Evidence map›Paper›PMID 19052203›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2008

Unique luminal localization of VGAT-C terminus allows for selective labeling of active cortical GABAergic synapses.

Henrik Martens, Matthew C Weston, Jean-Luc Boulland, Mads Grønborg, Jens Grosche, Johannes Kacza, Anke Hoffmann, Michela Matteoli, Shigeo Takamori, Tibor Harkany and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

48 citing papers in PubMed, 90 citations in OpenAlex.

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  8. Spontaneously Recycling Synaptic Vesicles Constitute Readily Releasable Vesicles in Intact Neuromuscular Synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  9. Association ofNeurology · 2021
    Article
  10. Review
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  19. Positive Allosteric Modulation as a Potential Therapeutic Strategy in Anti-NMDA Receptor Encephalitis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  20. Review
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

15 authors at 8 institutions in 7 countries.

Henrik MartensSynaptic Systems GmbH, Göttingen, Germany. lab@sysy.com
Matthew C Weston
Jean-Luc Boulland
Mads Grønborg
Jens Grosche
Johannes Kacza
Anke Hoffmann
Michela Matteoli
Shigeo Takamori
Tibor Harkany
Farrukh A Chaudhry
Christian Rosenmund
Christian Erck
Reinhard Jahn
Wolfgang Härtig
Leipzig University · DEBaylor College of Medicine · USMax Planck Institute for Biophysical Chemistry · DESynaptic Research (United States) · USUniversity of Oslo · NOKnowledge Integration (United Kingdom) · GBUniversity of Aberdeen · GBUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurotransmitter uptake into synaptic vesicles is mediated by vesicular neurotransmitter transporters. Although these transporters belong to different families, they all are thought to share a common overall topology with an even number of transmembrane domains. Using epitope-specific antibodies and mass spectrometry we show that the vesicular GABA transporter (VGAT) possesses an uneven number of transmembrane domains, with the N terminus facing the cytoplasm and the C terminus residing in the synaptic vesicle lumen. Antibodies recognizing the C terminus of VGAT (anti-VGAT-C) selectively label GABAergic nerve terminals of live cultured hippocampal and striatal neurons as confirmed by immunocytochemistry and patch-clamp electrophysiology. Injection of fluorochromated anti-VGAT-C into the hippocampus of mice results in specific labeling of GABAergic synapses in vivo. Overall, our data open the possibility of studying novel GABA release sites, characterizing inhibitory vesicle trafficking, and establishing their contribution to inhibitory neurotransmission at identified GABAergic synapses.

Indexed as

AnimalsAntibody SpecificityCorpus StriatumEndocytosisExocytosisgamma-Aminobutyric AcidHippocampusImmunohistochemistryMass SpectrometryMiceNeural InhibitionPatch-Clamp TechniquesProsencephalonProtein Structure, TertiaryStaining and LabelingSynapsesgamma-Aminobutyric Acidvesicular GABA transporterVesicular Inhibitory Amino Acid Transport Proteins

Identifiers

PMID19052203
PMCPMC6671625
OpenAlexW1995510156

What OpenQuestion holds

Textmetadata
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.