Inflammasome formation and IL-1β release by human blood monocytes in response to silver nanoparticles

被引:192
作者
Yang, Eun-Jeong [1 ]
Kim, Seungjae [1 ]
Kim, Jong Soo [1 ]
Choi, In-Hong [1 ]
机构
[1] Yonsei Univ, Coll Med, Inst Immunol & Immunol Dis, Brain Korea Project Med Sci 21,Dept Microbiol, Seoul 120752, South Korea
基金
新加坡国家研究基金会;
关键词
Silver nanoparticles; IL-1; beta; NLRP3; inflammasome; Caspase-1; Mitochondrial superoxide; NLRP3; INFLAMMASOME; HUMAN MACROPHAGES; DENDRITIC CELLS; MITOCHONDRIA; ACTIVATION; INDUCTION; APOPTOSIS; INNATE; IMMUNITY; SILICA;
D O I
10.1016/j.biomaterials.2012.06.016
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study, the immunological effect of silver nanoparticles on innate immunity was investigated using primary human monocytes. After exposure to silver nanoparticles, production of IL-1 beta, a critical cytokine involved in induction of innate immunity, significantly increased as particle size decreased. These results suggest that silver nanoparticles may evoke an immunologically active state. The size effect of silver nanoparticles on IL-1 beta production was also further investigated. 5 nm and 28 nm silver nanoparticles induced inflammasome formation and subsequent caspase-1 activation. Using inhibitors, we found exposure to silver nanoparticles caused leakage of cathepsins from lysosomes and efflux of intracellular K+. These two events induced superoxide within mitochondrial membranes, leading to inflammasome formation. 5 nm silver nanoparticles produced more hydrogen peroxide and were more cytotoxic than 28 nm silver nanoparticles, suggesting the balance between superoxide and hydrogen peroxide governs cell fate, death or activation. Moreover, these findings also suggest that the immunological significance of silver nanoparticles should be considered with respect to their capacity to synergistically activate immune responses. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6858 / 6867
页数:10
相关论文
共 32 条
[1]   Apoptosis induction by silica nanoparticles mediated through reactive oxygen species in human liver cell line HepG2 [J].
Ahmad, Javed ;
Ahamed, Maqusood ;
Akhtar, Mohd Javed ;
Alrokayan, Salman A. ;
Siddiqui, Maqsood A. ;
Musarrat, Javed ;
Al-Khedhairy, Abdulaziz A. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2012, 259 (02) :160-168
[2]   Mitochondria in innate immunity [J].
Arnoult, Damien ;
Soares, Fraser ;
Tattoli, Ivan ;
Girardin, Stephen E. .
EMBO REPORTS, 2011, 12 (09) :901-910
[3]   Mitochondria, oxidants, and aging [J].
Balaban, RS ;
Nemoto, S ;
Finkel, T .
CELL, 2005, 120 (04) :483-495
[4]   The role of the NLRP3 Inflammasome in the pathogenesis of airway disease [J].
Birrell, Mark A. ;
Eltom, Suffwan .
PHARMACOLOGY & THERAPEUTICS, 2011, 130 (03) :364-370
[5]   Mitochondrial reactive oxygen species promote production of proinflammatory cytokines and are elevated in TNFR1-associated periodic syndrome (TRAPS) [J].
Bulua, Ariel C. ;
Simon, Anna ;
Maddipati, Ravikanth ;
Pelletier, Martin ;
Park, Heiyoung ;
Kim, Kye-Young ;
Sack, Michael N. ;
Kastner, Daniel L. ;
Siegel, Richard M. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (03) :519-533
[6]   Regulation of adaptive immunity by the NLRP3 inflammasome [J].
Chen, Mingkuan ;
Wang, Hongbin ;
Chen, Wei ;
Meng, Guangxun .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2011, 11 (05) :549-554
[7]  
Jang Jiyoung, 2010, Immune Netw, V10, P85, DOI 10.4110/in.2010.10.3.85
[8]   Molecular Mechanism of NLRP3 Inflammasome Activation [J].
Jin, Chengcheng ;
Flavell, Richard A. .
JOURNAL OF CLINICAL IMMUNOLOGY, 2010, 30 (05) :628-631
[9]  
양은정, 2012, Journal of Bacteriology and Virology, V42, P177, DOI 10.4167/jbv.2012.42.2.177
[10]  
Karin N, 2004, CURR OPIN MOL THER, V6, P27