Evidence map›Paper›PMID 25064059›Full record

ArticleNeuroscience2014

Localization of excitatory amino acid transporters EAAT1 and EAAT2 in human postmortem cortex: a light and electron microscopic study.

R C Roberts, J K Roche, R E McCullumsmith

Abstract read
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
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  16. Chronic Stress Alters Astrocyte Morphology in Mouse Prefrontal Cortex.The international journal of neuropsychopharmacology · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. The Potential Role of Astrocytes in Parkinson's Disease (PD).Medical sciences (Basel, Switzerland) · 2020
    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

3 authors at 2 institutions in 1 country.

R C RobertsDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL, USA. Electronic address: rcusidor@uab.edu.
J K RocheDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL, USA.
R E McCullumsmithDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address: robert.mccullumsmith@uc.edu.
University of Alabama at Birmingham · USUniversity of Cincinnati Medical Center · US

Funding

Defects of subcellular glutamate transporter localization in schizophreniaR01MH094445 · NIMH · UNIVERSITY OF CINCINNATI · PI MCCULLUMSMITH, ROBERT E · 2011 to 2015
$1.7M
Glutamate Transporter Expression in SchizophreniaK08MH074016 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MCCULLUMSMITH, ROBERT E · 2006 to 2010
$872k
Abnormalities of glutamate transporter localization in schizophreniaR21MH087752 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MCCULLUMSMITH, ROBERT E, ROBERTS, ROSALINDA C · 2011 to 2012
$403k
NIMH NIH HHS K08 MH074016NIMH NIH HHS MH074016NIMH NIH HHS MH087752NIMH NIH HHS MH094445NIMH NIH HHS R01 MH094445NIMH NIH HHS R21 MH087752
6 · The paper itself

Abstract

The process of glutamate release, activity, and reuptake involves the astrocyte, the presynaptic and postsynaptic neurons. Glutamate is released into the synapse and may occupy and activate receptors on both neurons and astrocytes. Glutamate is rapidly removed from the synapse by a family of plasma membrane excitatory amino acid transporters (EAATs), also localized to neurons and astrocytes. The purpose of the present study was to examine EAAT labeling in the postmortem human cortex at the light and electron microscopic (EM) levels. The postmortem prefrontal cortex was processed for EAAT1 and EAAT2 immunohistochemistry. At the light microscopic level, EAAT1 and EAAT2 labeling was found in both gray and white matter. Most cellular labeling was in small cells which were morphologically similar to glia. In addition, EAAT1-labeled neurons were scattered throughout, some of which were pyramidal in shape. At the EM level, EAAT1 and EAAT2 labeling was found in astrocytic soma and processes surrounding capillaries. EAAT labeling was also found in small astrocytic processes adjacent to axon terminals forming asymmetric (glutamatergic) synapses. While EAAT2 labeling was most prevalent in astrocytic processes, EAAT1 labeling was also present in neuronal processes including the soma, axons, and dendritic spines. Expression of EAAT1 protein on neurons may be due to the hypoxia associated with the postmortem interval, and requires further confirmation. The localization of EAATs on the astrocytic plasma membrane and adjacent to excitatory synapses is consistent with the function of facilitating glutamate reuptake and limiting glutamate spillover. Establishment that EAAT1 and EAAT2 can be measured at the EM level in human postmortem tissues will permit testing of hypotheses related to these molecules in diseases lacking analogous animal models.

Indexed as

AdultAgedAnimalsAstrocytesExcitatory Amino Acid Transporter 1Excitatory Amino Acid Transporter 2FemaleGlutamate Plasma Membrane Transport ProteinsHumansMaleMice, KnockoutMicroscopy, ElectronMiddle AgedNeuronsPrefrontal CortexSpecies SpecificityExcitatory Amino Acid Transporter 1Excitatory Amino Acid Transporter 2Glutamate Plasma Membrane Transport ProteinsSLC1A2 protein, humanSLC1A3 protein, humanSlc1a3 protein, mouseastrocytesDABdiaminobenzidineEAATselectron microscopicelectron microscopyEMethanolEtOHexcitatory amino acid transportersglutamate transporterlong-term depressionlong-term potentiationLTDLTPmitochondriaNMDAN-methyl-d-aspartatePBPBSphosphate bufferphosphate-buffered salinePMIpostmortem intervalpostsynaptic densityPSDrERrough endoplasmic reticulumultrastructure

Identifiers

PMID25064059
PMCPMC4164610
OpenAlexW1971043748

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.