Evidence map›Paper›PMID 28158279›Full record

ArticlePloS one2017

Analysis of TRPV channel activation by stimulation of FCεRI and MRGPR receptors in mouse peritoneal mast cells.

A Solís-López, U Kriebs, A Marx, S Mannebach, W B Liedtke, M J Caterina, M Freichel, V V Tsvilovskyy

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. FcεR1-expressing nociceptors trigger allergic airway inflammation.The Journal of allergy and clinical immunology · 2021
    Article
  6. Review
  7. A Critical Role for NaJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  8. Article
  9. Involvement of Mast Cells in the Pathophysiology of Pain.Frontiers in cellular neuroscience · 2021
    Article
  10. Article
  11. Article
  12. Analysis of Mrgprb2 Receptor-Evoked CaFrontiers in immunology · 2020
    Article
  13. Review
  14. Article
  15. 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

8 authors at 4 institutions in 2 countries.

A Solís-LópezPharmakologisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Baden-Württemberg, Germany.
U KriebsPharmakologisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Baden-Württemberg, Germany.
A MarxPharmakologisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Baden-Württemberg, Germany.
S MannebachExperimentelle und Klinische Pharmakologie und Toxikologie, Universität des Saarlandes, Homburg, Saarland, Germany.
W B LiedtkeDepartment of Neurology, School of Medicine Duke University, Durham, North Carolina, United States of America.
M J CaterinaDepartments of Neurosurgery, Biological Chemistry, and Neuroscience, Neurosurgery Pain Research Institute, The Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.
M FreichelPharmakologisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Baden-Württemberg, Germany.
V V TsvilovskyyPharmakologisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Baden-Württemberg, Germany.
Heidelberg University · DEDuke University · USJohns Hopkins Medicine · USSaarland University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The activation of mast cells (MC) is part of the innate and adaptive immune responses and depends on Ca2+ entry across the plasma membrane, leading to the release of preformed inflammatory mediators by degranulation or by de novo synthesis. The calcium conducting channels of the TRPV family, known by their thermo and osmotic sensitivity, have been proposed to be involved in the MC activation in murine, rat, and human mast cell models. So far, immortalized mast cell lines and nonspecific TRPV blockers have been employed to characterize the role of TRPV channels in MC. The aim of this work was to elucidate the physiological role of TRPV channels by using primary peritoneal mast cells (PMCs), a model of connective tissue type mast cells. Our RT-PCR and NanoString analysis identified the expression of TRPV1, TRPV2, and TRPV4 channels in PMCs. For determination of the functional role of the expressed TRPV channels we performed measurements of intracellular free Ca2+ concentrations and beta-hexosaminidase release in PMCs obtained from wild type and mice deficient for corresponding TRPV1, TRPV2 and TRPV4 in response to various receptor-mediated and physical stimuli. Furthermore, substances known as activators of corresponding TRPV-channels were also tested using these assays. Our results demonstrate that TRPV1, TRPV2, and TRPV4 do not participate in activation pathways triggered by activation of the high-affinity receptors for IgE (FcεRI), Mrgprb2 receptor, or Endothelin-1 receptor nor by heat or osmotic stimulation in mouse PMCs.

Indexed as

AnimalsCalciumCalcium ChannelsCells, CulturedEndothelin-1Mast CellsMicePeritoneump-Methoxy-N-methylphenethylamineReceptors, G-Protein-CoupledReceptors, IgEReverse Transcriptase Polymerase Chain ReactionTRPV Cation ChannelsCalciumCalcium ChannelsEndothelin-1Mrgprb2 protein, mousep-Methoxy-N-methylphenethylamineReceptors, G-Protein-CoupledReceptors, IgETRPV1 protein, mouseTrpv2 protein, mouseTrpv4 protein, mouseTRPV Cation Channels

Identifiers

PMID28158279
PMCPMC5291405
OpenAlexW2583185711

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.