Evidence map›Paper›PMID 17934511›Full record

ArticleBritish journal of pharmacology2007

P2X1 and P2X4 receptor currents in mouse macrophages.

J A Sim, C-K Park, S B Oh, R J Evans, R A North

Open access · greenAbstract read
In one paragraph

Article in British journal of pharmacology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 54 citations in OpenAlex.

  1. Holothurian triterpene glycoside cucumarioside ACancer cell international · 2023
    Article
  2. Article
  3. Article
  4. Dissection of P2X4 and P2X7 Receptor Current Components in BV-2 Microglia.International journal of molecular sciences · 2020
    Article
  5. Signaling Through Purinergic Receptor P2YInternational journal of molecular sciences · 2020
    Article
  6. Article
  7. P2X4 receptors, immunity, and sepsis.Current opinion in pharmacology · 2019
    Review
  8. Article
  9. Role of P2XScientific reports · 2018
    Article
  10. P2X4 Receptor-Dependent CaInternational journal of molecular sciences · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Heteromeric assembly of P2X subunits.Frontiers in cellular neuroscience · 2013
    Review
  19. Review
  20. 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

5 authors at 3 institutions in 2 countries.

J A SimFaculty of Life Sciences, University of Manchester, Manchester, Lancashire, UK. joan.sim@manchester.ac.uk
C-K Park
S B Oh
R J Evans
R A North
Seoul National University · KRUniversity of Manchester · GBUniversity of Leicester · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

background and purposeActivation of P2X receptors on macrophages is an important stimulus for cytokine release. This study seeks evidence for functional expression of P2X receptors in macrophages that had been only minimally activated. EXPERIMENTAL APPROACH: Whole-cell recordings were made from macrophages isolated 2-6 h before by lavage from mouse peritoneum, without further experimental activation. ATP (1-1000 muM) elicited inward currents in all cells (holding potential -60 mV). The properties of this current were compared among cells from wild type, P2X1 (-/-) and P2X4 (-/-) mice. KEY

resultsImmunoreactivity for P2X1 and P2X4 receptors was observed in wild type macrophages but was absent from the respective knock-out mice. In cells from wild type mice, ATP and alpha beta methyleneATP (alpha beta meATP) evoked inward currents rising in 10-30 ms and declining in 100-300 ms: these were blocked by pyridoxal-phosphate-6-azophenyl-2',4'-disulphonic acid (PPADS, 10 microM). ATP also elicited a second, smaller ( approximately 10% peak amplitude), more slowly decaying (1-3 s) at concentrations > or =10 microM: this was resistant to PPADS and prolonged by ivermectin. Macrophages from P2X1 (-/-) mice responded to ATP (>100 microM) but not alpha beta meATP: these small currents were prolonged by ivermectin. Macrophages from P2X4 (-/-) mice responded to ATP and alpha beta meATP as cells from wild type mice, except that ATP did not evoke the small, slowly decaying component: these currents were blocked by PPADS.

conclusionMouse peritoneal macrophages that are minimally activated demonstrate membrane currents in response to ATP and alpha beta meATP that have the predominate features of P2X1 receptors.

Indexed as

Adenosine TriphosphateAnimalsDose-Response Relationship, DrugElectrophysiologyIvermectinMacrophages, PeritonealMiceMice, Inbred C57BLMice, KnockoutPyridoxal PhosphateReceptors, Purinergic P2Receptors, Purinergic P2XReceptors, Purinergic P2X4Adenosine Triphosphatealpha,beta-methyleneadenosine 5'-triphosphateIvermectinP2rx4 protein, mousePyridoxal Phosphatepyridoxal phosphate-6-azophenyl-2',4'-disulfonic acidReceptors, Purinergic P2Receptors, Purinergic P2XReceptors, Purinergic P2X4

Identifiers

PMID17934511
PMCPMC2034508
OpenAlexW2107415303

What OpenQuestion holds

Textmetadata
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.