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Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions

OBJECTIVES: The cytotoxicity induced by cobalt ions (Co(2+)) and cobalt nanoparticles (Co-NPs) which released following the insertion of a total hip prosthesis, has been reported. However, little is known about the underlying mechanisms. In this study, we investigate the toxic effect of Co(2+) and C...

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Autores principales: Liu, Y. K., Deng, X. X., Yang, H.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075796/
https://www.ncbi.nlm.nih.gov/pubmed/27754833
http://dx.doi.org/10.1302/2046-3758.510.BJR-2016-0016.R1
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author Liu, Y. K.
Deng, X. X.
Yang, H.L.
author_facet Liu, Y. K.
Deng, X. X.
Yang, H.L.
author_sort Liu, Y. K.
collection PubMed
description OBJECTIVES: The cytotoxicity induced by cobalt ions (Co(2+)) and cobalt nanoparticles (Co-NPs) which released following the insertion of a total hip prosthesis, has been reported. However, little is known about the underlying mechanisms. In this study, we investigate the toxic effect of Co(2+) and Co-NPs on liver cells, and explain further the potential mechanisms. METHODS: Co-NPs were characterised for size, shape, elemental analysis, and hydrodynamic diameter, and were assessed by Transmission Electron Microscope, Scanning Electron Microscope, Energy Dispersive X-ray Spectroscopy and Dynamic Light Scattering. BRL-3A cells were used in this study. Cytotoxicity was evaluated by MTT and lactate dehydrogenase release assay. In order to clarify the potential mechanisms, reactive oxygen species, Bax/Bcl-2 mRNA expression, IL-8 mRNA expression and DNA damage were assessed on BRL-3A cells after Co(2+) or Co-NPs treatment. RESULTS: Results showed cytotoxic effects of Co(2+) and Co-NPs were dependent upon time and dosage, and the cytotoxicity of Co-NPs was greater than that of Co(2+). In addition, Co-NPs elicited a significant (p < 0.05) reduction in cell viability with a concomitant increase in lactic dehydrogenase release, reactive oxygen species generation, IL-8 mRNA expression, Bax/Bcl-2 mRNA expression and DNA damage after 24 hours of exposure. CONCLUSION: Co-NPs induced greater cytotoxicity and genotoxicity in BRL-3A cells than Co(2+). Cell membrane damage, oxidative stress, immune inflammation and DNA damage may play an important role in the effects of Co-NPs on liver cells. Cite this article: Y. K. Liu, X. X. Deng, H.L. Yang. Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions. Bone Joint Res 2016;5:461–469. DOI: 10.1302/2046-3758.510.BJR-2016-0016.R1.
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spelling pubmed-50757962016-11-08 Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions Liu, Y. K. Deng, X. X. Yang, H.L. Bone Joint Res Research OBJECTIVES: The cytotoxicity induced by cobalt ions (Co(2+)) and cobalt nanoparticles (Co-NPs) which released following the insertion of a total hip prosthesis, has been reported. However, little is known about the underlying mechanisms. In this study, we investigate the toxic effect of Co(2+) and Co-NPs on liver cells, and explain further the potential mechanisms. METHODS: Co-NPs were characterised for size, shape, elemental analysis, and hydrodynamic diameter, and were assessed by Transmission Electron Microscope, Scanning Electron Microscope, Energy Dispersive X-ray Spectroscopy and Dynamic Light Scattering. BRL-3A cells were used in this study. Cytotoxicity was evaluated by MTT and lactate dehydrogenase release assay. In order to clarify the potential mechanisms, reactive oxygen species, Bax/Bcl-2 mRNA expression, IL-8 mRNA expression and DNA damage were assessed on BRL-3A cells after Co(2+) or Co-NPs treatment. RESULTS: Results showed cytotoxic effects of Co(2+) and Co-NPs were dependent upon time and dosage, and the cytotoxicity of Co-NPs was greater than that of Co(2+). In addition, Co-NPs elicited a significant (p < 0.05) reduction in cell viability with a concomitant increase in lactic dehydrogenase release, reactive oxygen species generation, IL-8 mRNA expression, Bax/Bcl-2 mRNA expression and DNA damage after 24 hours of exposure. CONCLUSION: Co-NPs induced greater cytotoxicity and genotoxicity in BRL-3A cells than Co(2+). Cell membrane damage, oxidative stress, immune inflammation and DNA damage may play an important role in the effects of Co-NPs on liver cells. Cite this article: Y. K. Liu, X. X. Deng, H.L. Yang. Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions. Bone Joint Res 2016;5:461–469. DOI: 10.1302/2046-3758.510.BJR-2016-0016.R1. 2016-10-18 /pmc/articles/PMC5075796/ /pubmed/27754833 http://dx.doi.org/10.1302/2046-3758.510.BJR-2016-0016.R1 Text en © 2016 Yang et al. This is an open-access article distributed under the terms of the Creative Commons Attributions licence (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
spellingShingle Research
Liu, Y. K.
Deng, X. X.
Yang, H.L.
Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions
title Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions
title_full Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions
title_fullStr Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions
title_full_unstemmed Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions
title_short Cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions
title_sort cytotoxicity and genotoxicity in liver cells induced by cobalt nanoparticles and ions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075796/
https://www.ncbi.nlm.nih.gov/pubmed/27754833
http://dx.doi.org/10.1302/2046-3758.510.BJR-2016-0016.R1
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