Evidence map›Paper›PMID 36329102›Full record

ArticleScientific reports2022

P2X4 receptor stimulation enhances MrgprB2-mediated mast cell activation and pseudoallergic reactions in mice.

Kazuki Yoshida, Shota Tanihara, Yuki Miyashita, Kosuke Obayashi, Masa-Aki Ito, Kimiko Yamamoto, Toshiyashu Imai, Isao Matsuoka

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. IgE and non-IgE-mediated pathways in anaphylaxis.Seminars in immunopathology · 2025
    Review
  2. 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

8 authors at 3 institutions in 1 country.

Kazuki YoshidaLaboratory of Pharmacology, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, 370-0033, Japan. yoshida-k@takasaki-u.ac.jp.
Shota TaniharaLaboratory of Pharmacology, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, 370-0033, Japan.
Yuki MiyashitaLaboratory of Pharmacology, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, 370-0033, Japan.
Kosuke ObayashiLaboratory of Pharmacology, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, 370-0033, Japan.
Masa-Aki ItoLaboratory of Pharmacology, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, 370-0033, Japan.
Kimiko YamamotoDepartment of Biomedical Engineering, Graduate School of Medicine, The University of Tokyo, Tokyo, 113-0033, Japan.
Toshiyashu ImaiDiscovery Research Laboratories, Nippon Chemiphar Co., Ltd., Misato, Saitama, 341-0005, Japan.
Isao MatsuokaLaboratory of Pharmacology, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, 370-0033, Japan.
Takasaki University of Health and Welfare · JPNippon Chemiphar (Japan) · JPThe University of Tokyo · JP

Funding

Japan Society for the Promotion of Science 18K14925Japan Society for the Promotion of Science 19K07328Japan Society for the Promotion of Science 20K16010
6 · The paper itself

Abstract

Pseudoallergies caused by drugs make disease treatment difficult. Mas-relate G protein-coupled receptor X2 (MRGPRX2), which is specifically expressed in mast cells (MCs), has been implicated in pseudoallergies. High concentrations of therapeutic agents are typically required to stimulate MRGPRX2. Although regulatory mechanisms may enhance this response, the factors involved in this regulation are not well-understood. In this study, the effects of extracellular ATP on MC activation induced by MrgprB2, the mouse ortholog of human MRGPRX2, were examined in mouse peritoneal MCs (PMCs). ATP alone induced minimal PMC degranulation but markedly enhanced degranulation induced by the MrgprB2 agonist compound 48/80 (CP48/80), substance P, PAMP-12, and vancomycin. ATP promoted CP48/80-induced increase in intracellular Ca

Indexed as

AnaphylaxisCell DegranulationAdenosine TriphosphateAnimalsHumansMast CellsMiceMice, Inbred C57BLNerve Tissue ProteinsPhosphatidylinositol 3-KinasesReceptors, G-Protein-CoupledReceptors, NeuropeptideReceptors, Purinergic P2X4Adenosine TriphosphateMrgprb2 protein, mouseMRGPRX2 protein, humanNerve Tissue ProteinsPhosphatidylinositol 3-KinasesReceptors, G-Protein-CoupledReceptors, NeuropeptideReceptors, Purinergic P2X4

Identifiers

PMID36329102
PMCPMC9633816
OpenAlexW4308485494

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.