Cytotoxic and Genotoxic Effects of Silver Nanoparticles on Primary Syrian Hamster Embryo (SHE) Cells

被引:0
作者
Li, Xuefei [1 ,2 ]
Xu, Liming [1 ,2 ]
Shao, Anliang [1 ]
Wu, Gang [2 ]
Hanagata, Nobutaka [3 ]
机构
[1] Natl Inst Food & Drug Control, Inst Med Devices Control, Beijing 100050, Peoples R China
[2] Inner Mongolia Univ Sci & Technol, Baotou Med Coll, Baotou 014010, Peoples R China
[3] Natl Inst Mat Sci, Interdisciplinary Lab Nanoscale Sci & Technol, Tsukuba, Ibaraki 3050047, Japan
基金
北京市自然科学基金;
关键词
Silver-NPs; Primary Syrian Hamster Embryo (SHE) Cells; Cytotoxicity; Genotoxicity; Cell Cycles; Apoptosis; OXIDATIVE STRESS; TOXICITY; NANOMATERIALS; NANOSILVER; TOXICOLOGY; EXPRESSION; BRAIN;
D O I
10.1166/jnn.2013.7077
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Silver-nanoparticles (NPs) have become increasingly common in various applications, raising some safety concerns. In this study, the cytotoxic and genotoxic effects of silver-NPs on primary Syrian hamster embryo (SHE) cells were investigated. Cell viability was assessed using a methyl tetrazolium (MTT) assay, and genotoxic potential was evaluated using a cytokinesis-block micronucleus (CBMN) assay. The results showed that dose-dependent cytotoxicity was induced after 24 h of exposure to silver-NPs. The micronucleation frequency (MNF) also increased significantly in a dose-dependent manner (P < 0.05), suggesting that silver-NPs induce genotoxicity. This is consistent with an increased MNF observed in primary SHE cells. The results of cell cycle analysis indicate that the cell cycles became arrested in the G0/G1 phase and that the S phase shortened after only 8 h of silver-NP exposure, suggesting that DNA replication had been inhibited, which in turn inhibited further cell proliferation. The rate of late-stage apoptosis increased after 12 h of silver-NP exposure, and both early- and late-stage apoptosis were obviously increased after 72 h of exposure than in controls. This study demonstrated that silver-NPs could induce strong cytotoxicity and significant genotoxicity in primary SHE cells and that this is probably due to silver-NP-induced apoptosis and the inhibition of cell proliferation.
引用
收藏
页码:161 / 170
页数:10
相关论文
共 37 条
[1]   Silver nanoparticle applications and human health [J].
Ahamed, Maqusood ;
AlSalhi, Mohamad S. ;
Siddiqui, M. K. J. .
CLINICA CHIMICA ACTA, 2010, 411 (23-24) :1841-1848
[2]   Anti-proliferative activity of silver nanoparticles [J].
AshaRani, P. V. ;
Hande, M. Prakash ;
Valiyaveettil, Suresh .
BMC CELL BIOLOGY, 2009, 10 :65
[3]   Cytotoxicity and Genotoxicity of Silver Nanoparticles in Human Cells [J].
AshaRani, P. V. ;
Mun, Grace Low Kah ;
Hande, Manoor Prakash ;
Valiyaveettil, Suresh .
ACS NANO, 2009, 3 (02) :279-290
[4]   The carcinogenic potential of nanomaterials, their release from products and options for regulating them [J].
Becker, Heidi ;
Herzberg, Frank ;
Schulte, Agnes ;
Kolossa-Gehring, Marike .
INTERNATIONAL JOURNAL OF HYGIENE AND ENVIRONMENTAL HEALTH, 2011, 214 (03) :231-238
[5]   Unique Cellular Interaction of Silver Nanoparticles: Size-Dependent Generation of Reactive Oxygen Species [J].
Carlson, C. ;
Hussain, S. M. ;
Schrand, A. M. ;
Braydich-Stolle, L. K. ;
Hess, K. L. ;
Jones, R. L. ;
Schlager, J. J. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (43) :13608-13619
[6]   Nanosilver as a new generation of nanoproduct in biomedical applications [J].
Chaloupka, Karla ;
Malam, Yogeshkumar ;
Seifalian, Alexander M. .
TRENDS IN BIOTECHNOLOGY, 2010, 28 (11) :580-588
[7]   Nanosilver: A nanoproduct in medical application [J].
Chen, X. ;
Schluesener, H. J. .
TOXICOLOGY LETTERS, 2008, 176 (01) :1-12
[8]  
Dong Z, 2012, CHI J PHARM ANAL, V2, P33
[9]   Surface Charge-Dependent Toxicity of Silver Nanoparticles [J].
El Badawy, Amro M. ;
Silva, Rendahandi G. ;
Morris, Brian ;
Scheckel, Kirk G. ;
Suidan, Makram T. ;
Tolaymat, Thabet M. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2011, 45 (01) :283-287
[10]   The in vitro micronucleus technique [J].
Fenech, M .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2000, 455 (1-2) :81-95