Evidence map›Paper›PMID 25339867›Full record

ArticleFrontiers in neural circuits2014

Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal.

Johana Trojanova, Akos Kulik, Jiri Janacek, Michaela Kralikova, Josef Syka, Rostislav Turecek

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neural circuits, 2014. 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
0.3field-weighted citation impact, top 50% 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, 8 citations in OpenAlex.

  1. Article
  2. The role of GABAFrontiers in endocrinology · 2023
    Review
  3. Review
  4. Article
  5. Editorial: Inhibitory function in auditory processing.Frontiers in neural circuits · 2015
    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

6 authors at 3 institutions in 2 countries.

Johana TrojanovaDepartment of Auditory Neuroscience, Laboratory of Synaptic Transmission, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic Prague, Czech Republic.
Akos KulikDepartment of Physiology II, University of Freiburg Freiburg, Germany ; BIOSS Centre for Biological Signalling Studies, University of Freiburg Freiburg, Germany.
Jiri JanacekDepartment of Biomathematics, Institute of Physiology, Academy of Sciences of the Czech Republic Prague, Czech Republic.
Michaela KralikovaDepartment of Auditory Neuroscience, Laboratory of Synaptic Transmission, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic Prague, Czech Republic.
Josef SykaDepartment of Auditory Neuroscience, Laboratory of Synaptic Transmission, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic Prague, Czech Republic.
Rostislav TurecekDepartment of Auditory Neuroscience, Laboratory of Synaptic Transmission, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic Prague, Czech Republic.
Czech Academy of Sciences, Institute of Experimental Medicine · CZCzech Academy of Sciences · CZUniversity of Freiburg · DE

Funding

Wellcome Trust
6 · The paper itself

Abstract

The physiological functions of glycine receptors (GlyRs) depend on their subcellular locations. In axonal terminals of the central neurons, GlyRs trigger a slow facilitation of presynaptic transmitter release; however, their spatial relationship to the release sites is not known. In this study, we examined the distribution of GlyRs in the rat glutamatergic calyx of Held nerve terminal using high-resolution pre-embedding immunoelectron microscopy. We performed a quantitative analysis of GlyR-associated immunogold (IG) labeling in 3D reconstructed calyceal segments. A variable density of IG particles and their putative accumulations, inferred from the frequency distribution of inter-IG distances, indicated a non-uniform distribution of the receptors in the calyx. Subsequently, increased densities of IG particles were found in calyceal swellings, structures characterized by extensive exocytosis of glutamate. In swellings as well as in larger calyceal stalks, IG particles did not tend to accumulate near the glutamate releasing zones. On the other hand, GlyRs in swellings (but not in stalks) preferentially occupied membrane regions, unconnected to postsynaptic cells and presumably accessible by ambient glycine. Furthermore, the sites with increased GlyR concentrations were found in swellings tightly juxtaposed with GABA/glycinergic nerve endings. Thus, the results support the concept of an indirect mechanism underlying the modulatory effects of calyceal GlyRs, activated by glycine spillover. We also suggest the existence of an activity-dependent mechanism regulating the surface distribution of α homomeric GlyRs in axonal terminals of central neurons.

Indexed as

AnimalsBrain Stemgamma-Aminobutyric AcidGlycineIn Vitro TechniquesMaleNeuronsPresynaptic TerminalsRatsRats, WistarReceptors, GlycineStatistics, NonparametricSynapsesVesicular Glutamate Transport Protein 1gamma-Aminobutyric AcidGlycineReceptors, GlycineVesicular Glutamate Transport Protein 1calyx of Heldglycine receptorMNTBpre-embedding immunoelectron microscopypresynapticspillover

Identifiers

PMID25339867
PMCPMC4186306
OpenAlexW1982236208

What OpenQuestion holds

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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.