Cargando…

Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells

Magnetic Fe(3)O(4) nanoparticles (Fe(3)O(4)-NPs) have been widely investigated for their biomedical applications. The main purpose of this study was to evaluate the cytotoxic effects of different sizes of Fe(3)O(4)-NPs in chicken macrophage cells (HD11). Experimental groups based on three sizes of F...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Shan, Wu, Shu, Shen, Yiru, Xiao, Yunqi, Gao, Lizeng, Shi, Shourong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211854/
https://www.ncbi.nlm.nih.gov/pubmed/32431865
http://dx.doi.org/10.1098/rsos.191561
_version_ 1783531526462373888
author Zhang, Shan
Wu, Shu
Shen, Yiru
Xiao, Yunqi
Gao, Lizeng
Shi, Shourong
author_facet Zhang, Shan
Wu, Shu
Shen, Yiru
Xiao, Yunqi
Gao, Lizeng
Shi, Shourong
author_sort Zhang, Shan
collection PubMed
description Magnetic Fe(3)O(4) nanoparticles (Fe(3)O(4)-NPs) have been widely investigated for their biomedical applications. The main purpose of this study was to evaluate the cytotoxic effects of different sizes of Fe(3)O(4)-NPs in chicken macrophage cells (HD11). Experimental groups based on three sizes of Fe(3)O(4)-NPs (60, 120 and 250 nm) were created, and the Fe(3)O(4)-NPs were added to the cells at different doses according to the experimental group. The cell activity, oxidative index (malondialdehyde (MDA), superoxide dismutase (SOD) and reactive oxygen species (ROS)), apoptosis and pro-inflammatory cytokine secretion level were detected to analyse the cytotoxic effects of Fe(3)O(4)-NPs of different sizes in HD11 cells. The results revealed that the cell viability of the 60 nm Fe(3)O(4)-NPs group was lower than those of the 120 and 250 nm groups when the same concentration of Fe(3)O(4)-NPs was added. No significant difference in MDA was observed among the three Fe(3)O(4)-NP groups. The SOD level and ROS production of the 60 nm group were significantly greater than those of the 120 and 250 nm groups. Furthermore, the highest levels of apoptosis and pro-inflammatory cytokine secretion were caused by the 60 nm Fe(3)O(4)-NPs. In conclusion, the smaller Fe(3)O(4)-NPs produced stronger cytotoxicity in chicken macrophage cells, and the cytotoxic effects may be related to the oxidative stress and apoptosis induced by increased ROS production as well as the increased expression of pro-inflammatory cytokines.
format Online
Article
Text
id pubmed-7211854
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-72118542020-05-19 Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells Zhang, Shan Wu, Shu Shen, Yiru Xiao, Yunqi Gao, Lizeng Shi, Shourong R Soc Open Sci Chemistry Magnetic Fe(3)O(4) nanoparticles (Fe(3)O(4)-NPs) have been widely investigated for their biomedical applications. The main purpose of this study was to evaluate the cytotoxic effects of different sizes of Fe(3)O(4)-NPs in chicken macrophage cells (HD11). Experimental groups based on three sizes of Fe(3)O(4)-NPs (60, 120 and 250 nm) were created, and the Fe(3)O(4)-NPs were added to the cells at different doses according to the experimental group. The cell activity, oxidative index (malondialdehyde (MDA), superoxide dismutase (SOD) and reactive oxygen species (ROS)), apoptosis and pro-inflammatory cytokine secretion level were detected to analyse the cytotoxic effects of Fe(3)O(4)-NPs of different sizes in HD11 cells. The results revealed that the cell viability of the 60 nm Fe(3)O(4)-NPs group was lower than those of the 120 and 250 nm groups when the same concentration of Fe(3)O(4)-NPs was added. No significant difference in MDA was observed among the three Fe(3)O(4)-NP groups. The SOD level and ROS production of the 60 nm group were significantly greater than those of the 120 and 250 nm groups. Furthermore, the highest levels of apoptosis and pro-inflammatory cytokine secretion were caused by the 60 nm Fe(3)O(4)-NPs. In conclusion, the smaller Fe(3)O(4)-NPs produced stronger cytotoxicity in chicken macrophage cells, and the cytotoxic effects may be related to the oxidative stress and apoptosis induced by increased ROS production as well as the increased expression of pro-inflammatory cytokines. The Royal Society 2020-04-08 /pmc/articles/PMC7211854/ /pubmed/32431865 http://dx.doi.org/10.1098/rsos.191561 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Chemistry
Zhang, Shan
Wu, Shu
Shen, Yiru
Xiao, Yunqi
Gao, Lizeng
Shi, Shourong
Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells
title Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells
title_full Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells
title_fullStr Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells
title_full_unstemmed Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells
title_short Cytotoxicity studies of Fe(3)O(4) nanoparticles in chicken macrophage cells
title_sort cytotoxicity studies of fe(3)o(4) nanoparticles in chicken macrophage cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211854/
https://www.ncbi.nlm.nih.gov/pubmed/32431865
http://dx.doi.org/10.1098/rsos.191561
work_keys_str_mv AT zhangshan cytotoxicitystudiesoffe3o4nanoparticlesinchickenmacrophagecells
AT wushu cytotoxicitystudiesoffe3o4nanoparticlesinchickenmacrophagecells
AT shenyiru cytotoxicitystudiesoffe3o4nanoparticlesinchickenmacrophagecells
AT xiaoyunqi cytotoxicitystudiesoffe3o4nanoparticlesinchickenmacrophagecells
AT gaolizeng cytotoxicitystudiesoffe3o4nanoparticlesinchickenmacrophagecells
AT shishourong cytotoxicitystudiesoffe3o4nanoparticlesinchickenmacrophagecells