Evidence map›Paper›PMID 35794670›Full record

ArticleParticle and fibre toxicology2022

The importance of mineralogical composition for the cytotoxic and pro-inflammatory effects of mineral dust.

Vegard Sæter Grytting, Magne Refsnes, Marit Låg, Eyolf Erichsen, Torkil Sørlie Røhr, Brynhild Snilsberg, Richard Aubrey White, Johan Øvrevik

Open access · goldAbstract read
In one paragraph

Article in Particle and fibre toxicology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Vegard Sæter GryttingDepartment of Air Quality and Noise, Division of Climate and Environmental Health, Norwegian Institute of Public Health, Skøyen, PO Box 222, 0213, Oslo, Norway. vegard.saeter.grytting@fhi.no.ORCID 0000-0003-0801-4223
Magne RefsnesDepartment of Air Quality and Noise, Division of Climate and Environmental Health, Norwegian Institute of Public Health, Skøyen, PO Box 222, 0213, Oslo, Norway.
Marit LågDepartment of Air Quality and Noise, Division of Climate and Environmental Health, Norwegian Institute of Public Health, Skøyen, PO Box 222, 0213, Oslo, Norway. marit.lag@fhi.no.
Eyolf ErichsenGeological Survey of Norway, Trondheim, Norway.
Torkil Sørlie RøhrGeological Survey of Norway, Trondheim, Norway.
Brynhild SnilsbergNorwegian Public Roads Administration, Trondheim, Norway.
Richard Aubrey WhiteDepartment of Method Development and Analytics, Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.
Johan ØvrevikDivision of Climate and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.
Norwegian Institute of Public Health · NOGeological Survey of Norway · NONorwegian Public Roads Administration · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRespirable mineral particles represent a potential health hazard in occupational settings and ambient air. Previous studies show that mineral particles may induce cytotoxicity and inflammatory reactions in vitro and in vivo and that the potency varies between samples of different composition. However, the reason for these differences is largely unknown and the impact of mineralogical composition on the biological effects of mineral dust remains to be determined.

methodsWe have assessed the cytotoxic and pro-inflammatory effects of ten mineral particle samples of different composition in human bronchial epithelial cells (HBEC3-KT) and THP-1-derived macrophages, as well as their membranolytic properties in erythrocytes. Moreover, the results were compiled with the results of recently published experiments on the effects of stone particle exposure and analysed using linear regression models to elucidate which mineral components contribute most to the toxicity of mineral dust.

resultsWhile all mineral particle samples were more cytotoxic to HBEC3-KT cells than THP-1 macrophages, biotite and quartz were among the most cytotoxic in both cell models. In HBEC3-KT cells, biotite and quartz also appeared to be the most potent inducers of pro-inflammatory cytokines, while the quartz, Ca-feldspar, Na-feldspar and biotite samples were the most potent in THP-1 macrophages. All particle samples except quartz induced low levels of membranolysis. The regression analyses revealed associations between particle bioactivity and the content of quartz, muscovite, plagioclase, biotite, anorthite, albite, microcline, calcite, chlorite, orthopyroxene, actinolite and epidote, depending on the cell model and endpoint. However, muscovite was the only mineral consistently associated with increased cytotoxicity and cytokine release in both cell models.

conclusionsThe present study provides further evidence that mineral particles may induce cytotoxicity and inflammation in cells of the human airways and that particle samples of different mineralogical composition differ in potency. The results show that quartz, while being among the most potent samples, does not fully predict the toxicity of mineral dust, highlighting the importance of other particle constituents. Moreover, the results indicate that the phyllosilicates muscovite and biotite may be more potent than other minerals assessed in the study, suggesting that this group of sheet-like minerals may warrant further attention.

Indexed as

DustQuartzCytokinesEpithelial CellsHumansInflammationMineralsCytokinesDustMineralsQuartzEpithelial cellsInflammationMacrophagesMineral particlesParticulate matterQuartzSilicaStone particles

Identifiers

PMID35794670
PMCPMC9261052
OpenAlexW4283835281

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.