Evidence map›Paper›PMID 32169206›Full record

ArticleCurrent biology : CB2020

Temporal Sharpening of Sensory Responses by Layer V in the Mouse Primary Somatosensory Cortex.

Dania Vecchia, Riccardo Beltramo, Fabio Vallone, Ronan Chéreau, Angelo Forli, Manuel Molano-Mazón, Tanika Bawa, Noemi Binini, Claudio Moretti, Anthony Holtmaat and 2 more

Abstract read
In one paragraph

Article in Current biology : CB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 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

12 authors.

Dania VecchiaOptical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, 16163 Genova, Italy; Neural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy.
Riccardo BeltramoOptical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, 16163 Genova, Italy.
Fabio ValloneNeural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy.
Ronan ChéreauDepartment of Basic Neurosciences, Geneva University Neurocenter, Faculty of Medicine, University of Geneva, 1206 Geneva, Switzerland.
Angelo ForliOptical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, 16163 Genova, Italy; Neural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy.
Manuel Molano-MazónNeural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy; Neural Computation Laboratory, Center for Neuroscience and Cognitive Systems @UniTn, Istituto Italiano di Tecnologia, 38068 Rovereto, Italy.
Tanika BawaDepartment of Basic Neurosciences, Geneva University Neurocenter, Faculty of Medicine, University of Geneva, 1206 Geneva, Switzerland.
Noemi BininiOptical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, 16163 Genova, Italy; Neural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy.
Claudio MorettiOptical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, 16163 Genova, Italy; Neural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy.
Anthony HoltmaatDepartment of Basic Neurosciences, Geneva University Neurocenter, Faculty of Medicine, University of Geneva, 1206 Geneva, Switzerland.
Stefano PanzeriNeural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy; Neural Computation Laboratory, Center for Neuroscience and Cognitive Systems @UniTn, Istituto Italiano di Tecnologia, 38068 Rovereto, Italy.
Tommaso FellinOptical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, 16163 Genova, Italy; Neural Coding Laboratory, Istituto Italiano di Tecnologia, 16163 Genova and 38068 Rovereto, Italy. Electronic address: tommaso.fellin@iit.it.

Funding

Readout and control of spatiotemporal neuronal codes for behaviorU19NS107464 · NINDS · UNIVERSITY OF CHICAGO · PI SHOHAM, SHY · 2018 to 2022
$17.3M
The role of patterned activity in neuronal codes for behaviorU01NS090576 · NINDS · UNIVERSITY OF CHICAGO · PI FELLIN, TOMMASO, HISTED, MARK H · 2014 to 2016
$1.6M
NINDS NIH HHS U01 NS090576NINDS NIH HHS U19 NS107464
6 · The paper itself

Abstract

The timing of stimulus-evoked spikes encodes information about sensory stimuli. Here we studied the neural circuits controlling this process in the mouse primary somatosensory cortex. We found that brief optogenetic activation of layer V pyramidal cells just after whisker deflection modulated the membrane potential of neurons and interrupted their long-latency whisker responses, increasing their accuracy in encoding whisker deflection time. In contrast, optogenetic inhibition of layer V during either passive whisker deflection or active whisking decreased accuracy in encoding stimulus or touch time, respectively. Suppression of layer V pyramidal cells increased reaction times in a texture discrimination task. Moreover, two-color optogenetic experiments revealed that cortical inhibition was efficiently recruited by layer V stimulation and that it mainly involved activation of parvalbumin-positive rather than somatostatin-positive interneurons. Layer V thus performs behaviorally relevant temporal sharpening of sensory responses through circuit-specific recruitment of cortical inhibition.

Indexed as

Action PotentialsAnimalsMiceNeuronsSomatosensory CortexTime FactorsTouchTouch PerceptionVibrissaecortical layersGABAergic interneuronsparvalbuminsomatosensory cortexsomatostatinwhisking

Identifiers

PMID32169206
PMCPMC7198976

What OpenQuestion holds

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Registered trials

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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.