Evidence map›Paper›PMID 31552031›Full record

ArticleFrontiers in immunology2019

Human Peripheral Blood Eosinophils Express High Levels of the Purinergic Receptor P2X4.

Viiu Paalme, Airi Rump, Kati Mädo, Marina Teras, Birgit Truumees, Helen Aitai, Kristel Ratas, Mickael Bourge, Chi-Shiun Chiang, Aram Ghalali and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

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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 7 institutions in 4 countries.

Viiu PaalmeImmunology Unit, Department of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.
Airi RumpImmunology Unit, Department of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.
Kati MädoNorth Estonia Medical Centre Foundation, Tallinn, Estonia.
Marina TerasNorth Estonia Medical Centre Foundation, Tallinn, Estonia.
Birgit TruumeesNorth Estonia Medical Centre Foundation, Tallinn, Estonia.
Helen AitaiImmunology Unit, Department of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.
Kristel RatasImmunology Unit, Department of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.
Mickael BourgeInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, Gif-sur-Yvette, France.
Chi-Shiun ChiangDepartment of Biomedical Engineering and Environmental Sciences, and Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing-Hua University, Hsinchu, Taiwan.
Aram GhalaliInstitute of Environment Medicine, Karolinska Institutet, Stockholm, Sweden.
Thierry TordjmannINSERM U1174 Université Paris Sud, Orsay, France.
Jüri TerasNorth Estonia Medical Centre Foundation, Tallinn, Estonia.
Pierre BoudinotVirologie et Immunologie Moléculaires, INRA, Université Paris Saclay, Jouy en Josas, France.
Jean M KanellopoulosDepartment of Biochemistry Biophysics and Structural Biology, I2BC-CNRS, Université Paris-Sud, Orsay, France.
Sirje Rüütel BoudinotImmunology Unit, Department of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.
Tallinn University of Technology · EENorth Estonia Medical Centre · EEUniversité Paris-Sud · FRInserm · FRKarolinska Institutet · SENational Tsing Hua University · TWUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular nucleotides are important mediators of cell activation and trigger multiple responses via membrane receptors known as purinergic receptors (P2). P2X receptors are ligand-gated ion channels, activated by extracellular ATP. P2X4 is one of the most sensitive purinergic receptors, that is typically expressed by neurons, microglia, and some epithelial and endothelial cells. P2X4 mediates neuropathic pain via brain-derived neurotrophic factor and is also involved in inflammation in response to high ATP release. It is therefore involved in multiple inflammatory pathologies as well as neurodegenerative diseases. We have produced monoclonal antibodies (mAb) directed against this important human P2X4 receptor. Focusing on two mAbs, we showed that they also recognize mouse and rat P2X4. We demonstrated that these mAbs can be used in flow cytometry, immunoprecipitation, and immunohistochemistry, but not in Western blot assays, indicating that they target conformational epitopes. We also characterized the expression of P2X4 receptor on mouse and human peripheral blood lymphocytes (PBL). We showed that P2X4 is expressed at the surface of several leukocyte cell types, with the highest expression level on eosinophils, making them potentially sensitive to adenosine triphosphate (ATP). P2X4 is expressed by leucocytes, in human and mouse, with a significant gender difference, males having higher surface expression levels than females. Our findings reveal that PBL express significant levels of P2X4 receptor, and suggest an important role of this receptor in leukocyte activation by ATP, particularly in P2X4

Indexed as

Gene ExpressionAnimalsAstrocytomaBiomarkersCell LineEosinophilsFemaleGliomaHumansImmunophenotypingLeukocytesMaleMiceMicrogliaReceptors, Purinergic P2X4BiomarkersReceptors, Purinergic P2X4eosinophilsgender differencemonoclonal antibodyP2X4 purinergic receptorPBL marker

Identifiers

PMID31552031
PMCPMC6746186
OpenAlexW2969197037

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.