Evidence map›Paper›PMID 29937281›Full record

ArticleNeuron2018

How Diverse Retinal Functions Arise from Feedback at the First Visual Synapse.

Antonia Drinnenberg, Felix Franke, Rei K Morikawa, Josephine Jüttner, Daniel Hillier, Peter Hantz, Andreas Hierlemann, Rava Azeredo da Silveira, Botond Roska

Abstract read
In one paragraph

Article in Neuron, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

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  10. Altered Functional Responses of the Retina in B6 Albino Tyrc/c Mice.Investigative ophthalmology & visual science · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Antonia DrinnenbergFriedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland; Institute of Molecular and Clinical Ophthalmology Basel, 4031 Basel, Switzerland; Faculty of Natural Sciences, University of Basel, 4003 Basel, Switzerland.
Felix FrankeBio Engineering Laboratory, Department of Biosystems Science and Engineering of ETH Zurich, 4058 Basel, Switzerland.
Rei K MorikawaFriedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland; Institute of Molecular and Clinical Ophthalmology Basel, 4031 Basel, Switzerland.
Josephine JüttnerFriedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland; Institute of Molecular and Clinical Ophthalmology Basel, 4031 Basel, Switzerland.
Daniel HillierFriedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland; Institute of Molecular and Clinical Ophthalmology Basel, 4031 Basel, Switzerland.
Peter HantzFriedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland.
Andreas HierlemannBio Engineering Laboratory, Department of Biosystems Science and Engineering of ETH Zurich, 4058 Basel, Switzerland.
Rava Azeredo da SilveiraDepartment of Physics, Ecole Normale Supérieure, 75005 Paris, France; Laboratoire de Physique Statistique, École Normale Supérieure, PSL Research University; Université Paris Diderot Sorbonne Paris-Cité; Sorbonne Universités UPMC Univ Paris 06; CNRS, 75005 Paris, France; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08544, USA. Electronic address: rava@ens.fr.
Botond RoskaFriedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland; Institute of Molecular and Clinical Ophthalmology Basel, 4031 Basel, Switzerland; Department of Ophthalmology, University of Basel, 4031 Basel, Switzerland. Electronic address: botond.roska@iob.ch.

Funding

European Research Council 267351Swiss National Science Foundation 141801
6 · The paper itself

Abstract

Many brain regions contain local interneurons of distinct types. How does an interneuron type contribute to the input-output transformations of a given brain region? We addressed this question in the mouse retina by chemogenetically perturbing horizontal cells, an interneuron type providing feedback at the first visual synapse, while monitoring the light-driven spiking activity in thousands of ganglion cells, the retinal output neurons. We uncovered six reversible perturbation-induced effects in the response dynamics and response range of ganglion cells. The effects were enhancing or suppressive, occurred in different response epochs, and depended on the ganglion cell type. A computational model of the retinal circuitry reproduced all perturbation-induced effects and led us to assign specific functions to horizontal cells with respect to different ganglion cell types. Our combined experimental and theoretical work reveals how a single interneuron type can differentially shape the dynamical properties of distinct output channels of a brain region.

Indexed as

FeedbackAnimalsCalciumInterneuronsMiceModels, NeurologicalPhotoreceptor Cells, VertebrateRetinal Bipolar CellsRetinal Ganglion CellsRetinal Horizontal CellsSynapsesVision, OcularCalciumcell typecomputationganglion cellhorizontal cellinhibitioninterneuronmodelneuronal circuitnon-linear neural processingretina

Identifiers

PMID29937281
PMCPMC6101199

What OpenQuestion holds

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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.