- Nano Express
- Open Access
Effect of amorphous silica nanoparticles on in vitro RANKL-induced osteoclast differentiation in murine macrophages
- Hiromi Nabeshi1, 2,
- Tomoaki Yoshikawa1, 2Email author,
- Takanori Akase1, 2,
- Tokuyuki Yoshida1, 2,
- Saeko Tochigi1, 2,
- Toshiro Hirai1, 2,
- Miyuki Uji1, 2,
- Ko-ichi Ichihashi1, 2,
- Takuya Yamashita1, 2,
- Kazuma Higashisaka1, 2,
- Yuki Morishita1, 2,
- Kazuya Nagano2,
- Yasuhiro Abe2,
- Haruhiko Kamada2, 3,
- Shin-ichi Tsunoda2, 3, 4,
- Norio Itoh1, 2,
- Yasuo Yoshioka2, 3 and
- Yasuo Tsutsumi1, 2, 3Email author
© Nabeshi et al; licensee Springer. 2011
- Received: 18 April 2011
- Accepted: 22 July 2011
- Published: 22 July 2011
Amorphous silica nanoparticles (nSP) have been used as a polishing agent and/or as a remineralization promoter for teeth in the oral care field. The present study investigates the effects of nSP on osteoclast differentiation and the relationship between particle size and these effects. Our results revealed that nSP exerted higher cytotoxicity in macrophage cells compared with submicron-sized silica particles. However, tartrate-resistant acid phosphatase (TRAP) activity and the number of osteoclast cells (TRAP-positive multinucleated cells) were not changed by nSP treatment in the presence of receptor activator of nuclear factor κB ligand (RANKL) at doses that did not induce cytotoxicity by silica particles. These results indicated that nSP did not cause differentiation of osteoclasts. Collectively, the results suggested that nanosilica exerts no effect on RANKL-induced osteoclast differentiation of RAW264.7 cells, although a detailed mechanistic examination of the nSP70-mediated cytotoxic effect is needed.
- silicon dioxide
- osteoclast differentiation
Recently, amorphous silica nanoparticles (nSP) with a controlled particle size below 100 nm have been a focus of investigations in various fields of industry. nSP have been used in a number of different industrial applications such as medicine, cosmetics and foods. In addition, the usability of nSP has been demonstrated in the oral care field, e.g. as a polishing agent and/or as a remineralization promoter for teeth [1, 2]. It has been reported that about 20% of toothpastes contain nSP. Because nSP have already become commonly used materials, it is difficult to imagine our daily life without them. Furthermore, given the recent use of smaller-sized and/or well-dispersed silica particles in various fields, it is expected that the use of these particles will increase in the future. On the other hand, there have been many reports that nSP exert biological effects that are not induced by conventional silica particles [3, 4], although the reasons for the effects of particle size on biological responses were unclear. There are growing concerns about the safety of nSP . However, current risk analyses do not yet focus sufficiently on the particle sizes. Accordingly, there is a compelling need to clarify the biological and cellular responses induced by different particle sizes. To ensure the safe production and use of nSP, it is very important to collect safety information on them via properly designed studies, taking into consideration exposure levels and cellular responses.
Our group carried out a previous study of the safety of nSP and revealed that surface unmodified nSP could pass though the skin barrier, migrate into the bloodstream and circulate throughout the entire body . This suggests that nSP may be absorbed through the oral mucosa easily when nSP, including oral care products, are used. Furthermore, it is possible that nSP circulating in the blood can reach the alveolar bone, which is presented in the submucosal layer, as well as various cells such as macrophages and osteoblasts. In particular, macrophages are known as multifunctional cells, as they can function not only as immunocompetent cells, but also as pre-osteoclasts . Osteoclasts that resorb bone play an important role in bone remodelling. Osteoclastogenesis involves complex pathways with intricate relationships between multiple signalling molecules. In particular, receptor activator of nuclear factor κB ligand (RANKL) is known to be a key molecule that initiates osteoclast formation . In addition, reactive oxygen species (ROS) and pro-inflammatory cytokines such as interleukin (IL)-1, IL-6, IL-8 and tumour necrosis factor alpha are potent stimulators of osteoclast formation and activity [9–11]. Our studies revealed that nSP induced high ROS and pro-inflammatory cytokine production, and these cellular responses may induce excess osteoclast differentiation. Acceleration of osteoclast differentiation, that is excess bone resorption, accelerates the onset of osteoporosis, arthritis and periodontal disease [12–14]. Therefore, we consider that it is necessary to estimate nSP-induced effects on osteoclast differentiation. Furthermore, because we indicated previously that nSP induced different cellular responses from submicron-sized silica particles, such as those described above, it was of interest to analyse the effects of particle size on osteoclast differentiation. Here, we investigate nSP-induced effects on osteoclast differentiation and the relationship between particle size and these effects.
Suspensions of amorphous silica particles (Micromod Partikeltechnologie GmbH, Warnemuende, Germany) (25 and 50 mg/ml) were used in this study; particle size diameters were 70, 300 and 1,000 nm (designated as nSP70, nSP300 and mSP1000, respectively). Silica particle suspensions were stored at room temperature. The suspensions were sonicated for 5 min and then vortexed for 1 min immediately prior to use.
The mouse macrophage cell line RAW264.7 was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). RAW264.7 cells were cultured in Dulbecco's Modified Eagle Medium supplemented with 10% heat-inactivated fetal calf serum (FCS), 1% antibiotic-antimycotic mix stock solution (Invitrogen Corporation, Carlsbad, CA, USA). All cultures were incubated at 37°C in a humidified atmosphere with 5% CO2.
The cytotoxicity of silica particle-treated RAW264.7 cells and untreated cells was assessed using a WST-8 assay. Cells, 1.5 × 103, were cultured with varying concentrations of silica particles diluted with medium for 5 days at 37°C and 10 μl of Cell Count Reagent SF (Nacalai Tesque, Inc., Kyoto, Japan) was then added into each well. After 1 h, absorbance was measured at 450 nm (reference, 650 nm) using a microplate reader (Mithras LB940; BERTHOLD TECHNOLOGIES GmbH & Co. KG, Bald Wildbad, Germany).
TRAP staining and activity assay
Osteoclast differentiation of silica particle-treated RAW264.7 cells was assessed by tartrate-resistant acid phosphatase (TRAP) staining and activity. RAW264.7 cells were suspended in phenol red-free α-MEM containing 10% heat-inactivated FCS, 1% antibiotic-antimycotic mix stock solution. Cells numbering 2 × 104 per well were cultured in 48-well plates with 10 μg/ml of silica particles and RANKL (30 ng/ml) diluted with phenol red-free medium for 5 days. TRAP staining was carried out using a TRAP/alkaline phosphatase (ALP) stain kit (Wako Pure Chemicals Industries Ltd., Osaka, Japan) according to the protocol provided in the kit. Images of TRAP-positive multinucleated cells (number of nuclei > 3) were captured with a microscope. To measure TRAP activity, cells were fixed with 10% formalin for 10 min and 95% ethanol for 1 min, and then 100 μl of citrate buffer (50 mM, pH 4.6) containing 10 mM sodium tartrate and 5 mM p-nitrophenylphosphate (Sigma-Aldrich Corporation, St. Louis, MO, USA) was added to the wells containing fixed cells in the 48-well plates. After incubation for 1 h, enzyme reaction mixtures in the wells were transferred to new plates containing an equal volume of 0.1 N NaOH. Absorbance was measured at 410 nm using a microplate reader (Mithras LB940; BERTHOLD TECHNOLOGIES GmbH & Co. KG, Bald Wildbad, Germany). Each experiment was performed in triplicate.
All data are reported as the mean ± SD. The significance of variation among different groups was determined by one-way ANOVA. Differences between the experimental and control groups were determined using the Bonferroni test. P < 0.05 was considered significant.
This study evaluated the effects of amorphous silica particles on osteoclast differentiation of macrophage cells, using silica particles of 70 (nSP70), 300 (nSP300) and 1,000 nm (mSP1000) in diameter. We previously confirmed that these silica particles were spherical, and the primary particle sizes were approximately uniform . In addition, none of the silica particles used in this study were modified with any functional groups, and their surfaces were nonporous. The mean particle size in PBS suggested that the silica particles used in this study remained as stable well-dispersed particles in solution, i.e. they did not aggregate .
In the dentistry field, it is well-known that wear particles from materials used in implants can induce bone destruction, and this can become a significant therapeutic problem in the treatments requiring implants and/or artificial bone. Some reports have suggested that micro-sized particles (about 4-9 μm in diameter) increased the expression of RANKL and/or osteoclast differentiation-related genes in bone marrow cells [16, 17]. These reports suggested that micro-sized particles above 4 μm accelerated the osteoclast differentiation. On the other hand, in the case of nano- and subnano-sized particles, it has been reported that particles did not affect osteoclast differentiation or the expression of inflammatory cytokines and osteoclast differentiation-regulated genes . Our earlier results and the present report suggest that acceleration effects of particles on osteoclast differentiation slowed as the particles got smaller, until they reached nanosize. In other words, the particle size is an important characteristic in the ability of nanoparticles to induce osteoclast differentiation. The mechanism by which cells take up particles differs according to particle sizes . The larger particles (from several micrometers to several dozen micrometers) and the smaller particles (from several dozen to several hundred nanometers) are believed to be taken up by macrophage cells via phagocytosis and macropinocytosis, respectively . Therefore, these differences of particle uptake pathway may be one of the factors producing the observed effect of particle size on osteoclast differentiation.
Collectively, the results presented here indicated that nanosilica has no effect on osteoclast differentiation. They also support the safety of nanosilicas that are used in the production of highly functional materials for oral care fields [1, 20]. We believe that applications of nanosilica will extend to these new fields in the near future following further careful safety study.
This study was supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT), and from the Japan Society for the Promotion of Science (JSPS); and by a the Knowledge Cluster Initiative (MEXT); by Health Labour Sciences Research Grants from the Ministry of Health, Labour and Welfare of Japan (MHLW); by a Global Environment Research Fund from Minister of the Environment; by Food Safety Commission (Cabinet Office); by The Cosmetology Research Foundation; by The Smoking Research Foundation; and by The Takeda Science Foundation.
- Gaikwad RM, Sokolov I: Silica nanoparticles to polish tooth surfaces for caries prevention. J Dent Res 2008, 87: 980–983. 10.1177/154405910808701007View ArticleGoogle Scholar
- Liao WQ, Zang YL, Shao JZ: Sporotrichosis presenting as pyoderma gangrenosum. Mycopathologia 1991, 116: 165–168. 10.1007/BF00436831View ArticleGoogle Scholar
- Napierska D, Thomassen LC, Lison D, Martens JA, Hoet PH: The nanosilica hazard: another variable entity. Part Fibre Toxicol 2010, 7: 39. 10.1186/1743-8977-7-39View ArticleGoogle Scholar
- Yamashita K, Yoshioka Y, Higashisaka K, Mimura K, Morishita Y, Nozaki M, Yoshida T, Ogura T, Nabeshi H, Nagano K, Abe Y, Kamada H, Monobe Y, Imazawa T, Aoshima H, Shishido K, Kawai Y, Mayumi T, Tsunoda SI, Itoh N, Yoshikawa T, Yanagihara I, Saito S, Tsutsumi Y: Nat Nanotechnol. 2011, in press.Google Scholar
- Maynard AD, Aitken RJ, Butz T, Colvin V, Donaldson K, Oberdörster G, Philbert MA, Ryan J, Seaton A, Stone V, Tinkle SS, Tran L, Walker NJ, Warheit DB: Safe handling of nanotechnology. Nature 2006, 444: 267–269. 10.1038/444267aView ArticleGoogle Scholar
- Nabeshi H, Yoshikawa T, Matsuyama K, Nakazato Y, Matsuo K, Arimori A, Isobe M, Tochigi S, Kondoh S, Hirai T, Akase T, Yamashita T, Yamashita K, Yoshida T, Nagano K, Abe Y, Yoshioka Y, Kamada H, Imazawa T, Itoh N, Nakagawa S, Mayumi T, Tsunoda S, Tsutsumi Y: Systemic distribution, nuclear entry and cytotoxicity of amorphous nanosilica following topical application. Biomaterials 2011, 32: 2713–2724. 10.1016/j.biomaterials.2010.12.042View ArticleGoogle Scholar
- Ash P, Loutit JF, Townsend KM: Osteoclasts derived from haematopoietic stem cells. Nature 1980, 283: 669–670. 10.1038/283669a0View ArticleGoogle Scholar
- Suda T, Takahashi N, Udagawa N, Jimi E, Gillespie MT, Martin TJ: Modulation of osteoclast differentiation and function by new members of the tumor necrosis factor receptor and ligand families. Endocr Rev 1999, 20: 345–357. 10.1210/er.20.3.345View ArticleGoogle Scholar
- Dougall WC, Glaccum M, Charrier K, Rohrbach K, Brasel K, De Smedt T, Daro E, Smith J, Tometsko ME, Maliszewski CR, Armstrong A, Shen V, Bain S, Cosman D, Anderson D, Morrissey PJ, Peschon JJ, Schuh J: RANK is essential for osteoclast and lymph node development. Genes Dev 1999, 13: 2412–2424. 10.1101/gad.13.18.2412View ArticleGoogle Scholar
- Wiktor-Jedrzejczak W, Bartocci A, Ferrante AW, Ahmed-Ansari A, Sell KW, Pollard JW, Stanley ER: Total absence of colony-stimulating factor 1 in the macrophage-deficient osteopetrotic (op/op) mouse. Proc Natl Acad Sci USA 1990, 87: 4828–4832. 10.1073/pnas.87.12.4828View ArticleGoogle Scholar
- Yoshida H, Hayashi S, Kunisada T, Ogawa M, Nishikawa S, Okamura H, Sudo T, Shultz LD: The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene. Nature 1990, 345: 442–444. 10.1038/345442a0View ArticleGoogle Scholar
- Takayanagi H: Osteoimmunology: shared mechanisms and crosstalk between the immune and bone systems. Nat Rev Immunol 2007, 7: 292–304. 10.1038/nri2062View ArticleGoogle Scholar
- Teitelbaum SL, Ross FP: Genetic regulation of osteoclast development and function. Nat Rev Genet 2003, 4: 638–649. 10.1038/nrg1122View ArticleGoogle Scholar
- Theill LE, Boyle WJ, Penninger JM: RANK-L and RANK: T cells, bone loss, and mammalian evolution. Annu Rev Immunol 2002, 20: 795–823. 10.1146/annurev.immunol.20.100301.064753View ArticleGoogle Scholar
- Nabeshi H, Yoshikawa T, Matsuyama K, Nakazato Y, Arimori A, Isobe M, Tochigi S, Kondoh S, Hirai T, Akase T, Yamashita T, Yamashita K, Yoshida T, Nagano K, Abe Y, Yoshioka Y, Kamada H, Imazawa T, Itoh N, Tsunoda S, Tsutsumi Y: Size-dependent cytotoxic effects of amorphous silica nanoparticles on Langerhans cells. Pharmazie 2010, 65: 199–201.Google Scholar
- Clohisy JC, Frazier E, Hirayama T, Abu-Amer Y: RANKL is an essential cytokine mediator of polymethylmethacrylate particle-induced osteoclastogenesis. J Orthop Res 2003, 21: 202–212. 10.1016/S0736-0266(02)00133-XView ArticleGoogle Scholar
- Pioletti DP, Kottelat A: The influence of wear particles in the expression of osteoclastogenesis factors by osteoblasts. Biomaterials 2004, 25: 5803–5808. 10.1016/j.biomaterials.2004.01.053View ArticleGoogle Scholar
- Tautzenberger A, Kreja L, Zeller A, Lorenz S, Schrezenmeier H, Mailänder V, Landfester K, Ignatius A: Direct and indirect effects of functionalised fluorescence-labelled nanoparticles on human osteoclast formation and activity. Biomaterials 2010, 32: 1706–1714.View ArticleGoogle Scholar
- Hillaireau H, Couvreur P: Nanocarriers' entry into the cell: relevance to drug delivery. Cell Mol Life Sci 2009, 66: 2873–2896. 10.1007/s00018-009-0053-zView ArticleGoogle Scholar
- Muller WE, Boreiko A, Wang X, Krasko A, Geurtsen W, Custodio MR, Winkler T, Lukic-Bilela L, Link T, Schroder HC: Morphogenetic activity of silica and bio-silica on the expression of genes controlling biomineralization using SAOS-2 cells. Calcif Tissue Int 2007, 81: 382–393. 10.1007/s00223-007-9075-4View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.