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Cellular reactions to long-term volatile organic compound (VOC) exposures
Investigations of cellular processes initiated by volatile organic compounds (VOCs) are limited when modelling realistic long-term exposure scenarios at low concentrations. Exposure to indoor VOCs is associated with a range of adverse effects, but data on molecular changes at regulatory threshold li...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131358/ https://www.ncbi.nlm.nih.gov/pubmed/27905399 http://dx.doi.org/10.1038/srep37842 |
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author | Gostner, Johanna M. Zeisler, Johannes Alam, Mohammad Tauqeer Gruber, Peter Fuchs, Dietmar Becker, Kathrin Neubert, Kerstin Kleinhappl, Markus Martini, Stefan Überall, Florian |
author_facet | Gostner, Johanna M. Zeisler, Johannes Alam, Mohammad Tauqeer Gruber, Peter Fuchs, Dietmar Becker, Kathrin Neubert, Kerstin Kleinhappl, Markus Martini, Stefan Überall, Florian |
author_sort | Gostner, Johanna M. |
collection | PubMed |
description | Investigations of cellular processes initiated by volatile organic compounds (VOCs) are limited when modelling realistic long-term exposure scenarios at low concentrations. Exposure to indoor VOCs is associated with a range of adverse effects, but data on molecular changes at regulatory threshold limits are lacking. Activity analysis of VOC in vitro can be a valuable complement to inhalation toxicological evaluations. We developed an exposure platform that generates a stable VOC atmosphere and allows the exposure of cells for longer periods. Using formaldehyde as a model analyte, air-liquid interface cultured A549 lung epithelial cells were exposed to critical concentrations of 0.1 and 0.5 ppm for 3 days. Owing to the lack of known exposure biomarkers, we applied a genome-wide transcriptional analysis to investigate cellular responses at these sublethal concentrations. We demonstrate a minor overlap of differentially expressed transcripts for both treatment concentrations, which can be further analyzed for their use as exposure biomarkers. Moreover, distinct expression patterns emerge for 0.1 and 0.5 ppm formaldehyde exposure, which is reflected in significant enrichment of distinct biological processes. More specifically, metabolism of specific compound classes, lipid biosynthesis and lung-associated functions are affected by lower exposure levels and processes affecting proliferation and apoptosis dominate the higher exposure levels. |
format | Online Article Text |
id | pubmed-5131358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51313582016-12-15 Cellular reactions to long-term volatile organic compound (VOC) exposures Gostner, Johanna M. Zeisler, Johannes Alam, Mohammad Tauqeer Gruber, Peter Fuchs, Dietmar Becker, Kathrin Neubert, Kerstin Kleinhappl, Markus Martini, Stefan Überall, Florian Sci Rep Article Investigations of cellular processes initiated by volatile organic compounds (VOCs) are limited when modelling realistic long-term exposure scenarios at low concentrations. Exposure to indoor VOCs is associated with a range of adverse effects, but data on molecular changes at regulatory threshold limits are lacking. Activity analysis of VOC in vitro can be a valuable complement to inhalation toxicological evaluations. We developed an exposure platform that generates a stable VOC atmosphere and allows the exposure of cells for longer periods. Using formaldehyde as a model analyte, air-liquid interface cultured A549 lung epithelial cells were exposed to critical concentrations of 0.1 and 0.5 ppm for 3 days. Owing to the lack of known exposure biomarkers, we applied a genome-wide transcriptional analysis to investigate cellular responses at these sublethal concentrations. We demonstrate a minor overlap of differentially expressed transcripts for both treatment concentrations, which can be further analyzed for their use as exposure biomarkers. Moreover, distinct expression patterns emerge for 0.1 and 0.5 ppm formaldehyde exposure, which is reflected in significant enrichment of distinct biological processes. More specifically, metabolism of specific compound classes, lipid biosynthesis and lung-associated functions are affected by lower exposure levels and processes affecting proliferation and apoptosis dominate the higher exposure levels. Nature Publishing Group 2016-12-01 /pmc/articles/PMC5131358/ /pubmed/27905399 http://dx.doi.org/10.1038/srep37842 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gostner, Johanna M. Zeisler, Johannes Alam, Mohammad Tauqeer Gruber, Peter Fuchs, Dietmar Becker, Kathrin Neubert, Kerstin Kleinhappl, Markus Martini, Stefan Überall, Florian Cellular reactions to long-term volatile organic compound (VOC) exposures |
title | Cellular reactions to long-term volatile organic compound (VOC) exposures |
title_full | Cellular reactions to long-term volatile organic compound (VOC) exposures |
title_fullStr | Cellular reactions to long-term volatile organic compound (VOC) exposures |
title_full_unstemmed | Cellular reactions to long-term volatile organic compound (VOC) exposures |
title_short | Cellular reactions to long-term volatile organic compound (VOC) exposures |
title_sort | cellular reactions to long-term volatile organic compound (voc) exposures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131358/ https://www.ncbi.nlm.nih.gov/pubmed/27905399 http://dx.doi.org/10.1038/srep37842 |
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