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Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells
The evaluation of the toxicity of magnetic nanoparticles (MNPs) has attracted much attention in recent years. The current study aimed to investigate the cytotoxic effects of Fe(3)O(4), oleic acid-coated Fe(3)O(4 )(OA-Fe(3)O(4)), and carbon-coated Fe (C-Fe) nanoparticles on human hepatoma BEL-7402 ce...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3211994/ https://www.ncbi.nlm.nih.gov/pubmed/21801413 http://dx.doi.org/10.1186/1556-276X-6-480 |
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author | Kai, Wei Xiaojun, Xu Ximing, Pu Zhenqing, Hou Qiqing, Zhang |
author_facet | Kai, Wei Xiaojun, Xu Ximing, Pu Zhenqing, Hou Qiqing, Zhang |
author_sort | Kai, Wei |
collection | PubMed |
description | The evaluation of the toxicity of magnetic nanoparticles (MNPs) has attracted much attention in recent years. The current study aimed to investigate the cytotoxic effects of Fe(3)O(4), oleic acid-coated Fe(3)O(4 )(OA-Fe(3)O(4)), and carbon-coated Fe (C-Fe) nanoparticles on human hepatoma BEL-7402 cells and the mechanisms. WST-1 assay demonstrated that the cytotoxicity of three types of MNPs was in a dose-dependent manner. G1 (Fe(3)O(4 )and OA-Fe(3)O(4)) phase and G2 (C-Fe) phase cell arrests and apoptosis induced by MNPs were detected by flow cytometry analysis. The increase in apoptosis was accompanied with the Bax over-expression, mitochondrial membrane potential decrease, and the release of cytochrome C from mitochondria into cytosol. Moreover, apoptosis was further confirmed by morphological and biochemical hallmarks, such as swollen mitochondria with lysing cristae and caspase-3 activation. Our results revealed that certain concentrations of the three types of MNPs affect BEL-7402 cells viability via cell arrest and inducing apoptosis, and the MNPs-induced apoptosis is mediated through the mitochondrial-dependent pathway. The influence potency of MNPs observed in all experiments would be: C-Fe > Fe(3)O(4 )> OA-Fe(3)O(4). |
format | Online Article Text |
id | pubmed-3211994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer |
record_format | MEDLINE/PubMed |
spelling | pubmed-32119942011-11-09 Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells Kai, Wei Xiaojun, Xu Ximing, Pu Zhenqing, Hou Qiqing, Zhang Nanoscale Res Lett Nano Express The evaluation of the toxicity of magnetic nanoparticles (MNPs) has attracted much attention in recent years. The current study aimed to investigate the cytotoxic effects of Fe(3)O(4), oleic acid-coated Fe(3)O(4 )(OA-Fe(3)O(4)), and carbon-coated Fe (C-Fe) nanoparticles on human hepatoma BEL-7402 cells and the mechanisms. WST-1 assay demonstrated that the cytotoxicity of three types of MNPs was in a dose-dependent manner. G1 (Fe(3)O(4 )and OA-Fe(3)O(4)) phase and G2 (C-Fe) phase cell arrests and apoptosis induced by MNPs were detected by flow cytometry analysis. The increase in apoptosis was accompanied with the Bax over-expression, mitochondrial membrane potential decrease, and the release of cytochrome C from mitochondria into cytosol. Moreover, apoptosis was further confirmed by morphological and biochemical hallmarks, such as swollen mitochondria with lysing cristae and caspase-3 activation. Our results revealed that certain concentrations of the three types of MNPs affect BEL-7402 cells viability via cell arrest and inducing apoptosis, and the MNPs-induced apoptosis is mediated through the mitochondrial-dependent pathway. The influence potency of MNPs observed in all experiments would be: C-Fe > Fe(3)O(4 )> OA-Fe(3)O(4). Springer 2011-07-29 /pmc/articles/PMC3211994/ /pubmed/21801413 http://dx.doi.org/10.1186/1556-276X-6-480 Text en Copyright ©2011 Kai et al; licensee Springer. 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 | Nano Express Kai, Wei Xiaojun, Xu Ximing, Pu Zhenqing, Hou Qiqing, Zhang Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells |
title | Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells |
title_full | Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells |
title_fullStr | Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells |
title_full_unstemmed | Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells |
title_short | Cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma BEL-7402 cells |
title_sort | cytotoxic effects and the mechanism of three types of magnetic nanoparticles on human hepatoma bel-7402 cells |
topic | Nano Express |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3211994/ https://www.ncbi.nlm.nih.gov/pubmed/21801413 http://dx.doi.org/10.1186/1556-276X-6-480 |
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