The influence of the surface chemistry of silver nanoparticles on cell death

被引:72
作者
Sur, Ilknur [1 ]
Altunbek, Mine [1 ]
Kahraman, Mehmet [1 ]
Culha, Mustafa [1 ]
机构
[1] Yeditepe Univ, Fac Engn, Dept Genet & Bioengn, TR-34755 Istanbul, Turkey
关键词
DNA-DAMAGE; CANCER-CELLS; ENHANCED RAMAN; GOLD NANOPARTICLES; INDUCED APOPTOSIS; HUMAN SKIN; CYTOTOXICITY; TOXICITY; P53; SIZE;
D O I
10.1088/0957-4484/23/37/375102
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
The influence of the surface chemistry of silver nanoparticles (AgNPs) on p53 mediated cell death was evaluated using human dermal fibroblast (HDF) and lung cancer (A549) cells. The citrate reduced AgNPs (C-AgNPs) were modified with either lactose (L-AgNPs) or a 12-base long oligonucleotide (O-AgNPs). Both unmodified and modified AgNPs showed increased concentration and time dependent cytotoxicity and genotoxicity causing an increased p53 up-regulation within 6 h and led to apoptotic or necrotic cell deaths. The C-AgNPs induced more cytotoxicity and cellular DNA damage than the surface modified AgNPs. Modifying the C-AgNPs with lactose or the oligonucleotide reduced both necrotic and apoptotic cell deaths in the HDF cells. The C-AgNPs caused an insignificant necrosis in A549 cells whereas the modified AgNPs caused necrosis and apoptosis in both cell types. Compared to the O-AgNPs, the L-AgNPs triggered more cellular DNA damage, which led to up-regulation of p53 gene inducing apoptosis in A549 cells compared to HDF cells. This suggests that the different surface chemistries of the AgNPs cause different cellular responses that may be important not only for their use in medicine but also for reducing their toxicity.
引用
收藏
页数:12
相关论文
共 61 条
[1]
Genotoxic potential of copper oxide nanoparticles in human lung epithelial cells [J].
Ahamed, Maqusood ;
Siddiqui, Maqsood A. ;
Akhtar, Mohd J. ;
Ahmad, Iqbal ;
Pant, Aditya B. ;
Alhadlaq, Hisham A. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 396 (02) :578-583
[2]
DNA damage response to different surface chemistry of silver nanoparticles in mammalian cells [J].
Ahamed, Maqusood ;
Karns, Michael ;
Goodson, Michael ;
Rowe, John ;
Hussain, Saber M. ;
Schlager, John J. ;
Hong, Yiling .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2008, 233 (03) :404-410
[3]
Role of nanoparticle surface charge in surface-enhanced Raman scattering [J].
Alvarez-Puebla, RA ;
Arceo, E ;
Goulet, PJG ;
Garrido, JJ ;
Aroca, RF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (09) :3787-3792
[4]
[Anonymous], 1924, Biochem Z
[5]
Asharani PV, 2010, NANOMEDICINE-UK, V5, P51, DOI [10.2217/nnm.09.85, 10.2217/NNM.09.85]
[6]
Toxicity of silver nanoparticles in zebrafish models [J].
Asharani, P. V. ;
Wu, Yi Lian ;
Gong, Zhiyuan ;
Valiyaveettil, Suresh .
NANOTECHNOLOGY, 2008, 19 (25)
[7]
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
[8]
CeO2 nanoparticles induce DNA damage towards human dermal fibroblasts in vitro [J].
Auffan, Melanie ;
Rose, Jerome ;
Orsiere, Thierry ;
De Meo, Michel ;
Thill, Antoine ;
Zeyons, Ophelie ;
Proux, Olivier ;
Masion, Armand ;
Chaurand, Perrine ;
Spalla, Olivier ;
Botta, Alain ;
Wiesner, Mark R. ;
Bottero, Jean-Yves .
NANOTOXICOLOGY, 2009, 3 (02) :161-U115
[9]
DEVIANT ENERGETIC METABOLISM OF GLYCOLYTIC CANCER-CELLS [J].
BAGGETTO, LG .
BIOCHIMIE, 1992, 74 (11) :959-974
[10]
Cytotoxicity of peptide-coated silver nanoparticles on the human intestinal cell line Caco-2 [J].
Boehmert, Linda ;
Niemann, Birgit ;
Thuenemann, Andreas F. ;
Lampen, Alfonso .
ARCHIVES OF TOXICOLOGY, 2012, 86 (07) :1107-1115