Evidence map›Paper›PMID 36223749›Full record

ArticleCell reports2022

Calcium-permeable AMPA receptors on AII amacrine cells mediate sustained signaling in the On-pathway of the primate retina.

Kumiko A Percival, Jacqueline Gayet, Roupen Khanjian, W Rowland Taylor, Teresa Puthussery

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Kumiko A PercivalCasey Eye Institute, Oregon Health & Science University, Portland, OR 97239, USA.
Jacqueline GayetHerbert Wertheim School of Optometry & Vision Science, University of California, Berkeley, Berkeley, CA 94720-2020, USA.
Roupen KhanjianCasey Eye Institute, Oregon Health & Science University, Portland, OR 97239, USA.
W Rowland TaylorHerbert Wertheim School of Optometry & Vision Science, University of California, Berkeley, Berkeley, CA 94720-2020, USA; Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720-2020, USA.
Teresa PuthusseryHerbert Wertheim School of Optometry & Vision Science, University of California, Berkeley, Berkeley, CA 94720-2020, USA; Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720-2020, USA. Electronic address: tputhussery@berkeley.edu.
University of California, Berkeley · USOregon Health & Science University · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
YR 50 PROJ- ROBERTS PRIMATE ISLETP51RR000163 · NCRR · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI PICKER, LOUIS J. · 1985 to 2011
$140.8M
UC Berkeley Vision Science COREP30EY003176 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI RICHARD H KRAMER · 1985 to 2026
$16.4M
Mechanisms of Synaptic Processing in the RetinaR01EY014888 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TAYLOR, WILLIAM ROWLAND · 2003 to 2015
$4.4M
Structure and Function of Primate Retinal CircuitsR01EY024265 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI PUTHUSSERY, TERESA · 2014 to 2025
$4.4M
NCRR NIH HHS P51 RR000163NEI NIH HHS P30 EY003176NEI NIH HHS R01 EY014888NEI NIH HHS R01 EY024265NIH HHS P51 OD011092NIH HHS P51 OD011107
6 · The paper itself

Abstract

Midget and parasol ganglion cells (GCs) represent the major output channels from the primate eye to the brain. On-type midget and parasol GCs exhibit a higher background spike rate and thus can respond more linearly to contrast changes than their Off-type counterparts. Here, we show that a calcium-permeable AMPA receptor (CP-AMPAR) antagonist blocks background spiking and sustained light-evoked firing in On-type GCs while preserving transient light responses. These effects are selective for On-GCs and are occluded by a gap-junction blocker suggesting involvement of AII amacrine cells (AII-ACs). Direct recordings from AII-ACs, cobalt uptake experiments, and analyses of transcriptomic data confirm that CP-AMPARs are expressed by primate AII-ACs. Overall, our data demonstrate that under some background light levels, CP-AMPARs at the rod bipolar to AII-AC synapse drive sustained signaling in On-type GCs and thus contribute to the more linear contrast signaling of the primate On- versus Off-pathway.

Indexed as

Amacrine CellsReceptors, AMPAAnimalsCalciumCobaltPrimatesReceptors, Calcium-SensingRetinaCalciumCobaltReceptors, AMPAReceptors, Calcium-SensingCP: NeuroscienceelectrophysiologyIEM1460macaquemagnocellularmidgetparasolparvocellularretinal ganglion cell

Identifiers

PMID36223749
PMCPMC10518213
OpenAlexW4304196304

What OpenQuestion holds

Textmetadata
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.