Evidence map›Paper›PMID 18572241›Full record

ArticleCell calcium2008

Synergistic regulation of endogenous TRPM2 channels by adenine dinucleotides in primary human neutrophils.

Ingo Lange, Reinhold Penner, Andrea Fleig, Andreas Beck

Open access · greenAbstract read
In one paragraph

Article in Cell calcium, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
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  8. Dual amplification strategy turns TRPM2 channels into supersensitive central heat detectors.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Distribution and Assembly of TRP Ion Channels.Advances in experimental medicine and biology · 2021
    Article
  17. Review
  18. Roles of NADMolecules (Basel, Switzerland) · 2020
    Review
  19. Review
  20. Review

7 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Ingo LangeLaboratory of Cell and Molecular Signaling, Center for Biomedical Research at The Queen's Medical Center and John A. Burns School of Medicine at the University of Hawaii, Honolulu, HI 96813, United States.
Reinhold Penner
Andrea Fleig
Andreas Beck
Queen's Medical Center · USUniversity of Hawaii System · US

Funding

Molecular and functional properties of the TRPM2 catioin channelR01GM063954 · NIGMS · QUEEN'S MEDICAL CENTER · PI PENNER, REINHOLD · 2002 to 2010
$2.4M
Role of TRPV cation channels in mast cellsR01GM070634 · NIGMS · QUEEN'S MEDICAL CENTER · PI FLEIG, ANDREA · 2004 to 2008
$1.6M
NIGMS NIH HHS R01 GM063954NIGMS NIH HHS R01-GM063954NIGMS NIH HHS R01 GM070634NIGMS NIH HHS R01-GM070634
6 · The paper itself

Abstract

The Ca(2+)-permeable TRPM2 channel is a dual function protein that is activated by intracellular ADPR through its enzymatic pyrophosphatase domain with Ca(2+) acting as a co-factor. Other TRPM2 regulators include cADPR, NAADP and H(2)O(2), which synergize with ADPR to potentiate TRPM2 activation. Although TRPM2 has been thoroughly characterized in overexpression or cell-line systems, little is known about the features of TRPM2 in primary cells. We here characterize the regulation of TRPM2 activation in human neutrophils and report that ADPR activates TRPM2 with an effective half-maximal concentration (EC(50)) of 1microM. Potentiation by Ca(2+) is dose-dependent with an EC(50) of 300nM. Both cADPR and NAADP activate TRPM2, albeit with lower efficacy than in the presence of subthreshold levels of ADPR (100nM), which significantly shifts the EC(50) for cADPR from 44 to 3muM and for NAADP from 95 to 1microM. TRPM2 activation by ADPR can be suppressed by AMP with an IC(50) of 10microM and cADPR-induced activation can be blocked by 8-Bromo-cADPR. We further show that 100microM H(2)O(2) enables subthreshold concentrations of ADPR (100nM) to activate TRPM2. We conclude that agonistic and antagonistic characteristics of TRPM2 as seen in overexpression systems are largely compatible with the functional properties of TRPM2 currents measured in human neutrophils, but the potencies of agonists in primary cells are significantly higher.

Indexed as

Adenine NucleotidesAnimalsCalciumCells, CulturedCyclic ADP-RiboseHumansHydrogen PeroxideIntracellular SpaceIon Channel GatingMiceNADPNeutrophilsPatch-Clamp TechniquesTRPM Cation ChannelsAdenine NucleotidesCalciumCyclic ADP-RiboseHydrogen PeroxideNAADPNADPTRPM2 protein, humanTRPM Cation Channels

Identifiers

PMID18572241
PMCPMC2597220
OpenAlexW2168838919

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.