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Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice

Pulmonary exposure to multi-walled carbon nanotubes (MWCNTs) has been linked to an increased risk of developing cardiovascular disease in addition to the well-documented physicochemical-dependent adverse lung effects. A proposed mechanism is through a strong and sustained pulmonary secretion of acut...

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Autores principales: Poulsen, Sarah S., Knudsen, Kristina B., Jackson, Petra, Weydahl, Ingrid E. K., Saber, Anne T., Wallin, Håkan, Vogel, Ulla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381870/
https://www.ncbi.nlm.nih.gov/pubmed/28380028
http://dx.doi.org/10.1371/journal.pone.0174167
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author Poulsen, Sarah S.
Knudsen, Kristina B.
Jackson, Petra
Weydahl, Ingrid E. K.
Saber, Anne T.
Wallin, Håkan
Vogel, Ulla
author_facet Poulsen, Sarah S.
Knudsen, Kristina B.
Jackson, Petra
Weydahl, Ingrid E. K.
Saber, Anne T.
Wallin, Håkan
Vogel, Ulla
author_sort Poulsen, Sarah S.
collection PubMed
description Pulmonary exposure to multi-walled carbon nanotubes (MWCNTs) has been linked to an increased risk of developing cardiovascular disease in addition to the well-documented physicochemical-dependent adverse lung effects. A proposed mechanism is through a strong and sustained pulmonary secretion of acute phase proteins to the blood. We identified physicochemical determinants of MWCNT-induced systemic acute phase response by analyzing effects of pulmonary exposure to 14 commercial, well-characterized MWCNTs in female C57BL/6J mice pulmonary exposed to 0, 6, 18 or 54 μg MWCNT/mouse. Plasma levels of acute phase response proteins serum amyloid A1/2 (SAA1/2) and SAA3 were determined on day 1, 28 or 92. Expression levels of hepatic Saa1 and pulmonary Saa3 mRNA levels were assessed to determine the origin of the acute phase response proteins. Pulmonary Saa3 mRNA expression levels were greater and lasted longer than hepatic Saa1 mRNA expression. Plasma SAA1/2 and SAA3 protein levels were related to time and physicochemical properties using adjusted, multiple regression analyses. SAA3 and SAA1/2 plasma protein levels were increased after exposure to almost all of the MWCNTs on day 1, whereas limited changes were observed on day 28 and 92. SAA1/2 and SAA3 protein levels did not correlate and only SAA3 protein levels correlated with neutrophil influx. The multiple regression analyses revealed a protective effect of MWCNT length on SAA1/2 protein level on day 1, such that a longer length resulted in lowered SAA1/2 plasma levels. Increased SAA3 protein levels were positively related to dose and content of Mn, Mg and Co on day 1, whereas oxidation and diameter of the MWCNTs were protective on day 28 and 92, respectively. The results of this study reveal very differently controlled pulmonary and hepatic acute phase responses after MWCNT exposure. As the responses were influenced by the physicochemical properties of the MWCNTs, this study provides the first step towards designing MWCNT that induce less SAA.
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spelling pubmed-53818702017-04-19 Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice Poulsen, Sarah S. Knudsen, Kristina B. Jackson, Petra Weydahl, Ingrid E. K. Saber, Anne T. Wallin, Håkan Vogel, Ulla PLoS One Research Article Pulmonary exposure to multi-walled carbon nanotubes (MWCNTs) has been linked to an increased risk of developing cardiovascular disease in addition to the well-documented physicochemical-dependent adverse lung effects. A proposed mechanism is through a strong and sustained pulmonary secretion of acute phase proteins to the blood. We identified physicochemical determinants of MWCNT-induced systemic acute phase response by analyzing effects of pulmonary exposure to 14 commercial, well-characterized MWCNTs in female C57BL/6J mice pulmonary exposed to 0, 6, 18 or 54 μg MWCNT/mouse. Plasma levels of acute phase response proteins serum amyloid A1/2 (SAA1/2) and SAA3 were determined on day 1, 28 or 92. Expression levels of hepatic Saa1 and pulmonary Saa3 mRNA levels were assessed to determine the origin of the acute phase response proteins. Pulmonary Saa3 mRNA expression levels were greater and lasted longer than hepatic Saa1 mRNA expression. Plasma SAA1/2 and SAA3 protein levels were related to time and physicochemical properties using adjusted, multiple regression analyses. SAA3 and SAA1/2 plasma protein levels were increased after exposure to almost all of the MWCNTs on day 1, whereas limited changes were observed on day 28 and 92. SAA1/2 and SAA3 protein levels did not correlate and only SAA3 protein levels correlated with neutrophil influx. The multiple regression analyses revealed a protective effect of MWCNT length on SAA1/2 protein level on day 1, such that a longer length resulted in lowered SAA1/2 plasma levels. Increased SAA3 protein levels were positively related to dose and content of Mn, Mg and Co on day 1, whereas oxidation and diameter of the MWCNTs were protective on day 28 and 92, respectively. The results of this study reveal very differently controlled pulmonary and hepatic acute phase responses after MWCNT exposure. As the responses were influenced by the physicochemical properties of the MWCNTs, this study provides the first step towards designing MWCNT that induce less SAA. Public Library of Science 2017-04-05 /pmc/articles/PMC5381870/ /pubmed/28380028 http://dx.doi.org/10.1371/journal.pone.0174167 Text en © 2017 Poulsen 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
Poulsen, Sarah S.
Knudsen, Kristina B.
Jackson, Petra
Weydahl, Ingrid E. K.
Saber, Anne T.
Wallin, Håkan
Vogel, Ulla
Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice
title Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice
title_full Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice
title_fullStr Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice
title_full_unstemmed Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice
title_short Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice
title_sort multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381870/
https://www.ncbi.nlm.nih.gov/pubmed/28380028
http://dx.doi.org/10.1371/journal.pone.0174167
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