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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,...

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Autores principales: Xu, Liming, Li, Xuefei, Takemura, Taro, Hanagata, Nobutaka, Wu, Gang, Chou, Laisheng Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
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.
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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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