Evidence map›Paper›PMID 20807794›Full record

ArticleThe Journal of physiology2010

Fast glutamate uptake via EAAT2 shapes the cone-mediated light offset response in bipolar cells.

Matthew J M Rowan, Harris Ripps, Wen Shen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Contribution of pannexin channels to afterimage signals in the amphibian retina.American journal of physiology. Cell physiology · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Contributions of glutamate transporters and CaExperimental eye research · 2019
    Article
  8. CaeLife · 2019
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  13. Rapid synaptic vesicle endocytosis in cone photoreceptors of salamander retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  14. The mode of retinal presynaptic inhibition switches with light intensity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  15. Glutamate spillover between mammalian cone photoreceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  16. Article
  17. 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 2 institutions in 1 country.

Matthew J M RowanDepatment of Basic Science, Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL 33431, USA.
Harris Ripps
Wen Shen
Florida Atlantic University · USMarine Biological Laboratory · US

Funding

Interplexiform Cell FunctionR01EY014161 · NEI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHEN, WEN · 2002 to 2005
$1.1M
NEI NIH HHS EY 14161NEI NIH HHS R01 EY014161
6 · The paper itself

Abstract

Excitatory amino acid transporters (EAATs) are responsible for extracellular glutamate uptake within the retina, and are expressed by retinal neurons and Müller cells. Their role within glutamatergic synapses is not completely understood. In the salamander retina, five distinct EAAT-encoding genes have been cloned, making the amphibian retina an excellent system to study EAAT function. This study focused on sEAAT2, which is expressed in photoreceptor terminals and Off-bipolar cells in two isoforms, sEAAT2A and sEAAT2B. Using whole-cell patch-clamp recording, florescence imaging and antibody labelling methods, we systematically studied the functions of these two isoforms at the synapse between photoreceptors and bipolar cells, both in dark and with photic stimulation. Both sEAAT2A and sEAAT2B were sensitive to dihydrokainic acid (DHKA), a known EAAT2-specific inhibitor. Each isoform of sEAAT2 was found to play a role in tonic glutamate uptake at the cone synapse in darkness. Furthermore, presynaptic sEAAT2A strongly suppressed the rapid, transient glutamate signal from cones following light-offset. This was achieved by quickly binding exocytosed glutamate, which subsequently limited glutamate spillover to adjacent receptors at postsynaptic sites. Since the intensity and duration of photic stimulation determine the magnitude of these cone transient signals, we postulate that presynaptic cone EAATs contribute to the encoding of contrast sensitivity in cone vision.

Indexed as

AnimalsCaudataExcitatory Amino Acid Transporter 2Glutamic AcidImmunohistochemistryLightPatch-Clamp TechniquesPhotic StimulationRetinal Bipolar CellsRetinal Cone Photoreceptor CellsSynapsesSynaptic TransmissionVision, OcularExcitatory Amino Acid Transporter 2Glutamic Acid

Identifiers

PMID20807794
PMCPMC3000584
OpenAlexW2154928340

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.