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The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice

BACKGROUND: Particulate matter (PM) has been associated with increased pulmonary and cardiovascular mortality and morbidity. Additionally, PM is known to exacerbate asthma. However, whether ambient PM exposure contributes to the onset of asthma, especially in non-atopic children and adults, is less...

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Autores principales: Huang, Kuo-Liang, Liu, Szu-Yuan, Chou, Charles C. K., Lee, Yi-Hsin, Cheng, Tsun-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330505/
https://www.ncbi.nlm.nih.gov/pubmed/28245275
http://dx.doi.org/10.1371/journal.pone.0173158
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author Huang, Kuo-Liang
Liu, Szu-Yuan
Chou, Charles C. K.
Lee, Yi-Hsin
Cheng, Tsun-Jen
author_facet Huang, Kuo-Liang
Liu, Szu-Yuan
Chou, Charles C. K.
Lee, Yi-Hsin
Cheng, Tsun-Jen
author_sort Huang, Kuo-Liang
collection PubMed
description BACKGROUND: Particulate matter (PM) has been associated with increased pulmonary and cardiovascular mortality and morbidity. Additionally, PM is known to exacerbate asthma. However, whether ambient PM exposure contributes to the onset of asthma, especially in non-atopic children and adults, is less conclusive. The current study aimed to evaluate the effects of size-fractioned PM on lung immune responses in healthy BALB/c mice. METHODS AND PRINCIPAL FINDINGS: We collected PM(10), PM(2.5), PM(1) and PM(0.1) samples from October 2012 to August 2013 in the Taipei Basin. These PM samples were representative of urban traffic pollution. The samples were extracted and sonicated in phosphate-buffered saline (PBS). Female BALB/c mice were exposed to the samples via intratracheal instillation at three different doses: 1.75 mg/kg (35 μg/per mouse), 5 mg/kg (100 μg/per mouse), and 12.5 mg/kg (250 μg/per mouse). The mice were exposed on days 0 and 7, and PBS alone was used as a control. Following the exposures, the expression profiles of inflammatory cells and cytokines in bronchoalveolar lavage fluid (BALF) were assessed. Exposure to PM(10) resulted in inflammatory responses, including the recruitment of neutrophils and the induction of T helper 1 (Th1) cell-related cytokine release, such as TNF-α and IFN-γ. Furthermore, an allergic immune response, including the recruitment of eosinophils and the up-regulation of T helper 2 (Th2) cell-related cytokine release, such as IL-5 and IL-13, was also observed in the BALF of mice exposed to PM(10). CONCLUSIONS: Our study showed that exposure to PM alone caused mixed Th1/Th2 inflammatory responses in healthy mice. These findings support the hypothesis that PM may contribute to the onset of asthma.
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spelling pubmed-53305052017-03-09 The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice Huang, Kuo-Liang Liu, Szu-Yuan Chou, Charles C. K. Lee, Yi-Hsin Cheng, Tsun-Jen PLoS One Research Article BACKGROUND: Particulate matter (PM) has been associated with increased pulmonary and cardiovascular mortality and morbidity. Additionally, PM is known to exacerbate asthma. However, whether ambient PM exposure contributes to the onset of asthma, especially in non-atopic children and adults, is less conclusive. The current study aimed to evaluate the effects of size-fractioned PM on lung immune responses in healthy BALB/c mice. METHODS AND PRINCIPAL FINDINGS: We collected PM(10), PM(2.5), PM(1) and PM(0.1) samples from October 2012 to August 2013 in the Taipei Basin. These PM samples were representative of urban traffic pollution. The samples were extracted and sonicated in phosphate-buffered saline (PBS). Female BALB/c mice were exposed to the samples via intratracheal instillation at three different doses: 1.75 mg/kg (35 μg/per mouse), 5 mg/kg (100 μg/per mouse), and 12.5 mg/kg (250 μg/per mouse). The mice were exposed on days 0 and 7, and PBS alone was used as a control. Following the exposures, the expression profiles of inflammatory cells and cytokines in bronchoalveolar lavage fluid (BALF) were assessed. Exposure to PM(10) resulted in inflammatory responses, including the recruitment of neutrophils and the induction of T helper 1 (Th1) cell-related cytokine release, such as TNF-α and IFN-γ. Furthermore, an allergic immune response, including the recruitment of eosinophils and the up-regulation of T helper 2 (Th2) cell-related cytokine release, such as IL-5 and IL-13, was also observed in the BALF of mice exposed to PM(10). CONCLUSIONS: Our study showed that exposure to PM alone caused mixed Th1/Th2 inflammatory responses in healthy mice. These findings support the hypothesis that PM may contribute to the onset of asthma. Public Library of Science 2017-02-28 /pmc/articles/PMC5330505/ /pubmed/28245275 http://dx.doi.org/10.1371/journal.pone.0173158 Text en © 2017 Huang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Huang, Kuo-Liang
Liu, Szu-Yuan
Chou, Charles C. K.
Lee, Yi-Hsin
Cheng, Tsun-Jen
The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice
title The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice
title_full The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice
title_fullStr The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice
title_full_unstemmed The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice
title_short The effect of size-segregated ambient particulate matter on Th1/Th2-like immune responses in mice
title_sort effect of size-segregated ambient particulate matter on th1/th2-like immune responses in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330505/
https://www.ncbi.nlm.nih.gov/pubmed/28245275
http://dx.doi.org/10.1371/journal.pone.0173158
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