Evidence map›Paper›PMID 24760782›Full record

ArticleJournal of neurophysiology2014

Evidence of calcium-permeable AMPA receptors in dendritic spines of CA1 pyramidal neurons.

Hayley A Mattison, Ashish A Bagal, Michael Mohammadi, Nisha S Pulimood, Christian G Reich, Bradley E Alger, Joseph P Y Kao, Scott M Thompson

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  5. Review
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  8. Review
  9. Review
  10. Article
  11. Auxiliary Subunit GSG1L Acts to Suppress Calcium-Permeable AMPA Receptor Function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  12. 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

8 authors at 1 institution in 1 country.

Hayley A MattisonDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland; Membrane Biology Training Program, University of Maryland School of Medicine, Baltimore, Maryland;
Ashish A BagalDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland;
Michael MohammadiDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland;
Nisha S PulimoodDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland; Program in Neuroscience, University of Maryland School of Medicine, Baltimore, Maryland; and.
Christian G ReichDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland;
Bradley E AlgerDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland; Membrane Biology Training Program, University of Maryland School of Medicine, Baltimore, Maryland;
Joseph P Y KaoDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland; Membrane Biology Training Program, University of Maryland School of Medicine, Baltimore, Maryland; Center for Biomedical Engineering and Technology, University of Maryland School of Medicine, Baltimore, Maryland.
Scott M ThompsonDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland; Membrane Biology Training Program, University of Maryland School of Medicine, Baltimore, Maryland; sthom003@umaryland.edu.
University of Maryland, Baltimore · US

Funding

TRAINING PROGRAM IN INTEGRATIVE MEMBRANE BIOLOGYT32GM008181 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI RIZZO, MEGAN A, TRUDEAU, MATTHEW C · 1987 to 2022
$4.9M
Stress, Depression, Serotonin, and Plasticity of Excitatory TransmissionR01MH086828 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI THOMPSON, SCOTT M. · 2010 to 2019
$3.8M
CAGED PROBES FOR CELLULAR PHYSIOLOGYR01GM056481 · NIGMS · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI KAO, JOSEPH PAO YUNG · 1998 to 2009
$3.3M
Endocannabinoids and GABAergic Control of PlasticityR01DA014625 · NIDA · UNIVERSITY OF MARYLAND BALTIMORE · PI ALGER, BRADLEY E · 2001 to 2011
$2.9M
Interactions Among Hippocampal Interneuron CircuitsR01MH077277 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI ALGER, BRADLEY E · 2006 to 2012
$1.8M
Plasticity of Hippocampal Structure and FunctionR01MH065488 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI THOMPSON, SCOTT M. · 2002 to 2006
$1.5M
The Role of Glutamate in the Physiological Development of Dendritic SpinesF31MH079668 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI MATTISON, HAYLEY A · 2007 to 2009
$77k
NIDA NIH HHS R01-DA-014625NIGMS NIH HHS R01-GM-056481NIGMS NIH HHS T32 GM008181NIMH NIH HHS F31 MH079668NIMH NIH HHS F31-MH-079668NIMH NIH HHS R01 MH065488NIMH NIH HHS R01-MH-077277NIMH NIH HHS R01 MH086828NIMH NIH HHS R01-MH-086828NIMH NIH HHS R01-MH-65488
6 · The paper itself

Abstract

GluA2-lacking, calcium-permeable α-amino-3-hydroxy-5-methylisoxazole-4-propionate receptors (AMPARs) have unique properties, but their presence at excitatory synapses in pyramidal cells is controversial. We have tested certain predictions of the model that such receptors are present in CA1 cells and show here that the polyamine spermine, but not philanthotoxin, causes use-dependent inhibition of synaptically evoked excitatory responses in stratum radiatum, but not s. oriens, in cultured and acute hippocampal slices. Stimulation of single dendritic spines by photolytic release of caged glutamate induced an N-methyl-d-aspartate receptor-independent, use- and spermine-sensitive calcium influx only at apical spines in cultured slices. Bath application of glutamate also triggered a spermine-sensitive influx of cobalt into CA1 cell dendrites in s. radiatum. Responses of single apical, but not basal, spines to photostimulation displayed prominent paired-pulse facilitation (PPF) consistent with use-dependent relief of cytoplasmic polyamine block. Responses at apical dendrites were diminished, and PPF was increased, by spermine. Intracellular application of pep2m, which inhibits recycling of GluA2-containing AMPARs, reduced apical spine responses and increased PPF. We conclude that some calcium-permeable, polyamine-sensitive AMPARs, perhaps lacking GluA2 subunits, are present at synapses on apical dendrites of CA1 pyramidal cells, which may allow distinct forms of synaptic plasticity and computation at different sets of excitatory inputs.

Indexed as

AnimalsCA1 Region, HippocampalCalciumCobaltDendritic SpinesExcitatory Postsynaptic PotentialsGlutamic AcidMalePolyaminesPyramidal CellsRatsRats, Sprague-DawleyReceptors, AMPASpermineSynapsesCalciumCobaltdelta-philanthotoxinGlutamic AcidPolyaminesReceptors, AMPASperminecalciumglutamatehippocampuspolyaminessynaptic transmission

Identifiers

PMID24760782
PMCPMC4064414
OpenAlexW2041502078

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.