Evidence map›Paper›PMID 26728568›Full record

ArticleMolecular psychiatry2016

A critical role for VEGF and VEGFR2 in NMDA receptor synaptic function and fear-related behavior.

P De Rossi, E Harde, J P Dupuis, L Martin, N Chounlamountri, M Bardin, C Watrin, C Benetollo, K Pernet-Gallay, H J Luhmann and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2016. 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
3.7field-weighted citation impact, top 7% 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, 89 citations in OpenAlex.

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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

16 authors at 7 institutions in 3 countries.

P De RossiInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
E HardeInstitute of Cell Biology and Neuroscience and BMLS, Goethe University Frankfurt, Frankfurt, Germany.
J P DupuisInterdisciplinary Institute for Neuroscience, Unité Mixte de Recherche 5297, Université de Bordeaux, Bordeaux, France.
L MartinInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
N ChounlamountriInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
M BardinInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
C WatrinInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
C BenetolloInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
K Pernet-GallayGrenoble Institute of Neurosciences, Grenoble, France.
H J LuhmannInstitute of Physiology, University Medical Center, University of Mainz, Mainz, Germany.
J HonnoratInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
G MalleretInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
L GrocInterdisciplinary Institute for Neuroscience, Unité Mixte de Recherche 5297, Université de Bordeaux, Bordeaux, France.
A Acker-PalmerInstitute of Cell Biology and Neuroscience and BMLS, Goethe University Frankfurt, Frankfurt, Germany.
P A SalinInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
C MeissirelInstitut National de la Santé et de la Recherche Médicale, Unité 1028, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5292, Lyon, France.
Université Claude Bernard Lyon 1 · FRCentre de Recherche en Neurosciences de Lyon · FRInserm · FRInstitut Interdisciplinaire de Neuroscience · FRJohannes Gutenberg University Mainz · DEMax Planck Institute for Brain Research · DENeurophysiologie et nouvelles microscopies · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular endothelial growth factor (VEGF) is known to be required for the action of antidepressant therapies but its impact on brain synaptic function is poorly characterized. Using a combination of electrophysiological, single-molecule imaging and conditional transgenic approaches, we identified the molecular basis of the VEGF effect on synaptic transmission and plasticity. VEGF increases the postsynaptic responses mediated by the N-methyl-D-aspartate type of glutamate receptors (GluNRs) in hippocampal neurons. This is concurrent with the formation of new synapses and with the synaptic recruitment of GluNR expressing the GluN2B subunit (GluNR-2B). VEGF induces a rapid redistribution of GluNR-2B at synaptic sites by increasing the surface dynamics of these receptors within the membrane. Consistently, silencing the expression of the VEGF receptor 2 (VEGFR2) in neural cells impairs hippocampal-dependent synaptic plasticity and consolidation of emotional memory. These findings demonstrated the direct implication of VEGF signaling in neurons via VEGFR2 in proper synaptic function. They highlight the potential of VEGF as a key regulator of GluNR synaptic function and suggest a role for VEGF in new therapeutic approaches targeting GluNR in depression.

Indexed as

AnimalsBehavior, AnimalCell Culture TechniquesExcitatory Postsynaptic PotentialsFearHippocampusMiceNeuronal PlasticityNeuronsProtein SubunitsReceptors, GlutamateReceptors, N-Methyl-D-AspartateSynapsesSynaptic TransmissionVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Kdr protein, mouseProtein SubunitsReceptors, GlutamateReceptors, N-Methyl-D-AspartateVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID26728568
PMCPMC5116482
OpenAlexW2231740780

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.