Evidence map›Paper›PMID 27707974›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Glutamate Clearance Is Locally Modulated by Presynaptic Neuronal Activity in the Cerebral Cortex.

Moritz Armbruster, Elizabeth Hanson, Chris G Dulla

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 2% 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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 135 citations in OpenAlex.

  1. Pooled it
  2. Review
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  11. GluN3A and Excitatory Glycine Receptors in the Adult Hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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  16. Deficits in integrative NMDA receptors caused by Grin1 disruption can be rescued in adulthood.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  17. Review
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10 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Moritz ArmbrusterDepartment of Neuroscience, Tufts University School of Medicine, Boston, Massachusetts 02111, and.
Elizabeth HansonDepartment of Neuroscience, Tufts University School of Medicine, Boston, Massachusetts 02111, and Neuroscience Program, Tufts Sackler School of Biomedical Sciences, Boston, Massachusetts 02111.ORCID 0000-0002-5150-8926
Chris G DullaDepartment of Neuroscience, Tufts University School of Medicine, Boston, Massachusetts 02111, and Neuroscience Program, Tufts Sackler School of Biomedical Sciences, Boston, Massachusetts 02111 Chris.Dulla@Tufts.edu.ORCID 0000-0002-6560-6535
Tufts University · US

Funding

TUSM/T-NEMC CENTER FOR NEUROSCIENCE RESEARCH - Imaging CoreP30NS047243 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2003 to 2017
$10.0M
Impact of Astrocytic Glutamate Transport on Epilepsy Associated with DevelopmentaR01NS076885 · NINDS · TUFTS UNIVERSITY BOSTON · PI DULLA, CHRIS G · 2012 to 2016
$1.8M
Synapse Neurobiology Training ProgramT32NS061764 · NINDS · TUFTS UNIVERSITY BOSTON · PI BIEDERER, THOMAS · 2009 to 2019
$1.7M
The Role of Glutamate Signaling in Developmental Cortical MalformationsR56NS076885 · NINDS · TUFTS UNIVERSITY BOSTON · PI DULLA, CHRIS G · 2017 to 2017
$491k
NINDS NIH HHS P30 NS047243NINDS NIH HHS R01 NS076885NINDS NIH HHS R56 NS076885NINDS NIH HHS T32 NS061764
6 · The paper itself

Abstract

Excitatory amino acid transporters (EAATs) are abundantly expressed by astrocytes, rapidly remove glutamate from the extracellular environment, and restrict the temporal and spatial extent of glutamate signaling. Studies probing EAAT function suggest that their capacity to remove glutamate is large and does not saturate, even with substantial glutamate challenges. In contrast, we report that neuronal activity rapidly and reversibly modulates EAAT-dependent glutamate transport. To date, no physiological manipulation has shown changes in functional glutamate uptake in a nonpathological state. Using iGluSnFr-based glutamate imaging and electrophysiology in the adult mouse cortex, we show that glutamate uptake is slowed up to threefold following bursts of neuronal activity. The slowing of glutamate uptake depends on the frequency and duration of presynaptic neuronal activity but is independent of the amount of glutamate released. The modulation of glutamate uptake is brief, returning to normal within 50 ms after stimulation ceases. Interestingly, the slowing of glutamate uptake is specific to activated synapses, even within the domain of an individual astrocyte. Activity-induced slowing of glutamate uptake, and the increased persistence of glutamate in the extracellular space, is reflected by increased decay times of neuronal NR2A-mediated NMDA currents. These results show that astrocytic clearance of extracellular glutamate is slowed in a temporally and spatially specific manner following bursts of neuronal activity ≥30 Hz and that these changes affect the neuronal response to released glutamate. This suggests a previously unreported form of neuron-astrocyte interaction. SIGNIFICANCE STATEMENT: We report the first fast, physiological modulation of astrocyte glutamate clearance kinetics. We show that presynaptic activity in the cerebral cortex increases the persistence of glutamate in the extracellular space by slowing its clearance by astrocytes. Because of abundant EAAT expression, glutamate clearance from the extracellular space has been thought to have invariant kinetics. While multiple studies report experimental manipulations resulting in altered EAAT expression, our findings show that astrocytic glutamate uptake is dynamic on a fast time-scale. This shows rapid plasticity of glutamate clearance, which locally modulates synaptic signaling in the cortex. As astrocytic glutamate uptake is a fundamental and essential mechanism for neurotransmission, this work has implications for neurotransmission, extrasynaptic receptor activation, and synaptic plasticity.

Indexed as

AnimalsAstrocytesCerebral CortexElectrophysiological PhenomenaExcitatory Amino Acid Transporter 2FemaleGlutamic AcidIn Vitro TechniquesMaleMiceMice, Inbred C57BLNeuronsReceptors, N-Methyl-D-AspartateReceptors, PresynapticExcitatory Amino Acid Transporter 2Glutamic AcidReceptors, N-Methyl-D-AspartateReceptors, Presynapticactivityastrocytecortexglutamateglutamate uptake

Identifiers

PMID27707974
PMCPMC5050332
OpenAlexW2527796387

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.