Evidence map›Paper›PMID 34878402›Full record

ArticleeLife2021

Identification of a stereotypic molecular arrangement of endogenous glycine receptors at spinal cord synapses.

Stephanie A Maynard, Philippe Rostaing, Natascha Schaefer, Olivier Gemin, Adrien Candat, Andréa Dumoulin, Carmen Villmann, Antoine Triller, Christian G Specht

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Competition between glycine and GABAProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Role of the Glycine Receptor β Subunit in Synaptic Localization and Pathogenicity in Severe Startle Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  8. Startle Disease: New Molecular Insights into an Old Neurological Disorder.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
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

9 authors at 2 institutions in 2 countries.

Stephanie A MaynardInstitut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, Inserm, PSL University, Paris, France.ORCID https://orcid.org/0000-0002-7838-3676
Philippe RostaingInstitut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, Inserm, PSL University, Paris, France.
Natascha SchaeferInstitute for Clinical Neurobiology, University Hospital, Julius-Maximilians-University, Wuerzburg, Germany.ORCID https://orcid.org/0000-0001-9743-1963
Olivier GeminInstitut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, Inserm, PSL University, Paris, France.ORCID https://orcid.org/0000-0003-3210-7876
Adrien CandatInstitut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, Inserm, PSL University, Paris, France.
Andréa DumoulinInstitut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, Inserm, PSL University, Paris, France.
Carmen VillmannInstitute for Clinical Neurobiology, University Hospital, Julius-Maximilians-University, Wuerzburg, Germany.ORCID https://orcid.org/0000-0003-1498-6950
Antoine TrillerInstitut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, Inserm, PSL University, Paris, France.ORCID https://orcid.org/0000-0002-7530-1233
Christian G SpechtInstitut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, Inserm, PSL University, Paris, France.ORCID https://orcid.org/0000-0001-6038-7735
Inserm · FRUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise quantitative information about the molecular architecture of synapses is essential to understanding the functional specificity and downstream signaling processes at specific populations of synapses. Glycine receptors (GlyRs) are the primary fast inhibitory neurotransmitter receptors in the spinal cord and brainstem. These inhibitory glycinergic networks crucially regulate motor and sensory processes. Thus far, the nanoscale organization of GlyRs underlying the different network specificities has not been defined. Here, we have quantitatively characterized the molecular arrangement and ultra-structure of glycinergic synapses in spinal cord tissue using quantitative super-resolution correlative light and electron microscopy. We show that endogenous GlyRs exhibit equal receptor-scaffold occupancy and constant packing densities of about 2000 GlyRs µm

Indexed as

AnimalsMiceMolecular StructureReceptors, GlycineSpinal CordSynapsesReceptors, Glycinecorrelative light and electron microscopyelectron microscopyglycine receptorhyperekplexiamouseneuroscienceoscillator mouse modelsingle molecule localization microscopyspinal cord

Identifiers

PMID34878402
PMCPMC8752092
OpenAlexW4226039686

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.