Evidence map›Paper›PMID 35658004›Full record

ArticlePLoS biology2022

Alix is required for activity-dependent bulk endocytosis at brain synapses.

Marine H Laporte, Kwang Il Chi, Laura C Caudal, Na Zhao, Yvonne Schwarz, Marta Rolland, José Martinez-Hernandez, Magalie Martineau, Christine Chatellard, Eric Denarier and 12 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  5. The epithelial NaCell reports · 2023
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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

22 authors at 4 institutions in 5 countries.

Marine H LaporteGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.ORCID 0000-0002-7856-6763
Kwang Il ChiGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.ORCID 0000-0002-9402-661X
Laura C CaudalMolecular Physiology, Center for Integrative Physiology and Molecular Medicine (CIPMM), University of Saarland, Homburg, Germany.ORCID 0000-0003-2165-281X
Na ZhaoMolecular Physiology, Center for Integrative Physiology and Molecular Medicine (CIPMM), University of Saarland, Homburg, Germany.ORCID 0000-0003-1780-7700
Yvonne SchwarzMolecular Neurophysiology, Center for Integrative Physiology and Molecular Medicine (CIPMM), University of Saarland, Homburg, Germany.
Marta RollandGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
José Martinez-HernandezGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.ORCID 0000-0002-5017-2877
Magalie MartineauInterdisciplinary Institute for Neuroscience, University of Bordeaux-CNRS UMR 5297, Bordeaux, France.
Christine ChatellardGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.ORCID 0000-0002-4962-9884
Eric DenarierGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.ORCID 0000-0002-4169-397X
Vincent MercierGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
Florent LemaîtreGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
Béatrice BlotGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.ORCID 0000-0002-6279-5764
Eve MoutauxGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
Maxime CazorlaGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
David PerraisInterdisciplinary Institute for Neuroscience, University of Bordeaux-CNRS UMR 5297, Bordeaux, France.
Fabien LantéGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
Dieter BrunsMolecular Neurophysiology, Center for Integrative Physiology and Molecular Medicine (CIPMM), University of Saarland, Homburg, Germany.
Sandrine FrabouletGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
Fiona J HemmingGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
Frank KirchhoffMolecular Physiology, Center for Integrative Physiology and Molecular Medicine (CIPMM), University of Saarland, Homburg, Germany.ORCID 0000-0002-2324-2761
Rémy SadoulGrenoble Institute Neurosciences, University Grenoble Alpes-INSERM U1216-CEA, Grenoble, France.
Inserm · FRCentre National de la Recherche Scientifique · FRSaarland University · DEUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In chemical synapses undergoing high frequency stimulation, vesicle components can be retrieved from the plasma membrane via a clathrin-independent process called activity-dependent bulk endocytosis (ADBE). Alix (ALG-2-interacting protein X/PDCD6IP) is an adaptor protein binding to ESCRT and endophilin-A proteins which is required for clathrin-independent endocytosis in fibroblasts. Alix is expressed in neurons and concentrates at synapses during epileptic seizures. Here, we used cultured neurons to show that Alix is recruited to presynapses where it interacts with and concentrates endophilin-A during conditions triggering ADBE. Using Alix knockout (ko) neurons, we showed that this recruitment, which requires interaction with the calcium-binding protein ALG-2, is necessary for ADBE. We also found that presynaptic compartments of Alix ko hippocampi display subtle morphological defects compatible with flawed synaptic activity and plasticity detected electrophysiologically. Furthermore, mice lacking Alix in the forebrain undergo less seizures during kainate-induced status epilepticus and reduced propagation of the epileptiform activity. These results thus show that impairment of ADBE due to the lack of neuronal Alix leads to abnormal synaptic recovery during physiological or pathological repeated stimulations.

Indexed as

EndocytosisSynapsesAnimalsBrainCalcium-Binding ProteinsClathrinMiceNeuronsCalcium-Binding ProteinsClathrinPdcd6ip protein, mouse

Identifiers

PMID35658004
PMCPMC9200306
OpenAlexW4281670932

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.