception and Memory, Institut Pasteur, Paris, France.
Troy W Margrie1] Division of Neurophysiology, MRC National Institute for Medical Research, Mill Hill, London, UK. [2] Sainsbury Wellcome Centre for Neural Circuits and Behaviour, University College London, London, UK.
David A DiGregorio1] Institut Pasteur, Unit of Dynamic Neuronal Imaging, Paris, France. [2] CNRS UMR 3571, Genes, Synapses and Cognition, Institut Pasteur, Paris, France.
Centre National de la Recherche Scientifique · FRGènes, synapses et cognition · FRInstitut Pasteur · FR

Funding

Medical Research Council MC_U117597156Medical Research Council MC_U1175975156Wellcome Trust 096436
6 · The paper itself

Abstract

The ability of the brain to rapidly process information from multiple pathways is critical for reliable execution of complex sensory-motor behaviors, yet the cellular mechanisms underlying a neuronal representation of multimodal stimuli are poorly understood. Here we explored the possibility that the physiological diversity of mossy fiber (MF) to granule cell (GC) synapses in the mouse vestibulocerebellum may contribute to the processing of coincident multisensory information at the level of individual GCs. We found that the strength and short-term dynamics of individual MF-GC synapses can act as biophysical signatures for primary vestibular, secondary vestibular and visual input pathways. Most GCs receive inputs from different modalities, which, when coactivated, produced enhanced GC firing rates and distinct first spike latencies. Thus, pathway-specific synaptic response properties permit temporal coding of correlated multisensory inputs by single GCs, thereby enriching sensory representation and facilitating pattern separation.

Indexed as

AnimalsCerebellumDendritesDiscrimination, PsychologicalExcitatory Postsynaptic PotentialsKinesthesisMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicNerve FibersNerve NetNeuronsPatch-Clamp TechniquesPattern Recognition, VisualPhotic Stimulation

Identifiers

PMID25821914
PMCPMC4413433
OpenAlexW2047527379

What OpenQuestion holds

Textmetadata
LicenceTDM
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.