Evidence map›Paper›PMID 31077146›Full record

ArticleBMC immunology2019

Identification and characterisation of transient receptor potential melastatin 2 and CD38 channels on natural killer cells using the novel application of flow cytometry.

Cassandra Balinas, Helene Cabanas, Donald Staines, Sonya Marshall-Gradisnik

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
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  3. Article
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 1 institution in 1 country.

Cassandra BalinasSchool of Medical Science, Griffith University, Gold Coast, QLD, Australia. cassandra.balinas@griffithuni.edu.au.ORCID 0000-0001-8797-8906
Helene CabanasSchool of Medical Science, Griffith University, Gold Coast, QLD, Australia.
Donald StainesSchool of Medical Science, Griffith University, Gold Coast, QLD, Australia.
Sonya Marshall-GradisnikSchool of Medical Science, Griffith University, Gold Coast, QLD, Australia.
Griffith University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNatural Killer (NK) cells are effector lymphocytes of the innate immune system and are subclassed into CD56

resultsAt 2 h/1 h, TRPM2 (Fig. 2 A, B, p < 0.05) and TRPM2/CD38 (Fig. 3A, B, p < 0.05) surface expression significantly increased between 1:300 and 1:50 at 2 h/1 h. TRPM2/CD38 surface expression furthermore increased between 1:100 and 1:50 at 2 h/1 h (Fig. 3A, p < 0.05). Interestingly, TRPM2/CD38 surface expression significantly decreased from 1:50 to 1:5 on CD56

conclusionFor the first time, we describe an in vitro methodology to characterise TRPM2 and CD38 surface expression on NK cells in healthy participants. Finally, using an antibody that has not been previously applied in flow cytometry, we determined an antibody concentration and incubation time that is robust, rapid and sensitive for the application of flow cytometry.

Indexed as

ADP-ribosyl Cyclase 1Calcium SignalingCD56 AntigenCells, CulturedCell SeparationCytotoxicity, ImmunologicFlow CytometryGene Expression RegulationHealthy VolunteersHumansKiller Cells, NaturalTRPM Cation ChannelsADP-ribosyl Cyclase 1CD56 AntigenTRPM2 protein, humanTRPM Cation ChannelsAntibodyFlow cytometryNatural killer cellsTransient receptor potential Melastatin 2

Identifiers

PMID31077146
PMCPMC6509826
OpenAlexW2946884325

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.