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Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment

BACKGROUND: Rapid increase in multi-walled carbon nanotube (MWCNT) production for their industrial and biomedical applications has led to concerns over the effects of MWCNTs on human health and the environment. Both animal and in vitro studies have provided important findings about MWCNT-induced eff...

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Autores principales: Patel, Hemang, Kwon, Soonjo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552678/
https://www.ncbi.nlm.nih.gov/pubmed/23148460
http://dx.doi.org/10.1186/1754-1611-6-22
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author Patel, Hemang
Kwon, Soonjo
author_facet Patel, Hemang
Kwon, Soonjo
author_sort Patel, Hemang
collection PubMed
description BACKGROUND: Rapid increase in multi-walled carbon nanotube (MWCNT) production for their industrial and biomedical applications has led to concerns over the effects of MWCNTs on human health and the environment. Both animal and in vitro studies have provided important findings about MWCNT-induced effects on the lung cells or tissues. In vitro studies have provided a considerable amount of fundamental information on MWCNT-induced effects on the specific lung cells. However, the cell culture systems used in those studies were limited by the absence of dynamic nature of lung tissues. We hypothesized that MWCNT-induced cellular responses such as proliferation, inflammation, and oxidative stress under dynamic cell growth environment may differ from those under static cell growth environment. RESULTS: In this study, we used a dynamic cell growth condition to mimic mechanically dynamic environment of the lung and characterized interleukin 8 (IL-8), reactive oxygen species (ROS), glutathione (GSH), and cell proliferation for three days following exposure of MWCNTs at different concentrations (5, 10, and 20 μg/ml) to A549 cell monolayer under both static and dynamic cell growth conditions. Our results demonstrated the distinct differences in the levels of inflammatory response and oxidative stress between static and dynamic cell growth conditions. CONCLUSIONS: In conclusion, the dynamic cell growth system used in this study provided important changes in cellular responses that were not found in the static cell growth system and were similar to animal studies. The dynamic cell growth system can be considered as a viable alternative to in vivo test system in combination with existing in vitro static cell growth systems to evaluate the effect of MWCNTs on cellular responses in the respiratory system.
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spelling pubmed-35526782013-01-28 Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment Patel, Hemang Kwon, Soonjo J Biol Eng Research BACKGROUND: Rapid increase in multi-walled carbon nanotube (MWCNT) production for their industrial and biomedical applications has led to concerns over the effects of MWCNTs on human health and the environment. Both animal and in vitro studies have provided important findings about MWCNT-induced effects on the lung cells or tissues. In vitro studies have provided a considerable amount of fundamental information on MWCNT-induced effects on the specific lung cells. However, the cell culture systems used in those studies were limited by the absence of dynamic nature of lung tissues. We hypothesized that MWCNT-induced cellular responses such as proliferation, inflammation, and oxidative stress under dynamic cell growth environment may differ from those under static cell growth environment. RESULTS: In this study, we used a dynamic cell growth condition to mimic mechanically dynamic environment of the lung and characterized interleukin 8 (IL-8), reactive oxygen species (ROS), glutathione (GSH), and cell proliferation for three days following exposure of MWCNTs at different concentrations (5, 10, and 20 μg/ml) to A549 cell monolayer under both static and dynamic cell growth conditions. Our results demonstrated the distinct differences in the levels of inflammatory response and oxidative stress between static and dynamic cell growth conditions. CONCLUSIONS: In conclusion, the dynamic cell growth system used in this study provided important changes in cellular responses that were not found in the static cell growth system and were similar to animal studies. The dynamic cell growth system can be considered as a viable alternative to in vivo test system in combination with existing in vitro static cell growth systems to evaluate the effect of MWCNTs on cellular responses in the respiratory system. BioMed Central 2012-11-13 /pmc/articles/PMC3552678/ /pubmed/23148460 http://dx.doi.org/10.1186/1754-1611-6-22 Text en Copyright ©2012 Patel and Kwon; 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
Patel, Hemang
Kwon, Soonjo
Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment
title Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment
title_full Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment
title_fullStr Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment
title_full_unstemmed Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment
title_short Multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment
title_sort multi-walled carbon nanotube-induced inflammatory response and oxidative stress in a dynamic cell growth environment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552678/
https://www.ncbi.nlm.nih.gov/pubmed/23148460
http://dx.doi.org/10.1186/1754-1611-6-22
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