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Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa

Arsenic is the number one contaminant of concern with regard to human health according to the World Health Organization. Epidemiological studies on Asian and South American populations have linked arsenic exposure with an increased incidence of lung disease, including pneumonia, and chronic obstruct...

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Autores principales: Notch, Emily G., Goodale, Britton C., Barnaby, Roxanna, Coutermarsh, Bonita, Berwin, Brent, Taylor, Vivien F., Jackson, Brian P., Stanton, Bruce A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640536/
https://www.ncbi.nlm.nih.gov/pubmed/26554712
http://dx.doi.org/10.1371/journal.pone.0142392
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author Notch, Emily G.
Goodale, Britton C.
Barnaby, Roxanna
Coutermarsh, Bonita
Berwin, Brent
Taylor, Vivien F.
Jackson, Brian P.
Stanton, Bruce A.
author_facet Notch, Emily G.
Goodale, Britton C.
Barnaby, Roxanna
Coutermarsh, Bonita
Berwin, Brent
Taylor, Vivien F.
Jackson, Brian P.
Stanton, Bruce A.
author_sort Notch, Emily G.
collection PubMed
description Arsenic is the number one contaminant of concern with regard to human health according to the World Health Organization. Epidemiological studies on Asian and South American populations have linked arsenic exposure with an increased incidence of lung disease, including pneumonia, and chronic obstructive pulmonary disease, both of which are associated with bacterial infection. However, little is known about the effects of low dose arsenic exposure, or the contributions of organic arsenic to the innate immune response to bacterial infection. This study examined the effects on Pseudomonas aeruginosa (P. aeruginosa) induced cytokine secretion by human bronchial epithelial cells (HBEC) by inorganic sodium arsenite (iAs(III)) and two major metabolites, monomethylarsonous acid (MMA(III)) and dimethylarsenic acid (DMA(V)), at concentrations relevant to the U.S. population. Neither iAs(III) nor DMA(V) altered P. aeruginosa induced cytokine secretion. By contrast, MMA(III) increased P. aeruginosa induced secretion of IL-8, IL-6 and CXCL2. A combination of iAs(III), MMA(III) and DMA(V) (10 pbb total) reduced IL-8 and CXCL1 secretion. These data demonstrate for the first time that exposure to MMA(III) alone, and a combination of iAs(III), MMA(III) and DMA(V) at levels relevant to the U.S. may have negative effects on the innate immune response of human bronchial epithelial cells to P. aeruginosa.
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spelling pubmed-46405362015-11-13 Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa Notch, Emily G. Goodale, Britton C. Barnaby, Roxanna Coutermarsh, Bonita Berwin, Brent Taylor, Vivien F. Jackson, Brian P. Stanton, Bruce A. PLoS One Research Article Arsenic is the number one contaminant of concern with regard to human health according to the World Health Organization. Epidemiological studies on Asian and South American populations have linked arsenic exposure with an increased incidence of lung disease, including pneumonia, and chronic obstructive pulmonary disease, both of which are associated with bacterial infection. However, little is known about the effects of low dose arsenic exposure, or the contributions of organic arsenic to the innate immune response to bacterial infection. This study examined the effects on Pseudomonas aeruginosa (P. aeruginosa) induced cytokine secretion by human bronchial epithelial cells (HBEC) by inorganic sodium arsenite (iAs(III)) and two major metabolites, monomethylarsonous acid (MMA(III)) and dimethylarsenic acid (DMA(V)), at concentrations relevant to the U.S. population. Neither iAs(III) nor DMA(V) altered P. aeruginosa induced cytokine secretion. By contrast, MMA(III) increased P. aeruginosa induced secretion of IL-8, IL-6 and CXCL2. A combination of iAs(III), MMA(III) and DMA(V) (10 pbb total) reduced IL-8 and CXCL1 secretion. These data demonstrate for the first time that exposure to MMA(III) alone, and a combination of iAs(III), MMA(III) and DMA(V) at levels relevant to the U.S. may have negative effects on the innate immune response of human bronchial epithelial cells to P. aeruginosa. Public Library of Science 2015-11-10 /pmc/articles/PMC4640536/ /pubmed/26554712 http://dx.doi.org/10.1371/journal.pone.0142392 Text en © 2015 Notch 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Notch, Emily G.
Goodale, Britton C.
Barnaby, Roxanna
Coutermarsh, Bonita
Berwin, Brent
Taylor, Vivien F.
Jackson, Brian P.
Stanton, Bruce A.
Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa
title Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa
title_full Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa
title_fullStr Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa
title_full_unstemmed Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa
title_short Monomethylarsonous Acid (MMA(III)) Has an Adverse Effect on the Innate Immune Response of Human Bronchial Epithelial Cells to Pseudomonas aeruginosa
title_sort monomethylarsonous acid (mma(iii)) has an adverse effect on the innate immune response of human bronchial epithelial cells to pseudomonas aeruginosa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640536/
https://www.ncbi.nlm.nih.gov/pubmed/26554712
http://dx.doi.org/10.1371/journal.pone.0142392
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