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Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells
Autoimmune diseases are complex disorders of unknown etiology thought to result from interactions between genetic and environmental factors. We aimed to verify whether environmental pollution from diesel engine exhaust nanoparticulate (DEP) of actually operating vehicles could play a role in the dev...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058589/ https://www.ncbi.nlm.nih.gov/pubmed/24982919 http://dx.doi.org/10.1155/2014/138751 |
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author | Mastrofrancesco, A. Alfè, M. Rosato, E. Gargiulo, V. Beatrice, C. Di Blasio, G. Zhang, B. Su, D. S. Picardo, M. Fiorito, S. |
author_facet | Mastrofrancesco, A. Alfè, M. Rosato, E. Gargiulo, V. Beatrice, C. Di Blasio, G. Zhang, B. Su, D. S. Picardo, M. Fiorito, S. |
author_sort | Mastrofrancesco, A. |
collection | PubMed |
description | Autoimmune diseases are complex disorders of unknown etiology thought to result from interactions between genetic and environmental factors. We aimed to verify whether environmental pollution from diesel engine exhaust nanoparticulate (DEP) of actually operating vehicles could play a role in the development of a rare immune-mediated disease, systemic sclerosis (SSc), in which the pathogenetic role of environment has been highlighted. The effects of carbon-based nanoparticulate collected at the exhaust of newer (Euro 5) and older (Euro 4) diesel engines on SSc skin keratinocytes and fibroblasts were evaluated in vitro by assessing the mRNA expression of inflammatory cytokines (IL-1α, IL-6, IL-8, and TNF-α) and fibroblast chemical mediators (metalloproteases 2, 3, 7, 9, and 12; collagen types I and III; VEGF). DEP was shown to stimulate cytokine gene expression at a higher extent in SSc keratinocytes versus normal cells. Moreover, the mRNA gene expression of all MMPs, collagen types, and VEGF genes was significantly higher in untreated SSc fibroblasts versus controls. Euro 5 particle exposure increased the mRNA expression of MMP-2, -7, and -9 in SSc fibroblasts in a dose dependent manner and only at the highest concentration in normal cells. We suggest that environmental DEP could trigger the development of SSc acting on genetically hyperreactive cell systems. |
format | Online Article Text |
id | pubmed-4058589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40585892014-06-30 Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells Mastrofrancesco, A. Alfè, M. Rosato, E. Gargiulo, V. Beatrice, C. Di Blasio, G. Zhang, B. Su, D. S. Picardo, M. Fiorito, S. J Immunol Res Research Article Autoimmune diseases are complex disorders of unknown etiology thought to result from interactions between genetic and environmental factors. We aimed to verify whether environmental pollution from diesel engine exhaust nanoparticulate (DEP) of actually operating vehicles could play a role in the development of a rare immune-mediated disease, systemic sclerosis (SSc), in which the pathogenetic role of environment has been highlighted. The effects of carbon-based nanoparticulate collected at the exhaust of newer (Euro 5) and older (Euro 4) diesel engines on SSc skin keratinocytes and fibroblasts were evaluated in vitro by assessing the mRNA expression of inflammatory cytokines (IL-1α, IL-6, IL-8, and TNF-α) and fibroblast chemical mediators (metalloproteases 2, 3, 7, 9, and 12; collagen types I and III; VEGF). DEP was shown to stimulate cytokine gene expression at a higher extent in SSc keratinocytes versus normal cells. Moreover, the mRNA gene expression of all MMPs, collagen types, and VEGF genes was significantly higher in untreated SSc fibroblasts versus controls. Euro 5 particle exposure increased the mRNA expression of MMP-2, -7, and -9 in SSc fibroblasts in a dose dependent manner and only at the highest concentration in normal cells. We suggest that environmental DEP could trigger the development of SSc acting on genetically hyperreactive cell systems. Hindawi Publishing Corporation 2014 2014-06-01 /pmc/articles/PMC4058589/ /pubmed/24982919 http://dx.doi.org/10.1155/2014/138751 Text en Copyright © 2014 A. Mastrofrancesco et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mastrofrancesco, A. Alfè, M. Rosato, E. Gargiulo, V. Beatrice, C. Di Blasio, G. Zhang, B. Su, D. S. Picardo, M. Fiorito, S. Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells |
title | Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells |
title_full | Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells |
title_fullStr | Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells |
title_full_unstemmed | Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells |
title_short | Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells |
title_sort | proinflammatory effects of diesel exhaust nanoparticles on scleroderma skin cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058589/ https://www.ncbi.nlm.nih.gov/pubmed/24982919 http://dx.doi.org/10.1155/2014/138751 |
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