Evidence map›Paper›PMID 26223835›Full record

ArticleThe Journal of physiology2015

The extracellular matrix molecule brevican is an integral component of the machinery mediating fast synaptic transmission at the calyx of Held.

Maren Blosa, Mandy Sonntag, Carsten Jäger, Solveig Weigel, Johannes Seeger, Renato Frischknecht, Constanze I Seidenbecher, Russell T Matthews, Thomas Arendt, Rudolf Rübsamen and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.3field-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

47 citing papers in PubMed, 75 citations in OpenAlex.

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  6. Proteomic characterization of atopic dermatitis blood from infancy to adulthood.Journal of the American Academy of Dermatology · 2023
    Observational
  7. Net gain and loss: influence of natural rewards and drugs of abuse on perineuronal nets.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Review
  8. Article
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  10. Review
  11. Article
  12. Article
  13. Extracellular Matrix in Neural Plasticity and Regeneration.Cellular and molecular neurobiology · 2022
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

11 authors at 4 institutions in 2 countries.

Maren BlosaPaul Flechsig Institute for Brain Research, Faculty of Medicine, University of Leipzig, 04103, Leipzig, Germany.
Mandy SonntagPaul Flechsig Institute for Brain Research, Faculty of Medicine, University of Leipzig, 04103, Leipzig, Germany.
Carsten JägerPaul Flechsig Institute for Brain Research, Faculty of Medicine, University of Leipzig, 04103, Leipzig, Germany.
Solveig WeigelPaul Flechsig Institute for Brain Research, Faculty of Medicine, University of Leipzig, 04103, Leipzig, Germany.
Johannes SeegerInstitute of Anatomy, Histology and Embryology, Faculty of Veterinary Medicine, University of Leipzig, 04103, Leipzig, Germany.
Renato FrischknechtLeibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Constanze I SeidenbecherLeibniz Institute for Neurobiology, 39118, Magdeburg, Germany.
Russell T MatthewsDepartment of Neuroscience and Physiology, State University of New York Upstate Medical University, Syracuse, NY, 13210, USA.
Thomas ArendtPaul Flechsig Institute for Brain Research, Faculty of Medicine, University of Leipzig, 04103, Leipzig, Germany.
Rudolf RübsamenInstitute of Biology, Faculty of Biology, Pharmacy and Psychology, University of Leipzig, 04103, Leipzig, Germany.
Markus MorawskiPaul Flechsig Institute for Brain Research, Faculty of Medicine, University of Leipzig, 04103, Leipzig, Germany.
Leipzig University · DELeibniz Institute for Neurobiology · DELeipzig University of Applied Sciences · DESUNY Upstate Medical University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

key pointsThe proteoglycan brevican is a major component of the extracellular matrix of perineuronal nets and is highly enriched in the perisynaptic space suggesting a role for synaptic transmission. We have introduced the calyx of Held in the auditory brainstem as a model system to study the impact of brevican on dynamics and reliability of synaptic transmission. In vivo extracellular single-unit recordings at the calyx of Held in brevican-deficient mice yielded a significant increase in the action potential (AP) transmission delay and a prolongation of pre- and postsynaptic APs. The changes in dynamics of signal transmission were accompanied by the reduction of presynaptic vGlut1 and ultrastructural changes in the perisynaptic space. These data show that brevican is an important mediator of fast synaptic transmission at the calyx of Held. ABSTRACT: The extracellular matrix is an integral part of the neural tissue. Its most conspicuous manifestation in the brain are the perineuronal nets (PNs) which surround somata and proximal dendrites of distinct neuron types. The chondroitin sulfate proteoglycan brevican is a major component of PNs. In contrast to other PN-comprising proteoglycans (e.g. aggrecan and neurocan), brevican is mainly expressed in the perisynaptic space closely associated with both the pre- and postsynaptic membrane. This specific localization prompted the hypothesis that brevican might play a role in synaptic transmission. In the present study we specifically investigated the role of brevican in synaptic transmission at a central synapse, the calyx of Held in the medial nucleus of the trapezoid body, by the use of in vivo electrophysiology, immunohistochemistry, biochemistry and electron microscopy. In vivo extracellular single-unit recordings were acquired in brevican-deficient mice and the dynamics and reliability of synaptic transmission were compared to wild-type littermates. In knockout mice, the speed of pre-to-postsynaptic action potential (AP) transmission was reduced and the duration of the respective pre- and postsynaptic APs increased. The reliability of signal transmission, however, was not affected by the lack of brevican. The changes in dynamics of signal transmission were accompanied by the reduction of (i) presynaptic vGlut1 and (ii) the size of subsynaptic cavities. The present results suggest an essential role of brevican for the functionality of high-speed synaptic transmission at the calyx of Held.

Indexed as

Acoustic StimulationAction PotentialsAnimalsBrevicanExcitatory Amino Acid Transporter 2Extracellular MatrixFemaleGlucose Transporter Type 1Glucose Transporter Type 2MaleMiceMice, Inbred C57BLMice, KnockoutSynapsesSynaptic TransmissionTrapezoid BodyBcan protein, mouseBrevicanExcitatory Amino Acid Transporter 2Glucose Transporter Type 1Glucose Transporter Type 2Slc1a2 protein, mouseSlc2a1 protein, mouseSlc2a2 protein, mouse

Identifiers

PMID26223835
PMCPMC4594243
OpenAlexW1546509016

What OpenQuestion holds

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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.