Size-dependent cellular toxicity of silver nanoparticles

被引:391
作者
Kim, Tae-Hyun
Kim, Meeju
Park, Hyung-Seok
Shin, Ueon Sang
Gong, Myoung-Seon
Kim, Hae-Won
机构
[1] Institute of Tissue Regeneration Engineering (ITREN), Dankook University
[2] Department of Nanobiomedical Science, WCU Research Center, Dankook University
[3] Department of Chemistry, Dankook University
[4] Department of Biomaterials Science, School of Dentistry, Dankook University
基金
新加坡国家研究基金会;
关键词
silver nanoparticles; cell toxicity; in vitro; size dependence; endocytosis; NUCLEAR-PORE COMPLEX; OXIDATIVE STRESS; INDUCED CYTOTOXICITY; GOLD NANOPARTICLES; ORAL TOXICITY; APOPTOSIS; MECHANISM; NANOSILVER; RESPONSES; EXPOSURE;
D O I
10.1002/jbm.a.34053
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Silver nanoparticles (AgNPs) have found a variety of uses including biomedical materials; however, studies of the cytotoxicity of AgNPs by size effects are only in the beginning stage. In this study, we examined the size-dependent cellular toxicity of AgNPs using three different characteristic sizes (similar to 10, 50, and 100 nm) against several cell lines including MC3T3-E1 and PC12. The cytotoxic effect determined based on the cell viability, intracellular reactive oxygen species generation, lactate dehydrogenase release, ultrastructural changes in cell morphology, and upregulation of stress-related genes (ho-1 and MMP-3) was fairly size- and dose-dependent. In particular, AgNPs stimulated apoptosis in the MC3T3-E1 cells, but induced necrotic cell death in the PC12 cells. Furthermore, the smallest sized AgNPs (10 nm size) had a greater ability to induce apoptosis in the MC3T3-E1 cells than the other sized AgNPs (50 and 100 nm). These data suggest that the AgNPs-induced cytotoxic effects against tissue cells are particle size-dependent, and thus, the particle size needs careful consideration in the design of the nanoparticles for biomedical uses. (C) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A:, 2012.
引用
收藏
页码:1033 / 1043
页数:11
相关论文
共 58 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]
Cellular responses induced by silver nanoparticles:: In vitro studies [J].
Arora, S. ;
Jain, J. ;
Rajwade, J. M. ;
Paknikar, K. M. .
TOXICOLOGY LETTERS, 2008, 179 (02) :93-100
[3]
Interactions of silver nanoparticles with primary mouse fibroblasts and liver cells [J].
Arora, S. ;
Jain, J. ;
Rajwade, J. M. ;
Paknikar, K. M. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2009, 236 (03) :310-318
[4]
Anti-proliferative activity of silver nanoparticles [J].
AshaRani, P. V. ;
Hande, M. Prakash ;
Valiyaveettil, Suresh .
BMC CELL BIOLOGY, 2009, 10 :65
[5]
Intravesical nanocrystalline silver decreases experimental bladder inflammation [J].
Boucher, W. ;
Stern, J. M. ;
Kotsinyan, V. ;
Kempuraj, D. ;
Papaliodis, D. ;
Cohen, M. S. ;
Theoharides, T. C. .
JOURNAL OF UROLOGY, 2008, 179 (04) :1598-1602
[6]
Role of poly(ADP-ribose) polymerase (PARP) cleavage in apoptosis - Caspase 3-resistant PARP mutant increases rates of apoptosis in transfected cells [J].
Boulares, AH ;
Yakovlev, AG ;
Ivanova, V ;
Stoica, BA ;
Wang, GP ;
Iyer, S ;
Smulson, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) :22932-22940
[7]
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
[8]
Comparison of acute responses of mice livers to short-term exposure to nano-sized or micro-sized silver particles [J].
Cha, Kyungeun ;
Hong, Hye-Won ;
Choi, Yeon-Gil ;
Lee, Min Joo ;
Park, Jong Hoon ;
Chae, Hee-Kwon ;
Ryu, Gyuha ;
Myung, Heejoon .
BIOTECHNOLOGY LETTERS, 2008, 30 (11) :1893-1899
[9]
Formation of nucleoplasmic protein aggregates impairs nuclear function in response to SiO2 nanoparticles [J].
Chen, M ;
von Mikecz, A .
EXPERIMENTAL CELL RESEARCH, 2005, 305 (01) :51-62
[10]
PUMA couples the nuclear and cytoplasmic proapoptotic function of p53 [J].
Chipuk, JE ;
Bouchier-Hayes, L ;
Kuwana, T ;
Newmeyer, DD ;
Green, DR .
SCIENCE, 2005, 309 (5741) :1732-1735