Evidence map›Paper›PMID 33187309›Full record

ArticleInternational journal of molecular sciences2020

Dissection of P2X4 and P2X7 Receptor Current Components in BV-2 Microglia.

Mira Trang, Günther Schmalzing, Christa E Müller, Fritz Markwardt

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  8. Animal Models for the Investigation of P2X7 Receptors.International journal of molecular sciences · 2023
    Review
  9. Review
  10. Modulation of P2XPhysiological reports · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. P2X7 receptor: a critical regulator and potential target for breast cancer.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  17. 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

4 authors at 3 institutions in 1 country.

Mira TrangJulius-Bernstein-Institute for Physiology, Martin-Luther-University, D-06097 Halle-Wittenberg, Germany.
Günther SchmalzingInstitute of Clinical Pharmacology, RWTH Aachen University, D-52074 Aachen, Germany.
Christa E MüllerPharmaceutical Institute, Pharmaceutical & Mediinal Chemistry, University of Bonn, D-53121 Bonn, Germany.ORCID 0000-0002-0013-6624
Fritz MarkwardtJulius-Bernstein-Institute for Physiology, Martin-Luther-University, D-06097 Halle-Wittenberg, Germany.ORCID 0000-0001-6761-2923
Martin Luther University Halle-Wittenberg · DERWTH Aachen University · DEUniversity of Bonn · DE

Funding

Deutsche Forschungsgemeinschaft MA 1581/15-2Deutsche Forschungsgemeinschaft Schm 536/9-2
6 · The paper itself

Abstract

Microglia cells represent the immune system of the central nervous system. They become activated by ATP released from damaged and inflamed tissue via purinergic receptors. Ionotropic purinergic P2X4 and P2X7 receptors have been shown to be involved in neurological inflammation and pain sensation. Whether the two receptors assemble exclusively as homotrimers or also as heterotrimers is still a matter of debate. We investigated the expression of P2X receptors in BV-2 microglia cells applying the whole-cell voltage-clamp technique. We dissected P2X4 and P2X7 receptor-mediated current components by using specific P2X4 and P2X7 receptor blockers and by their characteristic current kinetics. We found that P2X4 and P2X7 receptors are activated independently from each other, indicating that P2X4/P2X7 heteromers are not of functional significance in these cells. The pro-inflammatory mediators lipopolysaccharide and interferon γ, if applied in combination, upregulated P2X4, but not P2X7 receptor-dependent current components also arguing against phenotypically relevant heteromerization of P2X4 and P2X7 receptor subunits.

Indexed as

AnimalsCells, CulturedFemaleInterferon-gammaLipopolysaccharidesMiceMicrogliaPatch-Clamp TechniquesProtein SubunitsPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X4Receptors, Purinergic P2X7Up-RegulationXenopus laevisInterferon-gammaLipopolysaccharidesP2rx7 protein, mouseProtein SubunitsPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X4Receptors, Purinergic P2X7microgliaP2 purinergic receptorP2X4 receptorP2X7 receptorvoltage clamp

Identifiers

PMID33187309
PMCPMC7696836
OpenAlexW3104536997

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.