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http://dx.doi.org/10.4110/in.2012.12.6.296

The Effects of Silica Nanoparticles in Macrophage Cells  

Kim, Seungjae (Department of Microbiology, The Institute for Immunology and Immunological Diseases, College of Medicine, Yonsei University)
Jang, Jiyoung (Department of Microbiology, The Institute for Immunology and Immunological Diseases, College of Medicine, Yonsei University)
Kim, Hyojin (Department of Microbiology, The Institute for Immunology and Immunological Diseases, College of Medicine, Yonsei University)
Choi, Hoon (Department of Chemical and Biomolecular Engineering, Yonsei University)
Lee, Kangtaek (Department of Chemical and Biomolecular Engineering, Yonsei University)
Choi, In-Hong (Department of Microbiology, The Institute for Immunology and Immunological Diseases, College of Medicine, Yonsei University)
Publication Information
IMMUNE NETWORK / v.12, no.6, 2012 , pp. 296-300 More about this Journal
Abstract
Silica nanoparticles, which are applicable in many industrial fields, have been reported to induce cellular changes such as cytotoxicity in various cells and fibrosis in lungs. Because the immune system is the primary targeting organ reacting to internalized exogenous nanoparticles, we tried to figure out the immunostimulatory effect of silica nanoparticles in macrophages using differently sized silica nanoparticles. Using U937 cells we assessed cytotoxicity by CCK-8 assay, ROS generation by CM-$H_2DCFDA$, intracellular $Ca^{{+}{+}}$ levels by staining with Fluo4-AM and IL-8 production by ELISA. At non-toxic concentration, the intracellular $Ca^{{+}{+}}$ level has increased immediately after exposure to 15 nm particles, not to larger particles. ROS generation was detected significantly in response to 15 nm particles. However, all three different sizes of silica nanoparticles induced IL-8 production. 15 nm silica nanoparticles are more stimulatory than larger particles in cytotoxicity, intracellular $Ca^{{+}{+}}$ increase and ROS generation. But IL-8 production was induced to same levels with 50 or 100 nm particles. Therefore, IL-8 production induced by silica nanoparticles may be dependent on other mechanisms rather than intracellular $Ca^{{+}{+}}$ increase and ROS generation.
Keywords
Silica nanoparticles; Macrophages; Intracellular $Ca^{{+}{+}}$ level; ROS; IL-8;
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1 Chen, Z., H. Meng, G. Xing, H. Yuan, F. Zhao, R. Liu, X. Chang, X. Gao, T. Wang, G. Jia, C. Ye, Z. Chai, and Y. Zhao. 2008. Age-related differences in pulmonary and cardiovascular responses to SiO2 nanoparticle inhalation: nanotoxicity has susceptible population. Environ. Sci. Technol. 42: 8985-8992.   DOI
2 Bhattacharya, K., P. C. Naha, I. Naydenova, S. Mintova, and H. J. Byrne. 2012. Reactive oxygen species mediated DNA damage in human lung alveolar epithelial (A549) cells from exposure to non-cytotoxic MFI-type zeolite nanoparticles. Toxicol. Lett. 215: 151-160.   DOI
3 Chu, Z., Y. Huang, L. Li, Q. Tao, and Q. Li. 2012. Physiological pathway of human cell damage induced by genotoxic crystalline silica nanoparticles. Biomaterials 33: 7540-7546.   DOI
4 Zhang, Z. and A. Chai. 2012. Core-shell magnetite-silica composite nanoparticles enhancing DNA damage induced by a photoactive platinum-diimine complex in red light. J. Inorg. Biochem. 117: 71-76.   DOI
5 Borak, B., P. Biernat, A. Prescha, A. Baszczuk, and J. Pluta. 2012. In vivo study on the biodistribution of silica particles in the bodies of rats. Adv. Clin. Exp. Med. 21: 13-18.
6 Feng, X., D. C. Sayle, Z. L. Wang, M. S. Paras, B. Santora, A. C. Sutorik, T. X. Sayle, Y. Yang, Y. Ding, X. Wang, and Y. S. Her. 2006. Converting ceria polyhedral nanoparticles into single-crystal nanospheres. Science 312: 1504-1508.   DOI
7 Anas, A., J. Jiya, M. J. Rameez, P. B. Anand, M. R. Anantharaman, and S. Nair. 2013. Sequential interactions of silver- silica nanocomposite (Ag-SiO(2) NC) with cell wall, metabolism and genetic stability of Pseudomonas aeruginosa, a multiple antibiotic-resistant bacterium. Lett. Appl. Microbiol. 56: 57-62.   DOI
8 Li, X., Y. Chen, M. Wang, Y. Ma, W. Xia, and H. Gu. 2013. A mesoporous silica nanoparticle - PEI - Fusogenic peptide system for siRNA delivery in cancer therapy. Biomaterials 34:1391-1401.   DOI
9 Scalia, S., E. Franceschinis, D. Bertelli, and V. Iannuccelli. 2012. Comparative Evaluation of the Effect of Permeation Enhancers, Lipid Nanoparticles and Colloidal Silica on in vivo Human Skin Penetration of Quercetin. Skin Pharmacol. Physiol. 26: 57-67.
10 Kim, S. and I. H. Choi. 2012. Phagocytosis and endocytosis of silver nanoparticles induce interleukin-8 production in human macrophages. Yonsei Med. J. 53: 654-657.   DOI
11 Yang, E. J., S. Kim, J. S. Kim, and I. H. Choi. 2012. Inflammasome formation and IL-$1{\beta}$ release by human blood monocytes in response to silver nanoparticles. Biomaterials 33: 6858-6867.   DOI
12 Lim, D. H., J. Jang, S. Kim, T. Kang, K. Lee, and I. H. Choi. 2012. The effects of sub-lethal concentrations of silver nanoparticles on inflammatory and stress genes in human macrophages using cDNA microarray analysis. Biomaterials 33: 4690-4699.   DOI
13 Park, J., D. H. Lim, H. J. Lim, T. Kwon, J. S. Choi, S. Jeong, I. H. Choi, and J. Cheon. 2011. Size dependent macrophage responses and toxicological effects of Ag nanoparticles. Chem. Commun. (Camb.) 47: 4382-4384.   DOI