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The dependence of particle size on cell toxicity for modern mining dust

Progressive massive pulmonary fibrosis among coal miners has unexpectedly increased. It would likely due to the greater generation of smaller rock and coal particles produced by powerful equipment used in modern mines. There is limited understanding of the relationship between micro- or nanoparticle...

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Autores principales: Chen, Yi-Hsuan, Nguyen, Dorothy, Brindley, Stephen, Ma, Tiancong, Xia, Tian, Brune, Jürgen, Brown, Jared M., Tsai, Candace Su-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060429/
https://www.ncbi.nlm.nih.gov/pubmed/36991007
http://dx.doi.org/10.1038/s41598-023-31215-5
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author Chen, Yi-Hsuan
Nguyen, Dorothy
Brindley, Stephen
Ma, Tiancong
Xia, Tian
Brune, Jürgen
Brown, Jared M.
Tsai, Candace Su-Jung
author_facet Chen, Yi-Hsuan
Nguyen, Dorothy
Brindley, Stephen
Ma, Tiancong
Xia, Tian
Brune, Jürgen
Brown, Jared M.
Tsai, Candace Su-Jung
author_sort Chen, Yi-Hsuan
collection PubMed
description Progressive massive pulmonary fibrosis among coal miners has unexpectedly increased. It would likely due to the greater generation of smaller rock and coal particles produced by powerful equipment used in modern mines. There is limited understanding of the relationship between micro- or nanoparticles with pulmonary toxicity. This study aims to determine whether the size and chemical characteristics of typical coal-mining dust contribute to cellular toxicity. Size range, surface features, morphology, and elemental composition of coal and rock dust from modern mines were characterized. Human macrophages and bronchial tracheal epithelial cells were exposed to mining dust of three sub- micrometer and micrometer size ranges at varying concentrations, then assessed for cell viability and inflammatory cytokine expression. Coal had smaller hydrodynamic size (180–3000 nm) compared to rock (495–2160 nm) in their separated size fractions, more hydrophobicity, less surface charge, and consisted of more known toxic trace elements (Si, Pt, Fe, Al, Co). Larger particle size had a negative association with in-vitro toxicity in macrophages (p < 0.05). Fine particle fraction, approximately 200 nm for coal and 500 nm for rock particles, explicitly induced stronger inflammatory reactions than their coarser counterparts. Future work will study additional toxicity endpoints to further elucidate the molecular mechanism causing pulmonary toxicity and determine a dose–response curve.
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spelling pubmed-100604292023-03-31 The dependence of particle size on cell toxicity for modern mining dust Chen, Yi-Hsuan Nguyen, Dorothy Brindley, Stephen Ma, Tiancong Xia, Tian Brune, Jürgen Brown, Jared M. Tsai, Candace Su-Jung Sci Rep Article Progressive massive pulmonary fibrosis among coal miners has unexpectedly increased. It would likely due to the greater generation of smaller rock and coal particles produced by powerful equipment used in modern mines. There is limited understanding of the relationship between micro- or nanoparticles with pulmonary toxicity. This study aims to determine whether the size and chemical characteristics of typical coal-mining dust contribute to cellular toxicity. Size range, surface features, morphology, and elemental composition of coal and rock dust from modern mines were characterized. Human macrophages and bronchial tracheal epithelial cells were exposed to mining dust of three sub- micrometer and micrometer size ranges at varying concentrations, then assessed for cell viability and inflammatory cytokine expression. Coal had smaller hydrodynamic size (180–3000 nm) compared to rock (495–2160 nm) in their separated size fractions, more hydrophobicity, less surface charge, and consisted of more known toxic trace elements (Si, Pt, Fe, Al, Co). Larger particle size had a negative association with in-vitro toxicity in macrophages (p < 0.05). Fine particle fraction, approximately 200 nm for coal and 500 nm for rock particles, explicitly induced stronger inflammatory reactions than their coarser counterparts. Future work will study additional toxicity endpoints to further elucidate the molecular mechanism causing pulmonary toxicity and determine a dose–response curve. Nature Publishing Group UK 2023-03-29 /pmc/articles/PMC10060429/ /pubmed/36991007 http://dx.doi.org/10.1038/s41598-023-31215-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chen, Yi-Hsuan
Nguyen, Dorothy
Brindley, Stephen
Ma, Tiancong
Xia, Tian
Brune, Jürgen
Brown, Jared M.
Tsai, Candace Su-Jung
The dependence of particle size on cell toxicity for modern mining dust
title The dependence of particle size on cell toxicity for modern mining dust
title_full The dependence of particle size on cell toxicity for modern mining dust
title_fullStr The dependence of particle size on cell toxicity for modern mining dust
title_full_unstemmed The dependence of particle size on cell toxicity for modern mining dust
title_short The dependence of particle size on cell toxicity for modern mining dust
title_sort dependence of particle size on cell toxicity for modern mining dust
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060429/
https://www.ncbi.nlm.nih.gov/pubmed/36991007
http://dx.doi.org/10.1038/s41598-023-31215-5
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