Evidence map›Paper›PMID 29305531›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Nonselective Wiring Accounts for Red-Green Opponency in Midget Ganglion Cells of the Primate Retina.

Lauren E Wool, Joanna D Crook, John B Troy, Orin S Packer, Qasim Zaidi, Dennis M Dacey

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

37 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Review
  3. Approaching a connectome of the human foveal retina.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. Article
  6. Connectome of a human foveal retina.bioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Article
  9. A circuit motif for color in the human foveal retina.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Temporal Sensitivity for Achromatic and Chromatic Flicker across the Visual Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  11. Cone-Opponent Ganglion Cells in the Primate Fovea Tuned to Noncardinal Color Directions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Comparative connectomics reveals noncanonical wiring for color vision in human foveal retina.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Gaining the system: limits to compensating color deficiencies through post-receptoral gain changes.Journal of the Optical Society of America. A, Optics, image science, and vision · 2023
    Article
  18. Article
  19. Eye drift during fixation predicts visual acuity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  20. Article
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

6 authors at 3 institutions in 1 country.

Lauren E WoolState University of New York College of Optometry, Graduate Center for Vision Research, New York, New York 10036.ORCID 0000-0002-2955-2576
Joanna D CrookUniversity of Washington, Department of Biological Structure and the Washington National Primate Research Center, Seattle, Washington 98195, and.
John B TroyNorthwestern University, Department of Biomedical Engineering, McCormick School of Engineering, Evanston, Illinois 60208.ORCID 0000-0002-2504-6174
Orin S PackerUniversity of Washington, Department of Biological Structure and the Washington National Primate Research Center, Seattle, Washington 98195, and.
Qasim ZaidiState University of New York College of Optometry, Graduate Center for Vision Research, New York, New York 10036.ORCID 0000-0002-1300-2879
Dennis M DaceyUniversity of Washington, Department of Biological Structure and the Washington National Primate Research Center, Seattle, Washington 98195, and dmd@uw.edu.
University of Washington · USThe Graduate Center, CUNY · USNorthwestern University · US

Funding

Washington National Primate Research CenterP51OD010425 · OD · UNIVERSITY OF WASHINGTON · PI Mari Ostendorf · 2012 to 2026
$201.8M
YILMA SIV VACCINIA VACCINE TRIALP51RR000166 · NCRR · UNIVERSITY OF WASHINGTON · PI BAILLIE, THOMAS ALLAN · 1985 to 2011
$161.1M
Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI JAMES Bryant HURLEY · 1985 to 2026
$23.5M
SYNAPTIC INPUTS TO RETINAL GANGLION CELLSR01EY006678 · NEI · UNIVERSITY OF WASHINGTON · PI DACEY, DENNIS MICHAEL · 1986 to 2019
$8.2M
NEURAL BASIS OF SHAPE FROM TEXTURER01EY013312 · NEI · STATE COLLEGE OF OPTOMETRY · PI ZAIDI, QASIM · 2001 to 2015
$3.8M
MECHANISMS OF COLOR DETECTION, INDUCTION, AND ADAPTATIONR01EY007556 · NEI · STATE COLLEGE OF OPTOMETRY · PI ZAIDI, QASIM · 1993 to 2010
$2.4M
NCRR NIH HHS P51 RR000166NEI NIH HHS P30 EY001730NEI NIH HHS R01 EY006678NEI NIH HHS R01 EY007556NEI NIH HHS R01 EY013312NIH HHS P51 OD010425
6 · The paper itself

Abstract

In primate retina, "red-green" color coding is initiated when signals originating in long (L) and middle (M) wavelength-sensitive cone photoreceptors interact antagonistically. The center-surround receptive field of "midget" ganglion cells provides the neural substrate for L versus M cone-opponent interaction, but the underlying circuitry remains unsettled, centering around the longstanding question of whether specialized cone wiring is present. To address this question, we measured the strength, sign, and spatial tuning of L- and M-cone input to midget receptive fields in the peripheral retina of macaque primates of either sex. Consistent with previous work, cone opponency arose when one of the cone types showed a stronger connection to the receptive field center than to the surround. We implemented a difference-of-Gaussians spatial receptive field model, incorporating known biology of the midget circuit, to test whether physiological responses we observed in real cells could be captured entirely by anatomical nonselectivity. When this model sampled nonselectively from a realistic cone mosaic, it accurately reproduced key features of a cone-opponent receptive field structure, and predicted both the variability and strength of cone opponency across the retina. The model introduced here is consistent with abundant anatomical evidence for nonselective wiring, explains both local and global properties of the midget population, and supports a role in their multiplexing of spatial and color information. It provides a neural basis for human chromatic sensitivity across the visual field, as well as the maintenance of normal color vision despite significant variability in the relative number of L and M cones across individuals.

Indexed as

AnimalsCell SizeColor PerceptionColor VisionFemaleMacaca fascicularisMacaca mulattaMacaca nemestrinaMaleModels, NeurologicalNerve NetNormal DistributionPhotic StimulationRetinaRetinal Cone Photoreceptor CellsRetinal Ganglion Cellscircuitrycolorganglion cellprimateretinavision

Identifiers

PMID29305531
PMCPMC5815352
OpenAlexW2782440617

What OpenQuestion holds

Textmetadata
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.