Evidence map›Paper›PMID 25834063›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Broad thorny ganglion cells: a candidate for visual pursuit error signaling in the primate retina.

Christian Puller, Michael B Manookin, Jay Neitz, Fred Rieke, Maureen Neitz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
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  7. Frontiers in cell and developmental biology · 2025
    Review
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  15. Synaptic inputs to broad thorny ganglion cells in macaque retina.The Journal of comparative neurology · 2021
    Article
  16. Review
  17. 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

5 authors at 3 institutions in 2 countries.

Christian PullerDepartment of Ophthalmology, christian.puller@uni-oldenburg.de mneitz@uw.edu.
Michael B ManookinDepartment of Ophthalmology.
Jay NeitzDepartment of Ophthalmology.ORCID http://orcid.org/0000-0003-3877-6712
Fred RiekePhysiology and Biophysics Department, and Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98109.
Maureen NeitzDepartment of Ophthalmology, christian.puller@uni-oldenburg.de mneitz@uw.edu.ORCID http://orcid.org/0000-0002-5404-3343
Carl von Ossietzky Universität Oldenburg · DEOphthalmology Associates (United States) · USHoward Hughes Medical Institute · US

Funding

Washington National Primate Research CenterP51OD010425 · OD · UNIVERSITY OF WASHINGTON · PI Mari Ostendorf · 2012 to 2026
$201.8M
Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI Jay Neitz · 1985 to 2026
$23.5M
GENES AND VISUAL PIGMENTS OF RED/GREEN COLOR VISIONR01EY009303 · NEI · UNIVERSITY OF WASHINGTON · PI NEITZ, MAUREEN E · 1991 to 2013
$5.2M
BIOPHYSICAL MECHANISMS OF SINGLE PHOTON DETECTIONR01EY011850 · NEI · UNIVERSITY OF WASHINGTON · PI RIEKE, FREDERICK M · 1997 to 2015
$3.5M
Light encoding properties of wiry-type and starburst amacrine cells of the primatF32EY024507 · NEI · UNIVERSITY OF WASHINGTON · PI MANOOKIN, MICHAEL B · 2014 to 2014
$57k
Howard Hughes Medical InstituteNEI NIH HHS F32 EY024507NEI NIH HHS P30 EY001730NEI NIH HHS P30 EY01730NEI NIH HHS R01 EY009303NEI NIH HHS R01 EY011850NEI NIH HHS R01EY09303NEI NIH HHS R01 EY11850NIH HHS P51 OD010425
6 · The paper itself

Abstract

Functional analyses exist only for a few of the morphologically described primate ganglion cell types, and their correlates in other mammalian species remain elusive. Here, we recorded light responses of broad thorny cells in the whole-mounted macaque retina. They showed ON-OFF-center light responses that were strongly suppressed by stimulation of the receptive field surround. Spike responses were delayed compared with parasol ganglion cells and other ON-OFF cells, including recursive bistratified ganglion cells and A1 amacrine cells. The receptive field structure was shaped by direct excitatory synaptic input and strong presynaptic and postsynaptic inhibition in both ON and OFF pathways. The cells responded strongly to dark or bright stimuli moving either in or out of the receptive field, independent of the direction of motion. However, they did not show a maintained spike response either to a uniform background or to a drifting plaid pattern. These properties could be ideally suited for guiding movements involved in visual pursuit. The functional characteristics reported here permit the first direct cross-species comparison of putative homologous ganglion cell types. Based on morphological similarities, broad thorny ganglion cells have been proposed to be homologs of rabbit local edge detector ganglion cells, but we now show that the two cells have quite distinct physiological properties. Thus, our data argue against broad thorny cells as the homologs of local edge detector cells.

Indexed as

Action PotentialsAmacrine CellsAnimalsFemaleMacacaMaleMotion PerceptionPhotic StimulationPursuit, SmoothRetinaRetinal Ganglion CellsVisual FieldsVisual Pathwayseye movementsganglion cellslight responsesnonimage-forming visionprimate retina

Identifiers

PMID25834063
PMCPMC4381007
OpenAlexW2010857256

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.