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Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling

Silver nanoparticles (AgNPs) are widely used nanoparticles and they are mainly used in antibacterial and personal care products. In this study, we evaluated the effect of AgNPs on cell death induction in the murine dendritic cell line DC2.4. DC2.4 cells exposed to AgNPs showed a marked decrease in c...

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Detalles Bibliográficos
Autores principales: Kang, Kyeongah, Jung, Hyeyoun, Lim, Jong-Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762268/
https://www.ncbi.nlm.nih.gov/pubmed/24009827
http://dx.doi.org/10.4062/biomolther.2012.20.4.399
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author Kang, Kyeongah
Jung, Hyeyoun
Lim, Jong-Seok
author_facet Kang, Kyeongah
Jung, Hyeyoun
Lim, Jong-Seok
author_sort Kang, Kyeongah
collection PubMed
description Silver nanoparticles (AgNPs) are widely used nanoparticles and they are mainly used in antibacterial and personal care products. In this study, we evaluated the effect of AgNPs on cell death induction in the murine dendritic cell line DC2.4. DC2.4 cells exposed to AgNPs showed a marked decrease in cell viability and an induction of lactate dehydrogenase (LDH) leakage in a time- and dose-dependent manner. In addition, AgNPs promoted reactive oxygen species (ROS)-dependent apoptosis and AgNP-induced ROS triggered a decrease in mitochondrial membrane potential. The activation of the intracellular signal transduction pathway was also observed in cells cultured with AgNPs. Taken together, our data demonstrate that AgNPs are able to induce a cytotoxic effect in DCs through ROS generation. This study provides important information about the safety of AgNPs that may help in guiding the development of nanotechnology applications.
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spelling pubmed-37622682013-09-05 Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling Kang, Kyeongah Jung, Hyeyoun Lim, Jong-Seok Biomol Ther (Seoul) Articles Silver nanoparticles (AgNPs) are widely used nanoparticles and they are mainly used in antibacterial and personal care products. In this study, we evaluated the effect of AgNPs on cell death induction in the murine dendritic cell line DC2.4. DC2.4 cells exposed to AgNPs showed a marked decrease in cell viability and an induction of lactate dehydrogenase (LDH) leakage in a time- and dose-dependent manner. In addition, AgNPs promoted reactive oxygen species (ROS)-dependent apoptosis and AgNP-induced ROS triggered a decrease in mitochondrial membrane potential. The activation of the intracellular signal transduction pathway was also observed in cells cultured with AgNPs. Taken together, our data demonstrate that AgNPs are able to induce a cytotoxic effect in DCs through ROS generation. This study provides important information about the safety of AgNPs that may help in guiding the development of nanotechnology applications. The Korean Society of Applied Pharmacology 2012-07 /pmc/articles/PMC3762268/ /pubmed/24009827 http://dx.doi.org/10.4062/biomolther.2012.20.4.399 Text en Copyright ©2012, The Korean Society of Pharmaceutics
spellingShingle Articles
Kang, Kyeongah
Jung, Hyeyoun
Lim, Jong-Seok
Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling
title Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling
title_full Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling
title_fullStr Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling
title_full_unstemmed Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling
title_short Cell Death by Polyvinylpyrrolidine-Coated Silver Nanoparticles is Mediated by ROS-Dependent Signaling
title_sort cell death by polyvinylpyrrolidine-coated silver nanoparticles is mediated by ros-dependent signaling
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762268/
https://www.ncbi.nlm.nih.gov/pubmed/24009827
http://dx.doi.org/10.4062/biomolther.2012.20.4.399
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