Evidence map›Paper›PMID 36071126›Full record

ArticleScientific reports2022

Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina.

Andrea S Bordt, Sara S Patterson, James A Kuchenbecker, Marcus A Mazzaferri, Joel N Yearick, Emma R Yang, Judith Mosinger Ogilvie, Jay Neitz, David W Marshak

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Frontiers in cell and developmental biology · 2025
    Review
  4. Article
  5. 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

9 authors at 4 institutions in 1 country.

Andrea S BordtDepartment of Neurobiology and Anatomy, McGovern Medical School, Houston, TX, USA.
Sara S PattersonDepartment of Ophthalmology, University of Washington, Seattle, WA, USA.
James A KuchenbeckerDepartment of Ophthalmology, University of Washington, Seattle, WA, USA.
Marcus A MazzaferriDepartment of Ophthalmology, University of Washington, Seattle, WA, USA.
Joel N YearickDepartment of BioSciences, Rice University, Houston, TX, USA.
Emma R YangDepartment of BioSciences, Rice University, Houston, TX, USA.
Judith Mosinger OgilvieDepartment of Biology, Saint Louis University, Saint Louis, MO, USA.
Jay NeitzDepartment of Ophthalmology, University of Washington, Seattle, WA, USA.
David W MarshakDepartment of Neurobiology and Anatomy, McGovern Medical School, Houston, TX, USA. david.w.marshak@uth.tmc.edu.
Seattle University · USRice University · USSaint Louis University · USUniversity of Washington · 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 MAUREEN E NEITZ · 1985 to 2026
$23.5M
STRUCTURAL NEUROCHEMISTRY OF RETINAL CIRCUITSR01EY002576 · NEI · UNIVERSITY OF UTAH · PI MARC, ROBERT E · 1985 to 2016
$8.0M
VISUAL SCIENCET32EY007125 · NEI · UNIVERSITY OF ROCHESTER · PI Krystel R Huxlin, Duje Tadin · 1990 to 2026
$7.1M
Retinal RemodelingR01EY015128 · NEI · UNIVERSITY OF UTAH · PI JONES, BRYAN WILLIAM · 2004 to 2021
$7.0M
VISUAL SCIENCES TRAINING PROGRAMT32EY007031 · NEI · UNIVERSITY OF WASHINGTON · PI Wyeth Daniel Bair, Anitha Pasupathy · 1985 to 2026
$6.1M
Retinal CircuitryR01EY028927 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Bryan William Jones · 2019 to 2026
$5.2M
Linking retinal circuits to perceptionR01EY027859 · NEI · UNIVERSITY OF WASHINGTON · PI Jay Neitz · 2018 to 2026
$4.4M
Reimbursement request for attending the Meeting of the Jointly Sponsored Institutional Predoctoral Training in the Neurosciences T32 Program Directors in Baltimore, MD on 2/19/19T32NS099578 · NINDS · UNIVERSITY OF WASHINGTON · PI SULLIVAN, JANE M, WONG, RACHEL O · 2016 to 2020
$1.4M
Foveal ganglion cell function in the living eyeF32EY032318 · NEI · UNIVERSITY OF ROCHESTER · PI PATTERSON, SARA S · 2021 to 2022
$153k
REGULATION OF THE OUTER BLOOD-RETINAL BARRIERF32EY007031 · NEI · YALE UNIVERSITY · PI WILT, STEVEN D · 1999 to 2000
$11k
NEI NIH HHS F32 EY007031NEI NIH HHS F32 EY032318NEI NIH HHS P30 EY001730NEI NIH HHS R01 EY002576NEI NIH HHS R01 EY015128NEI NIH HHS R01 EY027859NEI NIH HHS R01 EY028927NEI NIH HHS T32 EY007031NEI NIH HHS T32 EY007125NIH HHS EY027859, EY002576, NS099578, EY007031, EY007125, EY032318, P51-OD010425/ORID and P30-EY001730NIH HHS P51 OD010425NINDS NIH HHS T32 NS099578
6 · The paper itself

Abstract

Ganglion cells are the projection neurons of the retina. Intrinsically photosensitive retinal ganglion cells (ipRGCs) express the photopigment melanopsin and also receive input from rods and cones via bipolar cells and amacrine cells. In primates, multiple types of ipRGCs have been identified. The ipRGCs with somas in the ganglion cell layer have been studied extensively, but less is known about those with somas in the inner nuclear layer, the "displaced" cells. To investigate their synaptic inputs, three sets of horizontal, ultrathin sections through central macaque retina were collected using serial block-face scanning electron microscopy. One displaced ipRGC received nearly all of its excitatory inputs from ON bipolar cells and would therefore be expected to have ON responses to light. In each of the three volumes, there was also at least one cell that had a large soma in the inner nuclear layer, varicose axons and dendrites with a large diameter that formed large, extremely sparse arbor in the outermost stratum of the inner plexiform layer. They were identified as the displaced M1 type of ipRGCs based on this morphology and on the high density of granules in their somas. They received extensive input from amacrine cells, including the dopaminergic type. The vast majority of their excitatory inputs were from OFF bipolar cells, including two subtypes with extensive input from the primary rod pathway. They would be expected to have OFF responses to light stimuli below the threshold for melanopsin or soon after the offset of a light stimulus.

Indexed as

MacacaRetinaAmacrine CellsAnimalsGangliaRetinal Ganglion Cells

Identifiers

PMID36071126
PMCPMC9452553
OpenAlexW4294990731

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.