Evidence map›Paper›PMID 35532105›Full record

ArticleeLife2022

MDGAs are fast-diffusing molecules that delay excitatory synapse development by altering neuroligin behavior.

Andrea Toledo, Mathieu Letellier, Giorgia Bimbi, Béatrice Tessier, Sophie Daburon, Alexandre Favereaux, Ingrid Chamma, Kristel Vennekens, Jeroen Vanderlinden, Matthieu Sainlos and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  3. Localization and Functional Characterization of MDGA1 in Mouse Hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  7. microRNA-218-5p coordinates scaling of excitatory and inhibitory synapses during homeostatic synaptic plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  14. MDGAs perform activity-dependent synapse type-specific suppression via distinct extracellular mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

13 authors at 2 institutions in 2 countries.

Andrea ToledoUniversity of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.
Mathieu Letellier *University of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.ORCID 0000-0003-4008-298X
Giorgia Bimbi *University of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.
Béatrice TessierUniversity of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.
Sophie DaburonUniversity of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.
Alexandre FavereauxUniversity of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.
Ingrid ChammaUniversity of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.
Kristel VennekensVIB Center for Brain & Disease Research and KU Leuven, Department of Neurosciences, Leuven Brain Institute, Leuven, Belgium.
Jeroen VanderlindenVIB Center for Brain & Disease Research and KU Leuven, Department of Neurosciences, Leuven Brain Institute, Leuven, Belgium.
Matthieu SainlosUniversity of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.ORCID 0000-0001-5465-5641
Joris de WitVIB Center for Brain & Disease Research and KU Leuven, Department of Neurosciences, Leuven Brain Institute, Leuven, Belgium.
Daniel Choquet *University of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.
Olivier Thoumine *University of Bordeaux, CNRS UMR 5297, Interdisciplinary Institute for Neuroscience, Bordeaux, France.ORCID 0000-0002-8041-1349
Centre National de la Recherche Scientifique · FRVIB-KU Leuven Center for Brain & Disease Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MDGA molecules can bind neuroligins and interfere with trans-synaptic interactions to neurexins, thereby impairing synapse development. However, the subcellular localization and dynamics of MDGAs, or their specific action mode in neurons remain unclear. Here, surface immunostaining of endogenous MDGAs and single molecule tracking of recombinant MDGAs in dissociated hippocampal neurons reveal that MDGAs are homogeneously distributed and exhibit fast membrane diffusion, with a small reduction in mobility across neuronal maturation. Knocking-down/out MDGAs using shRNAs and CRISPR/Cas9 strategies increases the density of excitatory synapses, the membrane confinement of neuroligin-1, and the phosphotyrosine level of neuroligins associated with excitatory post-synaptic differentiation. Finally, MDGA silencing reduces the mobility of AMPA receptors, increases the frequency of miniature EPSCs (but not IPSCs), and selectively enhances evoked AMPA-receptor-mediated EPSCs in CA1 pyramidal neurons. Overall, our results support a mechanism by which interactions between MDGAs and neuroligin-1 delays the assembly of functional excitatory synapses containing AMPA receptors.

Indexed as

Nerve Tissue ProteinsReceptors, AMPACell Adhesion Molecules, NeuronalHippocampusNeuronsSynapsesCell Adhesion Molecules, NeuronalNerve Tissue ProteinsReceptors, AMPAadhesion moleculescell biologyElectrophysiologyhippocampal culturesneuroscienceratsingle molecule trackingsynapse development

Identifiers

PMID35532105
PMCPMC9084894
OpenAlexW4229003996

What OpenQuestion holds

Textmetadata
LicenceCC0
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.