Evidence map›Paper›PMID 23742824›Full record

ArticleBiochimica et biophysica acta2013

Kinetics of extracellular ATP in mastoparan 7-activated human erythrocytes.

María Florencia Leal Denis, J Jeremías Incicco, María Victoria Espelt, Sandra V Verstraeten, Omar P Pignataro, Eduardo R Lazarowski, Pablo J Schwarzbaum

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Evolution of Mechanical Stress (Archives of Razi Institute · 2021
    Article
  7. Pannexin 1 channels control the hemodynamic response to hypoxia by regulating OAmerican journal of physiology. Heart and circulatory physiology · 2021
    Article
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  10. Article
  11. Review
  12. Review
  13. Article
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

María Florencia Leal DenisDepartment of Biological Chemistry, University of Buenos Aires, Buenos Aires, Argentina.
J Jeremías Incicco
María Victoria Espelt
Sandra V Verstraeten
Omar P Pignataro
Eduardo R Lazarowski
Pablo J Schwarzbaum
Instituto de Química y Fisicoquímica Biológicas · ARUniversity of Buenos Aires · ARExperimental Medicine and Biology Institute · ARUniversity of North Carolina at Chapel Hill · US

Funding

Purinergic Control of CFTR-ENaC Interactions in Alveolar EpitheliaP01HL110873 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BOUCHER, RICHARD CHARLES · 2012 to 2016
$10.7M
NHLBI NIH HHS P01 HL110873NHLBI NIH HHS P01-HL-110873
6 · The paper itself

Abstract

backgroundThe peptide mastoparan 7 (MST7) stimulated ATP release in human erythrocytes. We explored intra- and extracellular processes governing the time-dependent accumulation of extracellular ATP (i.e., ATPe kinetics).

methodsHuman erythrocytes were treated with MST7 in the presence or absence of two blockers of pannexin 1. ATPe concentration was monitored by luciferin-luciferase based real-time luminometry.

resultsExposure of human erythrocytes to MST7 led to an acute increase in [ATPe], followed by a slower increase phase. ATPe kinetics reflected a strong activation of ATP efflux and a low rate of ATPe hydrolysis by ectoATPase activity. Enhancement of [ATPe] by MST7 required adhesion of erythrocytes to poly-D-lysin-coated coverslips, and correlated with a 31% increase of cAMP and 10% cell swelling. However, when MST7 was dissolved in a hyperosmotic medium to block cell swelling, ATPe accumulation was inhibited by 49%. Erythrocytes pre-exposure to 10μM of either carbenoxolone or probenecid, two blockers of pannexin 1, exhibited a partial reduction of ATP efflux. Erythrocytes from pannexin 1 knockout mice exhibited similar ATPe kinetics as those of wild type mice erythrocytes exposed to pannexin 1 blockers.

conclusionsMST7 induced release of ATP required either cell adhesion or strong activation of cAMP synthesis. Part of this release required cell swelling. Kinetic analysis and a data driven model suggested that ATP efflux is mediated by two ATP conduits displaying different kinetics, with one conduit being fully blocked by pannexin 1 blockers. GENERAL SIGNIFICANCE: Kinetic analysis of extracellular ATP accumulation from human erythrocytes and potential effects on microcirculation.

Indexed as

Adenosine TriphosphateAnimalsDogsErythrocytesHumansHydrolysisIntercellular Signaling Peptides and ProteinsKineticsMiceMice, KnockoutPeptidesSignal TransductionAdenosine TriphosphateIntercellular Signaling Peptides and ProteinsMas7 protein, syntheticPeptides3Va cAMP activating cocktail containing isoproterenol, forskolin and papaverineATPasesATPeATPicarbenoxoloneCBXcilostazolCTZErythrocyteextracellular ATPExtracellular ATPflux of ATPe hydrolysisflux of ATP releaseGEFsguanine exchange factorsintracellular ATPJ(R)J(V)mastoparanMSTpannexin 1Pannexin 1pannexin 1 heterozygous micepannexin 1 knockout mice, PTX, pertussis toxinpannexin 1 wild type micePBCpnxpnx(+/+)pnx(+/−)pnx(−/−)probenecidrbcsred blood cellsrelative cell volumeVr

Identifiers

PMID23742824
PMCPMC3999873
OpenAlexW1989813215

What OpenQuestion holds

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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.