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Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice
Exposure to particulate matter (PM) is leading to various respiratory health outcomes. Compared to coarse and fine particles, less is known about the effects of chronic exposure to ultrafine particles, despite their higher number and reactivity. In the present study, we performed a time-course exper...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479904/ https://www.ncbi.nlm.nih.gov/pubmed/30987320 http://dx.doi.org/10.3390/ijerph16071210 |
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author | Saleh, Yara Antherieu, Sébastien Dusautoir, Romain Y. Alleman, Laurent Sotty, Jules De Sousa, Corentin Platel, Anne Perdrix, Esperanza Riffault, Véronique Fronval, Isabelle Nesslany, Fabrice Canivet, Ludivine Garçon, Guillaume Lo-Guidice, Jean-Marc |
author_facet | Saleh, Yara Antherieu, Sébastien Dusautoir, Romain Y. Alleman, Laurent Sotty, Jules De Sousa, Corentin Platel, Anne Perdrix, Esperanza Riffault, Véronique Fronval, Isabelle Nesslany, Fabrice Canivet, Ludivine Garçon, Guillaume Lo-Guidice, Jean-Marc |
author_sort | Saleh, Yara |
collection | PubMed |
description | Exposure to particulate matter (PM) is leading to various respiratory health outcomes. Compared to coarse and fine particles, less is known about the effects of chronic exposure to ultrafine particles, despite their higher number and reactivity. In the present study, we performed a time-course experiment in mice to better analyze the lung impact of atmospheric ultrafine particles, with regard to the effects induced by fine particles collected on the same site. Trace element and PAH analysis demonstrated the almost similar chemical composition of both particle fractions. Mice were exposed intranasally to FF or UFP according to acute (10, 50 or 100 µg of PM) and repeated (10 µg of PM 3 times a week during 1 or 3 months) exposure protocols. More particle-laden macrophages and even greater chronic inflammation were observed in the UFP-exposed mice lungs. Histological analyses revealed that about 50% of lung tissues were damaged in mice exposed to UFP for three months versus only 35% in FF-exposed mice. These injuries were characterized by alveolar wall thickening, macrophage infiltrations, and cystic lesions. Taken together, these results strongly motivate the update of current regulations regarding ambient PM concentrations to include UFP and limit their emission. |
format | Online Article Text |
id | pubmed-6479904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64799042019-04-29 Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice Saleh, Yara Antherieu, Sébastien Dusautoir, Romain Y. Alleman, Laurent Sotty, Jules De Sousa, Corentin Platel, Anne Perdrix, Esperanza Riffault, Véronique Fronval, Isabelle Nesslany, Fabrice Canivet, Ludivine Garçon, Guillaume Lo-Guidice, Jean-Marc Int J Environ Res Public Health Article Exposure to particulate matter (PM) is leading to various respiratory health outcomes. Compared to coarse and fine particles, less is known about the effects of chronic exposure to ultrafine particles, despite their higher number and reactivity. In the present study, we performed a time-course experiment in mice to better analyze the lung impact of atmospheric ultrafine particles, with regard to the effects induced by fine particles collected on the same site. Trace element and PAH analysis demonstrated the almost similar chemical composition of both particle fractions. Mice were exposed intranasally to FF or UFP according to acute (10, 50 or 100 µg of PM) and repeated (10 µg of PM 3 times a week during 1 or 3 months) exposure protocols. More particle-laden macrophages and even greater chronic inflammation were observed in the UFP-exposed mice lungs. Histological analyses revealed that about 50% of lung tissues were damaged in mice exposed to UFP for three months versus only 35% in FF-exposed mice. These injuries were characterized by alveolar wall thickening, macrophage infiltrations, and cystic lesions. Taken together, these results strongly motivate the update of current regulations regarding ambient PM concentrations to include UFP and limit their emission. MDPI 2019-04-04 2019-04 /pmc/articles/PMC6479904/ /pubmed/30987320 http://dx.doi.org/10.3390/ijerph16071210 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Saleh, Yara Antherieu, Sébastien Dusautoir, Romain Y. Alleman, Laurent Sotty, Jules De Sousa, Corentin Platel, Anne Perdrix, Esperanza Riffault, Véronique Fronval, Isabelle Nesslany, Fabrice Canivet, Ludivine Garçon, Guillaume Lo-Guidice, Jean-Marc Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice |
title | Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice |
title_full | Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice |
title_fullStr | Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice |
title_full_unstemmed | Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice |
title_short | Exposure to Atmospheric Ultrafine Particles Induces Severe Lung Inflammatory Response and Tissue Remodeling in Mice |
title_sort | exposure to atmospheric ultrafine particles induces severe lung inflammatory response and tissue remodeling in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479904/ https://www.ncbi.nlm.nih.gov/pubmed/30987320 http://dx.doi.org/10.3390/ijerph16071210 |
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