Evidence map›Paper›PMID 24801624›Full record

ArticleVisual neuroscience2014

A synaptic signature for ON- and OFF-center parasol ganglion cells of the primate retina.

Joanna D Crook, Orin S Packer, Dennis M Dacey

Open access · greenAbstract read
In one paragraph

Article in Visual neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

23 citing papers in PubMed, 55 citations in OpenAlex.

  1. Frontiers in cell and developmental biology · 2025
    Review
  2. Article
  3. Diversity of Ganglion Cell Responses to Saccade-Like Image Shifts in the Primate Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  4. A deep neural network model of the primate superior colliculus for emotion recognition.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Convergence and Divergence of CRH Amacrine Cells in Mouse Retinal Circuitry.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  15. Article
  16. Article
  17. Synaptic Mechanisms Generating Orientation Selectivity in the ON Pathway of the Rabbit Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  18. Article
  19. Functional Circuitry of the Retina.Annual review of vision science · 2015
    Article
  20. Schizophrenia and the eye.Schizophrenia research. Cognition · 2015
    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

3 authors at 1 institution in 1 country.

Joanna D CrookDepartment of Biological Structure, University of Washington and the Washington National Primate Research Center (NPRC), Seattle, Washington.
Orin S PackerDepartment of Biological Structure, University of Washington and the Washington National Primate Research Center (NPRC), Seattle, Washington.
Dennis M DaceyDepartment of Biological Structure, University of Washington and the Washington National Primate Research Center (NPRC), Seattle, Washington.
University of Washington · US

Funding

YILMA SIV VACCINIA VACCINE TRIALP51RR000166 · NCRR · UNIVERSITY OF WASHINGTON · PI HU, SHIU-LOK · 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
VISUAL SCIENCES TRAINING PROGRAMT32EY007031 · NEI · UNIVERSITY OF WASHINGTON · PI Wyeth Daniel Bair, Anitha Pasupathy · 1985 to 2026
$6.1M
REGULATION OF THE OUTER BLOOD-RETINAL BARRIERF32EY007031 · NEI · YALE UNIVERSITY · PI WILT, STEVEN D · 1999 to 2000
$11k
EXPRESSION OF MYOTONIC DYSTROPHY PROTEIN KINASE IN LENSF32EY006778 · NEI · BAYLOR COLLEGE OF MEDICINE · PI JIN, SHIDA · 1996 to 1997
–
NCRR NIH HHS P51 RR000166NCRR NIH HHS RR00166NEI NIH HHS EY007031NEI NIH HHS EY01730NEI NIH HHS EY06778NEI NIH HHS F32 EY006778NEI NIH HHS F32 EY007031NEI NIH HHS P30 EY001730NEI NIH HHS R01 EY006678NEI NIH HHS T32 EY007031
6 · The paper itself

Abstract

In the primate retina, parasol ganglion cells contribute to the primary visual pathway via the magnocellular division of the lateral geniculate nucleus, display ON and OFF concentric receptive field structure, nonlinear spatial summation, and high achromatic temporal-contrast sensitivity. Parasol cells may be homologous to the alpha-Y cells of nonprimate mammals where evidence suggests that N-methyl-D-aspartate (NMDA) receptor-mediated synaptic excitation as well as glycinergic disinhibition play critical roles in contrast sensitivity, acting asymmetrically in OFF- but not ON-pathways. Here, light-evoked synaptic currents were recorded in the macaque monkey retina in vitro to examine the circuitry underlying parasol cell receptive field properties. Synaptic excitation in both ON and OFF types was mediated by NMDA as well as α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)/kainate glutamate receptors. The NMDA-mediated current-voltage relationship suggested high Mg2+ affinity such that at physiological potentials, NMDA receptors contributed ∼20% of the total excitatory conductance evoked by moderate stimulus contrasts and temporal frequencies. Postsynaptic inhibition in both ON and OFF cells was dominated by a large glycinergic "crossover" conductance, with a relatively small contribution from GABAergic feedforward inhibition. However, crossover inhibition was largely rectified, greatly diminished at low stimulus contrasts, and did not contribute, via disinhibition, to contrast sensitivity. In addition, attenuation of GABAergic and glycinergic synaptic inhibition left center-surround and Y-type receptive field structure and high temporal sensitivity fundamentally intact and clearly derived from modulation of excitatory bipolar cell output. Thus, the characteristic spatial and temporal-contrast sensitivity of the primate parasol cell arises presynaptically and is governed primarily by modulation of the large AMPA/kainate receptor-mediated excitatory conductance. Moreover, the negative feedback responsible for the receptive field surround must derive from a nonGABAergic mechanism.

Indexed as

AnimalsGABA AntagonistsIn Vitro TechniquesMacacaPhotic StimulationPresynaptic TerminalsReceptors, N-Methyl-D-AspartateRetinal Ganglion CellsSynapsesGABA AntagonistsReceptors, N-Methyl-D-Aspartate

Identifiers

PMID24801624
PMCPMC4503220
OpenAlexW2313348546

What OpenQuestion holds

Textmetadata
LicenceTDM
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.