Evidence map›Paper›PMID 31160566›Full record

ArticleNature communications2019

Neural mechanisms of contextual modulation in the retinal direction selective circuit.

Xiaolin Huang, Melissa Rangel, Kevin L Briggman, Wei Wei

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Diverse and dynamic influences of saccades on visual representations in the mouse superior colliculus.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Retinal ganglion cells encode the direction of motion outside their classical receptive field.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Compartmentalized pooling generates orientation selectivity in wide-field amacrine cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Review
  9. Article
  10. Acetylcholine Promotes Directionally Biased Glutamatergic Retinal Waves.bioRxiv : the preprint server for biology · 2023
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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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

4 authors at 2 institutions in 2 countries.

Xiaolin HuangDepartment of Neurobiology, The University of Chicago, Chicago, IL, 60637, USA.ORCID http://orcid.org/0000-0001-7367-8347
Melissa RangelDepartment of Computational Neuroethology, Center of Advanced European Studies and Research (caesar), Bonn, 53175, Germany.
Kevin L BriggmanDepartment of Computational Neuroethology, Center of Advanced European Studies and Research (caesar), Bonn, 53175, Germany.
Wei WeiDepartment of Neurobiology, The University of Chicago, Chicago, IL, 60637, USA. weiw@uchicago.edu.
Center of Advanced European Studies and Research · DEUniversity of Chicago · US

Funding

Circuit mechanisms for encoding naturalistic motion in the mammalian retinaR01NS109990 · NINDS · UNIVERSITY OF CHICAGO · PI WEI, WEI · 2018 to 2022
$3.3M
Synaptic basis of motion detection in the retinaR01EY024016 · NEI · UNIVERSITY OF CHICAGO · PI WEI, WEI · 2014 to 2018
$1.9M
NEI NIH HHS R01 EY024016NINDS NIH HHS R01 NS109990
6 · The paper itself

Abstract

Contextual modulation of neuronal responses by surrounding environments is a fundamental attribute of sensory processing. In the mammalian retina, responses of On-Off direction selective ganglion cells (DSGCs) are modulated by motion contexts. However, the underlying mechanisms are unknown. Here, we show that posterior-preferring DSGCs (pDSGCs) are sensitive to discontinuities of moving contours owing to contextually modulated cholinergic excitation from starburst amacrine cells (SACs). Using a combination of synapse-specific genetic manipulations, patch clamp electrophysiology and connectomic analysis, we identified distinct circuit motifs upstream of On and Off SACs that are required for the contextual modulation of pDSGC activity for bright and dark contrasts. Furthermore, our results reveal a class of wide-field amacrine cells (WACs) with straight, unbranching dendrites that function as "continuity detectors" of moving contours. Therefore, divergent circuit motifs in the On and Off pathways extend the information encoding of On-Off DSGCs beyond their direction selectivity during complex stimuli.

Indexed as

AcetylcholineAmacrine CellsAnimalsConnectomeDendritesgamma-Aminobutyric AcidGlutamic AcidMiceMotion PerceptionPatch-Clamp TechniquesReceptors, GABA-ARetinal Ganglion CellsSynapsesVision, OcularVisual PerceptionAcetylcholineGabra2 protein, mousegamma-Aminobutyric AcidGlutamic AcidReceptors, GABA-A

Identifiers

PMID31160566
PMCPMC6547848
OpenAlexW2948335627

What OpenQuestion holds

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LicenceCC BY
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.