Evidence map›Paper›PMID 33154448›Full record

ArticleScientific reports2020

3-O-sulfated heparan sulfate interactors target synaptic adhesion molecules from neonatal mouse brain and inhibit neural activity and synaptogenesis in vitro.

Auriane Maïza, Nazha Sidahmed-Adrar, Patrick P Michel, Gilles Carpentier, Damien Habert, Carine Dalle, Walid Redouane, Magda Hamza, T H van Kuppevelt, Mohand Ouidir Ouidja and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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
1.1field-weighted citation impact, top 25% 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.

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  8. Review
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  10. Synthesis of 3-ACS chemical biology · 2021
    Article
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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

14 authors at 5 institutions in 3 countries.

Auriane MaïzaGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Nazha Sidahmed-AdrarGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Patrick P MichelParis Brain Institute, CNRS UMR 7225, INSERM U 1127, Sorbonne Université, Paris, France.
Gilles CarpentierGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Damien HabertGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Carine DalleParis Brain Institute, CNRS UMR 7225, INSERM U 1127, Sorbonne Université, Paris, France.
Walid RedouaneGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Magda HamzaGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
T H van KuppeveltDepartment of Biochemistry, Radboud University Medical Centre, Nijmegen, The Netherlands.
Mohand Ouidir OuidjaGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
José CourtyGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Sandrine ChantepieGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Dulce Papy-GarciaGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France.
Olivier StettlerGly-CRRET-Croissance Cellulaire, Réparation et Régénération Tissulaire, Univ Paris Est Creteil, Gly-CRRET, F-94010, Creteil, France. olivier.stettler@u-pec.fr.
Université Paris-Est Créteil · FRLaboratoire de Recherche sur la Croissance Cellulaire, la Réparation et la Régénération Tissulaires · FRAllen Institute for Brain Science · USCentre National de la Recherche Scientifique · FRRadboud University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heparan sulfate (HS) chains, covalently linked to heparan sulfate proteoglycans (HSPG), promote synaptic development and functions by connecting various synaptic adhesion proteins (AP). HS binding to AP could vary according to modifications of HS chains by different sulfotransferases. 3-O-sulfotransferases (Hs3sts) produce rare 3-O-sulfated HSs (3S-HSs), of poorly known functions in the nervous system. Here, we showed that a peptide known to block herpes simplex virus by interfering with 3S-HSs in vitro and in vivo (i.e. G2 peptide), specifically inhibited neural activity, reduced evoked glutamate release, and impaired synaptic assembly in hippocampal cell cultures. A role for 3S-HSs in promoting synaptic assembly and neural activity is consistent with the synaptic interactome of G2 peptide, and with the detection of Hs3sts and their products in synapses of cultured neurons and in synaptosomes prepared from developing brains. Our study suggests that 3S-HSs acting as receptors for herpesviruses might be important regulators of neuronal and synaptic development in vertebrates.

Indexed as

AnimalsCells, CulturedHeparan SulfateHeparan Sulfate ProteoglycansHippocampusMiceNeurogenesisNeuronsSulfotransferasesSynapsesHeparan SulfateHeparan Sulfate ProteoglycansSulfotransferases

Identifiers

PMID33154448
PMCPMC7644699
OpenAlexW3097933625

What Socratic 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 Socratic graph.