Evidence map›Paper›PMID 33128000›Full record

ArticleCommunications biology2020

Cellular-resolution mapping uncovers spatial adaptive filtering at the rat cerebellum input stage.

Stefano Casali, Marialuisa Tognolina, Daniela Gandolfi, Jonathan Mapelli, Egidio D'Angelo

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In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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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

5 authors.

Stefano CasaliDepartment of Brain and Behavioral Sciences, University of Pavia, I-27100, Pavia, Italy.
Marialuisa TognolinaDepartment of Brain and Behavioral Sciences, University of Pavia, I-27100, Pavia, Italy.
Daniela GandolfiDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, I-41125, Modena, Italy.
Jonathan MapelliDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, I-41125, Modena, Italy.ORCID 0000-0002-0381-1576
Egidio D'AngeloDepartment of Brain and Behavioral Sciences, University of Pavia, I-27100, Pavia, Italy. dangelo@unipv.it.ORCID 0000-0002-6007-7187

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term synaptic plasticity is thought to provide the substrate for adaptive computation in brain circuits but very little is known about its spatiotemporal organization. Here, we combined multi-spot two-photon laser microscopy in rat cerebellar slices with realistic modeling to map the distribution of plasticity in multi-neuronal units of the cerebellar granular layer. The units, composed by ~300 neurons activated by ~50 mossy fiber glomeruli, showed long-term potentiation concentrated in the core and long-term depression in the periphery. This plasticity was effectively accounted for by an NMDA receptor and calcium-dependent induction rule and was regulated by the inhibitory Golgi cell loops. Long-term synaptic plasticity created effective spatial filters tuning the time-delay and gain of spike retransmission at the cerebellum input stage and provided a plausible basis for the spatiotemporal recoding of input spike patterns anticipated by the motor learning theory.

Indexed as

AnimalsCalciumCerebellumFemaleLong-Term PotentiationMaleMicroscopy, ConfocalModels, NeurologicalNeuronal PlasticityNeuronsRats, WistarReceptors, N-Methyl-D-AspartateReproducibility of ResultsSynaptic TransmissionCalciumReceptors, N-Methyl-D-Aspartate

Identifiers

PMID33128000
PMCPMC7599228

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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.