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Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel
BACKGROUND: Since silver-nanoparticles (NPs) possess an antibacterial activity, they were commonly used in medical products and devices, food storage materials, cosmetics, various health care products, and industrial products. Various silver-NP based medical devices are available for clinical uses,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430588/ https://www.ncbi.nlm.nih.gov/pubmed/22548743 http://dx.doi.org/10.1186/1477-3155-10-16 |
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author | Xu, Liming Li, Xuefei Takemura, Taro Hanagata, Nobutaka Wu, Gang Chou, Laisheng Lee |
author_facet | Xu, Liming Li, Xuefei Takemura, Taro Hanagata, Nobutaka Wu, Gang Chou, Laisheng Lee |
author_sort | Xu, Liming |
collection | PubMed |
description | BACKGROUND: Since silver-nanoparticles (NPs) possess an antibacterial activity, they were commonly used in medical products and devices, food storage materials, cosmetics, various health care products, and industrial products. Various silver-NP based medical devices are available for clinical uses, such as silver-NP based dressing and silver-NP based hydrogel (silver-NP-hydrogel) for medical applications. Although the previous data have suggested silver-NPs induced toxicity in vivo and in vitro, there is lack information about the mechanisms of biological response and potential toxicity of silver-NP-hydrogel. METHODS: In this study, the genotoxicity of silver-NP-hydrogel was assayed using cytokinesis-block micronucleus (CBMN). The molecular response was studied using DNA microarray and GO pathway analysis. RESULTS AND DISCUSSION: The results of global gene expression analysis in HeLa cells showed that thousands of genes were up- or down-regulated at 48 h of silver-NP-hydrogel exposure. Further GO pathway analysis suggested that fourteen theoretical activating signaling pathways were attributed to up-regulated genes; and three signal pathways were attributed to down-regulated genes. It was discussed that the cells protect themselves against silver NP-mediated toxicity through up-regulating metallothionein genes and anti-oxidative stress genes. The changes in DNA damage, apoptosis and mitosis pathway were closely related to silver-NP-induced cytotoxicity and chromosome damage. The down-regulation of CDC14A via mitosis pathway might play a role in potential genotoxicity induced by silver-NPs. CONCLUSIONS: The silver-NP-hydrogel induced micronuclei formation in cellular level and broad spectrum molecular responses in gene expression level. The results of signal pathway analysis suggested that the balances between anti-ROS response and DNA damage, chromosome instability, mitosis inhibition might play important roles in silver-NP induced toxicity. The inflammatory factors were likely involved in silver-NP-hydrogel complex-induced toxic effects via JAK-STAT signal transduction pathway and immune response pathway. These biological responses eventually decide the future of the cells, survival or apoptosis. |
format | Online Article Text |
id | pubmed-3430588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34305882012-08-30 Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel Xu, Liming Li, Xuefei Takemura, Taro Hanagata, Nobutaka Wu, Gang Chou, Laisheng Lee J Nanobiotechnology Research BACKGROUND: Since silver-nanoparticles (NPs) possess an antibacterial activity, they were commonly used in medical products and devices, food storage materials, cosmetics, various health care products, and industrial products. Various silver-NP based medical devices are available for clinical uses, such as silver-NP based dressing and silver-NP based hydrogel (silver-NP-hydrogel) for medical applications. Although the previous data have suggested silver-NPs induced toxicity in vivo and in vitro, there is lack information about the mechanisms of biological response and potential toxicity of silver-NP-hydrogel. METHODS: In this study, the genotoxicity of silver-NP-hydrogel was assayed using cytokinesis-block micronucleus (CBMN). The molecular response was studied using DNA microarray and GO pathway analysis. RESULTS AND DISCUSSION: The results of global gene expression analysis in HeLa cells showed that thousands of genes were up- or down-regulated at 48 h of silver-NP-hydrogel exposure. Further GO pathway analysis suggested that fourteen theoretical activating signaling pathways were attributed to up-regulated genes; and three signal pathways were attributed to down-regulated genes. It was discussed that the cells protect themselves against silver NP-mediated toxicity through up-regulating metallothionein genes and anti-oxidative stress genes. The changes in DNA damage, apoptosis and mitosis pathway were closely related to silver-NP-induced cytotoxicity and chromosome damage. The down-regulation of CDC14A via mitosis pathway might play a role in potential genotoxicity induced by silver-NPs. CONCLUSIONS: The silver-NP-hydrogel induced micronuclei formation in cellular level and broad spectrum molecular responses in gene expression level. The results of signal pathway analysis suggested that the balances between anti-ROS response and DNA damage, chromosome instability, mitosis inhibition might play important roles in silver-NP induced toxicity. The inflammatory factors were likely involved in silver-NP-hydrogel complex-induced toxic effects via JAK-STAT signal transduction pathway and immune response pathway. These biological responses eventually decide the future of the cells, survival or apoptosis. BioMed Central 2012-05-01 /pmc/articles/PMC3430588/ /pubmed/22548743 http://dx.doi.org/10.1186/1477-3155-10-16 Text en Copyright ©2012 Xu 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 Xu, Liming Li, Xuefei Takemura, Taro Hanagata, Nobutaka Wu, Gang Chou, Laisheng Lee Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel |
title | Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel |
title_full | Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel |
title_fullStr | Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel |
title_full_unstemmed | Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel |
title_short | Genotoxicity and molecular response of silver nanoparticle (NP)-based hydrogel |
title_sort | genotoxicity and molecular response of silver nanoparticle (np)-based hydrogel |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430588/ https://www.ncbi.nlm.nih.gov/pubmed/22548743 http://dx.doi.org/10.1186/1477-3155-10-16 |
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