Evidence map›Paper›PMID 38008788›Full record

ArticleNature communications2023

Modular interneuron circuits control motion sensitivity in the mouse retina.

Andrew Jo, Sercan Deniz, Suraj Cherian, Jian Xu, Daiki Futagi, Steven H DeVries, Yongling Zhu

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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

7 authors.

Andrew Jo *Departments of Ophthalmology and Neuroscience, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Sercan Deniz *Departments of Ophthalmology and Neuroscience, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Suraj CherianDepartments of Ophthalmology and Neuroscience, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Jian XuDepartments of Ophthalmology and Neuroscience, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Daiki FutagiDepartments of Ophthalmology and Neuroscience, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.ORCID 0000-0003-3972-2054
Steven H DeVriesDepartments of Ophthalmology and Neuroscience, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.ORCID 0000-0002-9636-4196
Yongling ZhuDepartments of Ophthalmology and Neuroscience, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA. yongling-zhu@northwestern.edu.ORCID 0000-0002-2527-402X

Funding

FUNCTION OF BASAL SYNAPSES AT PHOTORECEPTORSR01EY012141 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Steven H DeVries · 1999 to 2026
$8.5M
Signal Processing in the Inner RetinaR01EY018204 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DEVRIES, STEVEN H, ZHU, YONGLING · 2007 to 2024
$6.4M
Cell types and functional circuitry in the retinaR01EY030169 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI YONGLING ZHU · 2019 to 2026
$3.1M
Regulation of kainate receptor expression in cone bipolar cellsR01EY032506 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CONTRACTOR, ANIS, DEVRIES, STEVEN H · 2022 to 2025
$1.7M
Visual Sciences T32T32EY025202 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Gregory William Schwartz · 2015 to 2026
$1.4M
Intersectional genetic dissection of inner retinal circuitsF31EY031985 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JO, ANDREW OH · 2020 to 2022
$127k
NEI NIH HHS F31 EY031985NEI NIH HHS R01 EY012141NEI NIH HHS R01 EY018204NEI NIH HHS R01 EY030169NEI NIH HHS R01 EY032506NEI NIH HHS T32 EY025202
6 · The paper itself

Abstract

Neural computations arise from highly precise connections between specific types of neurons. Retinal ganglion cells (RGCs) with similar stratification patterns are positioned to receive similar inputs but often display different response properties. In this study, we used intersectional mouse genetics to achieve single-cell type labeling and identified an object motion sensitive (OMS) AC type, COMS-AC(counter-OMS AC). Optogenetic stimulation revealed that COMS-AC makes glycinergic synapses with the OMS-insensitive HD2p-RGC, while chemogenetic inactivation showed that COMS-AC provides inhibitory control to HD2p-RGC during local motion. This local inhibition, combined with the inhibitory drive from TH2-AC during global motion, explains the OMS-insensitive feature of HD2p-RGC. In contrast, COMS-AC fails to make synapses with W3(UHD)-RGC, allowing it to exhibit OMS under the control of VGlut3-AC and TH2-AC. These findings reveal modular interneuron circuits that endow structurally similar RGC types with different responses and present a mechanism for redundancy-reduction in the retina to expand coding capacity.

Indexed as

RetinaRetinal Ganglion CellsAnimalsInterneuronsMiceSynapsesSynaptic Transmission

Identifiers

PMID38008788
PMCPMC10679153

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.