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Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells

BACKGROUND: Exposures to an amphibole fiber in Libby, Montana cause increases in malignant mesothelioma (MM), a tumor of the pleural and peritoneal cavities with a poor prognosis. Affymetrix microarray/GeneSifter analysis was used to determine alterations in gene expression of a human mesothelial ce...

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Autores principales: Hillegass, Jedd M, Shukla, Arti, MacPherson, Maximilian B, Lathrop, Sherrill A, Alexeeva, Vlada, Perkins, Timothy N, van der Vliet, Albert, Vacek, Pamela M, Gunter, Mickey E, Mossman, Brooke T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945990/
https://www.ncbi.nlm.nih.gov/pubmed/20831825
http://dx.doi.org/10.1186/1743-8977-7-26
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author Hillegass, Jedd M
Shukla, Arti
MacPherson, Maximilian B
Lathrop, Sherrill A
Alexeeva, Vlada
Perkins, Timothy N
van der Vliet, Albert
Vacek, Pamela M
Gunter, Mickey E
Mossman, Brooke T
author_facet Hillegass, Jedd M
Shukla, Arti
MacPherson, Maximilian B
Lathrop, Sherrill A
Alexeeva, Vlada
Perkins, Timothy N
van der Vliet, Albert
Vacek, Pamela M
Gunter, Mickey E
Mossman, Brooke T
author_sort Hillegass, Jedd M
collection PubMed
description BACKGROUND: Exposures to an amphibole fiber in Libby, Montana cause increases in malignant mesothelioma (MM), a tumor of the pleural and peritoneal cavities with a poor prognosis. Affymetrix microarray/GeneSifter analysis was used to determine alterations in gene expression of a human mesothelial cell line (LP9/TERT-1) by a non-toxic concentration (15×10(6 )μm(2)/cm(2)) of unprocessed Libby six-mix and negative (glass beads) and positive (crocidolite asbestos) controls. Because manganese superoxide dismutase (MnSOD; SOD2) was the only gene upregulated significantly (p < 0.05) at both 8 and 24 h, we measured SOD protein and activity, oxidative stress and glutathione (GSH) levels to better understand oxidative events after exposure to non-toxic (15×10(6 )μm(2)/cm(2)) and toxic concentrations (75×10(6 )μm(2)/cm(2)) of Libby six-mix. RESULTS: Exposure to 15×10(6 )μm(2)/cm(2 )Libby six-mix elicited significant (p < 0.05) upregulation of one gene (SOD2; 4-fold) at 8 h and 111 gene changes at 24 h, including a 5-fold increase in SOD2. Increased levels of SOD2 mRNA at 24 h were also confirmed in HKNM-2 normal human pleural mesothelial cells by qRT-PCR. SOD2 protein levels were increased at toxic concentrations (75×10(6 )μm(2)/cm(2)) of Libby six-mix at 24 h. In addition, levels of copper-zinc superoxide dismutase (Cu/ZnSOD; SOD1) protein were increased at 24 h in all mineral groups. A dose-related increase in SOD2 activity was observed, although total SOD activity remained unchanged. Dichlorodihydrofluorescein diacetate (DCFDA) fluorescence staining and flow cytometry revealed a dose- and time-dependent increase in reactive oxygen species (ROS) production by LP9/TERT-1 cells exposed to Libby six-mix. Both Libby six-mix and crocidolite asbestos at 75×10(6 )μm(2)/cm(2 )caused transient decreases (p < 0.05) in GSH for up to 24 h and increases in gene expression of heme oxygenase 1 (HO-1) in LP9/TERT-1 and HKNM-2 cells. CONCLUSIONS: Libby six-mix causes multiple gene expression changes in LP9/TERT-1 human mesothelial cells, as well as increases in SOD2, increased production of oxidants, and transient decreases in intracellular GSH. These events are not observed at equal surface area concentrations of nontoxic glass beads. Results support a mechanistic basis for the importance of SOD2 in proliferation and apoptosis of mesothelial cells and its potential use as a biomarker of early responses to mesotheliomagenic minerals.
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spelling pubmed-29459902010-09-28 Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells Hillegass, Jedd M Shukla, Arti MacPherson, Maximilian B Lathrop, Sherrill A Alexeeva, Vlada Perkins, Timothy N van der Vliet, Albert Vacek, Pamela M Gunter, Mickey E Mossman, Brooke T Part Fibre Toxicol Research BACKGROUND: Exposures to an amphibole fiber in Libby, Montana cause increases in malignant mesothelioma (MM), a tumor of the pleural and peritoneal cavities with a poor prognosis. Affymetrix microarray/GeneSifter analysis was used to determine alterations in gene expression of a human mesothelial cell line (LP9/TERT-1) by a non-toxic concentration (15×10(6 )μm(2)/cm(2)) of unprocessed Libby six-mix and negative (glass beads) and positive (crocidolite asbestos) controls. Because manganese superoxide dismutase (MnSOD; SOD2) was the only gene upregulated significantly (p < 0.05) at both 8 and 24 h, we measured SOD protein and activity, oxidative stress and glutathione (GSH) levels to better understand oxidative events after exposure to non-toxic (15×10(6 )μm(2)/cm(2)) and toxic concentrations (75×10(6 )μm(2)/cm(2)) of Libby six-mix. RESULTS: Exposure to 15×10(6 )μm(2)/cm(2 )Libby six-mix elicited significant (p < 0.05) upregulation of one gene (SOD2; 4-fold) at 8 h and 111 gene changes at 24 h, including a 5-fold increase in SOD2. Increased levels of SOD2 mRNA at 24 h were also confirmed in HKNM-2 normal human pleural mesothelial cells by qRT-PCR. SOD2 protein levels were increased at toxic concentrations (75×10(6 )μm(2)/cm(2)) of Libby six-mix at 24 h. In addition, levels of copper-zinc superoxide dismutase (Cu/ZnSOD; SOD1) protein were increased at 24 h in all mineral groups. A dose-related increase in SOD2 activity was observed, although total SOD activity remained unchanged. Dichlorodihydrofluorescein diacetate (DCFDA) fluorescence staining and flow cytometry revealed a dose- and time-dependent increase in reactive oxygen species (ROS) production by LP9/TERT-1 cells exposed to Libby six-mix. Both Libby six-mix and crocidolite asbestos at 75×10(6 )μm(2)/cm(2 )caused transient decreases (p < 0.05) in GSH for up to 24 h and increases in gene expression of heme oxygenase 1 (HO-1) in LP9/TERT-1 and HKNM-2 cells. CONCLUSIONS: Libby six-mix causes multiple gene expression changes in LP9/TERT-1 human mesothelial cells, as well as increases in SOD2, increased production of oxidants, and transient decreases in intracellular GSH. These events are not observed at equal surface area concentrations of nontoxic glass beads. Results support a mechanistic basis for the importance of SOD2 in proliferation and apoptosis of mesothelial cells and its potential use as a biomarker of early responses to mesotheliomagenic minerals. BioMed Central 2010-09-11 /pmc/articles/PMC2945990/ /pubmed/20831825 http://dx.doi.org/10.1186/1743-8977-7-26 Text en Copyright ©2010 Hillegass et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hillegass, Jedd M
Shukla, Arti
MacPherson, Maximilian B
Lathrop, Sherrill A
Alexeeva, Vlada
Perkins, Timothy N
van der Vliet, Albert
Vacek, Pamela M
Gunter, Mickey E
Mossman, Brooke T
Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells
title Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells
title_full Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells
title_fullStr Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells
title_full_unstemmed Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells
title_short Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cells
title_sort mechanisms of oxidative stress and alterations in gene expression by libby six-mix in human mesothelial cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945990/
https://www.ncbi.nlm.nih.gov/pubmed/20831825
http://dx.doi.org/10.1186/1743-8977-7-26
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