- Open Access
Nickel oxide nanoparticles can recruit eosinophils in the lungs of rats by the direct release of intracellular eotaxin
© The Author(s). 2016
- Received: 11 December 2015
- Accepted: 2 June 2016
- Published: 9 June 2016
Instillation of highly soluble nanoparticles (NPs) into the lungs of rodents can cause acute eosinophilia without any previous sensitizations by the role of dissolved ions. However, whether gradually dissolving NPs can cause the same type of eosinophilia remains to be elucidated. We selected nickel oxide (NiO) as a gradually dissolving NP and evaluated the time course pulmonary inflammation pattern as well as its mechanisms.
NiO NPs were intratracheally instilled into female Wistar rats at various concentrations (50, 100, and 200 cm2/rat) and the lung inflammation was evaluated at various time-points (1, 2, 3, and 4 days). As positive controls, NiCl2 and the ovalbumin-induced allergic airway inflammation model was applied. NiCl2 was instilled at 171.1 μg Ni/rat, which is equivalent nickel concentration of 200 cm2/rat of NiO NPs. Cytological analysis and biochemical analysis including lactate dehydrogenase (LDH), total protein, and pro-inflammatory cytokines were measured in bronchoalveolar lavage fluid (BALF). The levels of total immunoglobulin E (IgE) and anaphylatoxins (C3a and C5a) were measured in BALF and serum. The levels of eotaxin were measured in the alveolar macrophages and normal lung tissue before and after addition of cell lysis buffer to evaluate whether the direct lysis of cells can release intracellular eotaxin.
NiO NPs produced acute neutrophilic inflammation throughout the study. However, eosinophils were recruited at 3 and 4 days post-instillation of NiO NPs and the magnitude and pattern of inflammation was similar with NiCl2 at 24 h post-instillation. The eosinophil recruitment by NiO NPs was not related with either the levels of total IgE or anaphylatoxins. The lysis of alveolar macrophages and normal lung tissue showed high levels of intracellular eotaxin and the levels of LDH showed positive correlation with the levels of eotaxin.
Instillation of NiO NPs produced neutrophilia at 1 and 2 days after instillation, while the mixed type of neutrophilic and eosinophilic inflammation was produced at 3 and 4 days post-instillation, which was consistent with NiCl2. The mechanism of the eosinophilia involves the direct release of intracellular eotaxin due to the rupture of cells by the accumulated solubilized nickel ions in the phagolysosome.
- Nickel oxide nanoparticles
Several mechanisms have been known to cause eosinophilic inflammation including the immunoglobulin E (IgE)-mediated allergic response as well as anaphylatoxins by the complement activation cascade. IgE-mediated eosinophilia, commonly known as an allergic reaction, can be produced by an immunological response synchronized by several sensitization processes against a certain allergen  or parasite infection . The activation of complement releases anaphylatoxins (e.g., C3a and C5a) and produces eosinophilia by histamine release from mast cells. This type of inflammation is generally called as pseudoallergy or drug hypersensitivity . In our recent studies, however, some metal oxide nanoparticles (NPs) were found to cause pulmonary eosinophilia within 24 h without any previous sensitization . Although previous studies showed that instillation of TiO2 promotes allergic sensitization and lung inflammation in the ovalbumin (OVA)-sensitization mouse model , and that liposome-based NPs produced complement-mediated hypersensitivity , the mechanism of eosinophilia by metal oxide NPs (e.g., CoO, CuO, and ZnO) within 24 h without any previous sensitization is new finding that deserves further investigation [7–9].
Acute eosinophil infiltration caused by metal oxide NPs has been reported with highly soluble NPs; the dissolved metal ions in the acidic phagolysosomes of phagocytes play a critical role in recruiting eosinophils. When highly soluble NPs are inhaled, NPs remain insoluble in the alveoli, but are dissolved soon after phagocytosis, releasing their compositional ions . Indeed, several highly soluble NPs produced acute eosinophilic airway inflammation in rodents via their soluble metal ions [7, 9]. The molecular mechanism of eosinophilia by NPs involves the direct induction of the eotaxin protein; however, the signaling pathway for eotaxin gene expression is still poorly understood . Furthermore, other possible mechanisms for eosinophil infiltration by metal oxide NPs (e.g., IgE-mediated or anaphylatoxins by complement activation) are still in question.
Solubility is one of the key issues in triggering the eosinophilic inflammation of metal oxide NPs. All NPs known to produce eosinophilia in the lung are highly soluble NPs (e.g., CoO, CuO, and ZnO), but whether gradually dissolving NPs can produce eosinophilia is not known. Therefore, follow-on our previous study, we hypothesized, in this study, that gradually dissolving NPs can produce pulmonary eosinophilia by accumulating solubilized ions in phagocytes with a delayed time frame as compared with highly soluble NPs. We selected NiO NPs as a representative gradually dissolving NP based on our previous study , and investigated the time course of inflammation and its underlying mechanism using a rat intratracheal instillation model.
Physicochemical characterization of NiO NPs
Physicochemical characterization of NiO NPs
Mean ± SEM
Primary size (nm)
5.3 ± 0.4
Surface area (m2/g)
Hydrodynamic size (nm) in
209 ± 3.7
970 ± 52
PBS with 3 % rat serum
224 ± 11
0.30 ± 0.02
0.65 ± 0.05
PBS with 3 % rat serum
0.45 ± 0.06
Zeta potential (mV) in
48.9 ± 0.6
−21 ± 0.6
PBS with 3 % rat serum
−30 ± 2.3
Solubility (%) in
PBS (pH 7.4)
PBS with 3 % rat serum
Artificial lysosomal fluid (pH 5.5)
Pulmonary inflammation pattern evaluated by differential cell counts of BALF
Levels of Ni in BALF
The levels of Ni in BALF of 200 cm2/rat of NiO NPs showed significant increases at all time-points (Figure S3, see Additional file 1). The levels of Ni were peaked at 1 or 2 days after instillation and showed slightly decreasing trend thereafter.
Levels of lactate dehydrogenase (LDH) and total protein in BALF
Expression of pro-inflammatory cytokines in BALF
Levels of total IgE and anaphylatoxins (C3a and C5a) in serum and BALF
Levels of intracellular eotaxin in alveolar macrophages and normal lung tissue
Positive correlation between levels of LDH and eotaxin
To our knowledge, NiO NPs are gradually dissolving NPs that release a significant amount of nickel ions into the lysosomes of phagocytes and require more than 1 month for complete dissolution . Previous studies on the pulmonary exposure of NiO NPs reported that NiO NPs in the lung produced acute neutrophilic inflammation via surface reactivity such as the generation of reactive oxygen species (ROS) [13, 14], while chronic active pulmonary inflammation with immunological T helper type 1 (Th1-type) hypersensitivity was produced by the chronic coexistence of NPs and haptenic soluble nickel ions . In this study, we found that the instillation of NiO NPs produced massive eosinophilic inflammation during the period of acute neutrophilic inflammation. The various inflammatory patterns by NiO NPs including neutrophilia, eosinophilia, and chronic active/Th-1 hypersensitivity is very unique and has not been reported yet by any materials.
The eosinophilia of NiO NPs with a delayed-time frame (3 and 4 days after instillation) and immediate (1 day after instillation) eosinophilia by NiCl2 might provide an important clue for the mechanism of the immediate eotaxin release by highly soluble NPs (e.g., CoO, CuO, and ZnO) [7, 8]. Because eotaxin is stored in the cytoplasm of various normal cells such as the epithelial cell, fibroblast, and macrophage [15, 16], the lysis of these cells can release a significant amount of eotaxin protein. The delayed time frame of eosinophilia by NiO NPs found in this study might be due to the delayed rupture of cells by the accumulation of a significant amount of nickel ions from the NiO NPs in the phagolysosomes, because NiO NPs showed about 9.5 % dissolution/day in the acidic artificial lysosomal fluid. The increased levels of nickel in BALF measured in this study also confirm the dissolved nickel ions from NiO NPs. The role of nickel ions on recruiting eosinophils is supported not only by the increased levels of eotaxin at 1 day after instillation of NiCl2 which observed in this study, but also by the increased eotaxin levels of the highly soluble NPs (CoO, CuO, and ZnO) and their composition ions (CoCl2 and ZnCl2) at 1 day after instillation in our previous studies [8, 11]. No reports about the direct induction of eosinophilia by poorly soluble NPs without any previous sensitizations and the correlation plot of the levels of LDH, a marker for cell lysis, against the levels of eotaxin that was shown in this study also confirm this hypothesis. Therefore, this study can suggest one of main mechanisms of pulmonary eosinophilia by metal oxide NPs is the release of intracellular eotaxin from ruptured cells, following the accumulation of highly toxic soluble ions.
Eotaxin-1 (CCL11), which measured in this study is a potent chemoattractant for eosinophils and has been suggested as a therapeutic target as well as biomarker in various allergic diseases including asthma . Eotaxin is an eosinophil-selective chemokine and not responsible to neutrophils and monocytes because those cells are not expressing CCL11-specific ligands including CCR2, CCR3, and CCR5 . Eotaxin also regulates the baseline level of eosinophils in healthy status by constitutively expressing mRNA and/or protein in normal cells such as fibroblast, epithelial cells, endothelial cells, T cells, and macrophages [19–21]. Among various cell types, eosinophils possess much higher amount of eotaxin in matrix of crystalloid granules and release eotaxin by the activation of eosinophils . Therefore, the eosinophilia by NiO NPs found in this study might be firstly triggered by the directly released intracellular eotaxin by the rupture of phagocytic cells and then recruited eosinophils accelerate eosinophilia. However, further studies are needed to support this hypothetical mechanism of action.
While the direct induction of eotaxin was shown in this study, the involvement of IgE or complement activation by metal oxide NPs in the pulmonary eosinophilia was unknown. Previous studies showed that various metal oxide NPs (e.g., Fe2O3, TiO2, and ZnO) and carbon nanotubes have an adjuvant effect, promoting allergic airway inflammation in the OVA-sensitization mouse model [5, 22–24]. Because IgE-mediated airway inflammation essentially requires an allergenic epitope and several sensitization processes, the direct induction of IgE-response by metal oxide NPs in an acute phase without previous sensitizations is highly unlikely. The lack of significant increases in IgE and IL-4 levels in this study also confirms that the eosinophilia by NiO NPs was not produced by the Th2 response. However, the low levels of eotaxin in the OVA model found in this study might be due to the pattern of eotaxin expression is transient . The release of anaphylatoxins such as C3a and C5a via the complement cascade can also produce acute eosinophilia; previous studies showed that some micelles, liposomes, and NPs produce an acute allergic response [3, 26, 27]. However, those studies were performed not in inhalation models, but in intravenous injection models or in vitro systems using serum. No significant changes in C3a and C5a levels found in this study might imply that NiO NPs does not stimulate anaphylatoxins by complement activation in this experimental setting. However, a slightly increased levels of serum C5a at 1 day after instillation and the low group size cannot exclude that some effects on C5a.
The mechanism of eosinophilia by NiO NPs at day 3 and 4 after instillation might provide important information for the asthmatic lung disease induced by environmental particles such as diesel exhaust particles and particulate matter 2.5 (PM2.5). Indeed, several studies showed that increased human exposure to diesel exhaust particles and PM is related to increased asthma incidence [28, 29]. However, the exact mechanism for the development of the asthmatic lung by air pollution is still unknown, partly because these particles are complex and composed of multiple particle types and organic compounds. Epidemiological data suggests that asthma develops not only after sensitization with allergens including food allergens , but also by a non-allergic mechanism such as polycyclic aromatic hydrocarbons . Based on interesting literature on the zinc level in the PM with a positive trend with asthma morbidity , the direct induction of eotaxin protein by NiO NPs without involvement of IgE or complement activation can suggest one possible mechanism for this non-allergic asthmatic lung injury by PM and further studies are warranted.
Intratracheal instillation of NiO NPs in rats demonstrated a unique mixed type of neutrophilic and eosinophilic inflammation at 3 and 4 days after instillation, which was consistent with the inflammation by NiCl2 at 1 day after instillation. The mechanism of eosinophilia by NiO NPs is due to the involvement of the direct rupture of cells, releasing a significant level of intracellular eotaxin. In addition, the time frame for eosinophilia was variable depending on the solubility of NPs and the intrinsic toxicity of compositional metals. However, more studies are warranted to support this hypothetical mechanism of eosinophilia by metal oxide NPs.
Nanoparticles and characterization
NiO NPs were purchased from Nanostructured & Amorphous Materials, Inc. (Houston, TX, USA). Physicochemical characterization including surface area, primary size, hydrodynamic size, polydispersity, zeta potential, solubility, and levels of endotoxin contamination were determined. Briefly, the surface area was measuring using the BET (Brunauer, Emmett, and Teller) method in ParticleCIC Ltd. (Leeds, UK) with a Micromeritics TriStar 3000 analyzer (Micromeritics Ltd., Bedfordshire, UK). The shape and primary size of the NiO NPs was measured using TEM (JEM-1200EX II, JEOL, Tokyo, Japan) and FE-SEM (Hitachi, Tokyo, Japan) and the average size was calculated by measuring at least 200 separate particles using a built-in program (JEOL). The hydrodynamic size and zeta potential of NiO NPs in DW or in PBS with/without dispersion medium (3 % heat-activated rat serum) was measured by Zetasizer Nano-ZS (Malvern, Malvern Hill, UK) according to the manufacturer’s instruction. To measure the solubility of the NiO NPs, NPs were suspended in various conditions including PBS (pH 7.4), PBS with 3 % rat serum, and artificial lysosomal fluid (pH 5.5)  at 1 mg/mL and incubated for 24 h at room temperature with continuous stirring. The NP-free supernatants were collected by three rounds of centrifugation at 15000 g for 30 min and the absence of NPs were confirmed by dynamic light scattering using Zetasizer Nano-ZS (Malvern). The concentration of dissolved metal ions was measured by the Center for Collaborative Instruments at Dong-A University using inductively coupled mass spectrometry (ICP-MS; Agilent Technologies, Seoul, Korea). Solubility was calculated and expressed as a percentage of the detected mass of nickel over the initial mass of nickel in NiO NPs. The concentration of endotoxin of NiO NPs at 400 cm2/mL in sterile PBS, the equivalent dose for animal experimentation, was evaluated by an endpoint chromogenic Limulus Amoebocyte Lysate (LAL) assay kit (Cambrex, Walkersville, MD, USA) with a detection limit of 0.1 EU/mL.
Dispersion of NPs for animal experiment
Previous studies showed that NPs are tend to agglomerate when dispersed in medium and agglomerations are accelerated in high salt conditions such as PBS and saline . Therefore, we used serum protein as a dispersion medium to provide protein corona formation, which can improve dispersion of NPs in physiological condition as previously described . Briefly, the stock solution of NiO NPs was prepared by dispersion at 4000 cm2/mL (4360 μg/mL) in DW. The solution was sonicated for 10 min using a bath sonicator (Saehan-Sonic, Seoul, Korea) and heat-inactivated rat serum collected from healthy 6-week old female Wistar rats (Samtako, Gyeonggi-do, Korea) was added at 3 % of end concentration and sonicated for 5 min. Finally, Ca2+- and Mg2+-free PBS (Life Technologies, Gaithersburg, MD, USA) was added to the NP suspension to achieve pre-determined final concentrations (100, 200, and 400 cm2/mL) for animal experimentation, followed by sonication for 5 min in a bath sonicator (Saehan-Sonic).
Intratracheal instillation of NiO NPs
Animal protocols were reviewed and approved by the Institutional Animal Care and Use Committee in Dong-A University. Six-week old female Wistar rats (Samtako) were acclimatized for 7 days before experimentation. Rats were housed in an individually ventilated cage system with controlled temperature and humidity (22 ± 1 °C and 50 ± 10 %) with a 12 h light/dark cycle. NiO NP suspensions were intratracheally instilled into the lungs of rats at surface area doses of 50, 100, and 200 cm2/rat (54.5, 109, and 218 μg/rat) according to the previously described method . Briefly, rats were anesthetized by isoflurane inhalation (Piramal Critical Care, Bethlehem, PA, USA) using a rodent anesthesia system (VetEquip, Pleasanton, CA, USA), and intubated with a 16-gauge blunt polycarbonate catheter. Then 500 μL of NP suspension or vehicle control (PBS with 3 % rat serum) was instilled once using a sterile syringe.
OVA-induced allergic airway inflammation model
As a positive control for IgE-mediated allergic inflammation, the OVA-induced allergic airway inflammation model was established according to the previously described method, with slight modification . Briefly, 6-week old female Wistar rats were sensitized on days 0, 7, and 14 with an intraperitoneal injection of 1 mg OVA (Grade V, Sigma-Aldrich, St Louis, MO, USA) and 100 mg aluminum hydroxide (Sigma-Aldrich) in 1 mL sterile saline. On day 21, rats were challenged with 1 mg OVA by intratracheal instillation and then sacrificed on day 22 to collect the BALF and serum.
Intratracheal instillation of nickel ion (NiCl2)
Because we hypothesized that NiO NPs can produce eosinophilia via the accumulation of nickel ions in the phagolysosomes of phagocytes, NiCl2 were instilled into lungs of rats to demonstrate the direct effect of nickel ions. Our previous studies also showed that instillation CoCl2 and ZnCl2 produced similar magnitude of eosinophilia as observed in CoO and ZnO at an equal metal concentrations [8, 11]. Although NiO NPs in the lung might not completely dissolved in the lung within 3 days after instillation, we selected the dose of NiCl2 at 378.0 μg/rat (171.1 μg Ni/rat), which is equivalent nickel concentration of 200 cm2/rat of NiO NPs to evaluate whether the dissolved nickel from NiO NPs directly induce pulmonary eosinophilia or not. NiCl2 (Sigma-Aldrich) dissolved in sterile Ca2+- and Mg2+-free PBS (Life Technologies) was intratracheally instilled into the lungs of rats and then sacrificed at 24 h post-instillation to collect the BALF and serum.
Preparation of BALF
At each time point, rats were anesthetized by isoflurane inhalation (Piramal Critical Care) and euthanized by removing blood from the inferior vena cava. The trachea was then cannulated by 14-gauge blunt stainless-steel needle and lavaged in-situ with 8 mL sterile cold Ca2+- and Mg2+-free PBS (Life Technologies) 4 times. The recovery volumes of the first lavage were about 7 mL and the subsequent lavages were about 8 mL. The first lavage was collected separately, and the cell-free supernatant was kept at −70 °C for further assays. Cell pellets from 4 lavages were pooled for total cell counts and cytological evaluation. The total number of cells was counted using a NucleoCounter (Chemometec, Allerod, Denmark); 4 × 104 cells were attached to glass slides by spinning at 27 g for 5 min using a cytospin (Hanil, Seoul, Korea). Slides were then dried, fixed with 100 % methanol, and stained with Diff-Quik (Thermo Fisher Scientific, Waltham, MA, USA). Differential cell counting was performed under a light microscope based on the morphology of cells. A minimum of 300 cells per slide was counted.
Measurement of nickel levels in BALF
The levels of nickel in BALF were measured to understand the uptake and dissolution of NiO NPs in the lung. The cell-free first lavage was centrifuged at 15000 g for 30 min to collect NP-free supernatant. Then, the concentration of dissolved nickel ions in the supernatant was measured using inductively coupled mass spectrometry (ICP-MS; Agilent Technologies).
Measurement of LDH, total protein, and pro-inflammatory cytokines in BALF
The levels of LDH, a maker for cytotoxicity, were measured in BALF using an LDH assay kit (Roche Diagnostics, Mannheim, Germany). Total protein, a maker for vascular permeability, was measured in BALF using a bicinchoninic acid (BCA) assay kit (Thermo Fisher Scientific). To evaluate the underlying mechanism of inflammation by NiO NPs, pro-inflammatory cytokines related to acute neutrophilic inflammation (IL-1β and CINC-3), eosinophilic inflammation (eotaxin and IL-4), and Th1 response (IFN-γ) were measured in BALF using a Duoset enzyme-linked immunosorbent assay (ELISA) kit (all from R&D systems, Minneapolis, MN, USA).
Measurement of total IgE, C3a, and C5a in BALF and serum
To evaluate the mechanism of allergic lung inflammation, the level of total IgE was measured in BALF and serum using an ELISA kit (Komabiotech, Seoul, Korea) according to the manufacturer’s instruction. The levels of C3a and C5a, marker for complement activation, were measured in BALF and serum using a C3a ELISA kit (MBS2503333, MyBioSource, San Diego, CA, USA) and C5a ELISA kit (MBS2506864, MyBioSource).
Measurement of intracellular eotaxin in alveolar macrophages and normal lung tissue
To evaluate whether the direct lysis of cells can release intracellular eotaxin, the levels of eotaxin were measured using alveolar macrophages and normal lung tissue before and after addition of cell lysis buffer. To collect the alveolar macrophages, 6-week old female Wistar rats (Samtako) were sacrificed and lungs were lavaged 4 times with 8 mL of PBS and cell pellets were collected by simple centrifugation and suspended with 1 mL of PBS. The number of total cells was counted using a NucleoCounter (Chemometec) and cytospin slides were prepared to confirm that more than 99 % of cells in BALF are alveolar macrophages. Then, cell lysis buffer (Atto, Tokyo, Japan) was added at a volume of 1 mL for 1 × 107 cells. To evaluate the dose–response relationship, the cells were lysed at different concentrations of cell lysis buffer by serial dilution with PBS. On the other hand, normal lung tissue was collected from 6-week old female Wistar rats (Samtako) and homogenized using tissue homogenizer. Then, cell lysis buffer (Atto) was added at a volume of 1 mL for 50 mg of lung tissue. Cell lysis buffer was serially diluted with PBS to evaluate the dose–response relationship. Alveolar macrophages and tissue homogenates were incubated with cell lysis buffer for 30 min and cell-free supernatants were collected by centrifugation at 500 g for 5 min followed by centrifugation at 15000 g for 5 min. The levels of LDH and eotaxin levels were then measured using a LDH assay kit (Roche Diagnostics) and a Duoset ELISA kit (R&D systems), respectively.
Number of rats for NiO NPs was 10 per group, while the number of rats for NiCl2 and OVA-induced airway inflammation group was 4 per group. One-way analysis of variance (ANOVA) was applied to the data having more than 3 groups, while the unpaired student’s t-test was applied to the OVA-induced airway inflammation group and NiCl2 treated group. When ANOVA test showed statistical significance (p < 0.05), each group was compared using post-hoc Tukey’s pairwise comparisons. Pearson correlation test was applied to evaluate the correlation between the levels of LDH and eotaxin in cell lysis experiment. All statistical analysis and graphs were prepared using GraphPad Prism (version 6.0 for Windows; GraphPad Software, San Diego, CA, USA). A value of p < 0.05 was considered statistically significant.
ANOVA, analysis of variance; BALF, bronchoalveolar lavage fluid; BCA, bicinchoninic acid; BET, Brunauer, Emmett, and Teller; CINC-3, cytokine-induced neutrophil chemoattractant-3; CoCl2, cobalt chloride; CoO, cobalt monoxide; CuO, copper oxide; DW, distilled water; ELISA, enzyme-linked immunosorbent assay; Fe2O3, iron oxide; FE-SEM, field emission-type scanning electron microscopy; ICP-MS, inductively coupled mass spectrometry; IFN-γ, interferon-γ; IgE, immunoglobulin E; IL, interleukin; LAL, Limulus Amoebocyte Lysate; LDH, lactate dehydrogenase; Ni, nickel; NiCl2, nickel chloride; NiO, nickel oxide; NP, nanoparticle; OVA, ovalbumin; PBS, phosphate buffered saline; PM, particulate matter; ROS, reactive oxygen species; TEM, transmission electron microscopy; Th1-type, T helper type 1; TiO2, titanium dioxide; ZnCl2, zinc chloride; ZnO, zinc oxide
We thank Mr. Myeongsik Kim, Mr. Jiseok Kim, Ms. Ganghae Kwon, Ms. Yerim Kim, and Ms. Jina Kim for their assistance in the animal study.
This research was supported by the Korean Ministry of Food and Drug Safety (15182MFDS462).
Availability of data and supporting materials
Raw data files can be shared by the corresponding author upon request.
WSC provided key intellectual input in the concept and design of the study. SL performed experiment and contributed to the manuscript. SHH, DKL, and YSH measured the levels of intracellular eotaxin and Ni in BALF, and contributed to the manuscript. JJ (Jiyoung Jeong), YH and SHK performed the correlation study of LDH against eotaxin and contributed to the manuscript. HSL, STC, JJ (Jayoung Jeong), and CR provided expertise for analysis of data and contributed to the manuscript. All authors read and approved the final manuscript.
The authors declare they have no competing interests.
Ethics approval and consent to participate
All animal studies obtained proper ethics approval from the Institutional Animal Care and Use Committee in Dong-A University.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Hamelmann E, Tadeda K, Oshiba A, Gelfand EW. Role of IgE in the development of allergic airway inflammation and airway hyperresponsiveness--a murine model. Allergy. 1999;54(4):297–305.View ArticlePubMedGoogle Scholar
- Jarrett E, Bazin H. Elevation of total serum IgE in rats following helminth parasite infection. Nature. 1974;251(5476):613–4.View ArticlePubMedGoogle Scholar
- Szebeni J. Complement activation-related pseudoallergy: a stress reaction in blood triggered by nanomedicines and biologicals. Mol Immunol. 2014;61(2):163–73.View ArticlePubMedGoogle Scholar
- Cho WS, Duffin R, Poland CA, Duschl A, Oostingh GJ, Macnee W, et al. Differential pro-inflammatory effects of metal oxide nanoparticles and their soluble ions in vitro and in vivo; zinc and copper nanoparticles, but not their ions, recruit eosinophils to the lungs. Nanotoxicology. 2012;6:22–35.View ArticlePubMedGoogle Scholar
- Larsen ST, Roursgaard M, Jensen KA, Nielsen GD. Nano titanium dioxide particles promote allergic sensitization and lung inflammation in mice. Basic Clin Pharmacol Toxicol. 2010;106(2):114–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Szebeni J, Storm G. Complement activation as a bioequivalence issue relevant to the development of generic liposomes and other nanoparticulate drugs. Biochem Biophys Res Commun. 2015. doi:10.1016/j.bbrc.2015.06.177.PubMedGoogle Scholar
- Cho WS, Duffin R, Thielbeer F, Bradley M, Megson IL, Macnee W, et al. Zeta potential and solubility to toxic ions as mechanisms of lung inflammation caused by metal/metal oxide nanoparticles. Toxicol Sci. 2012;126(2):469–77.View ArticlePubMedGoogle Scholar
- Jeong J, Han Y, Poland CA, Cho WS. Response-metrics for acute lung inflammation pattern by cobalt-based nanoparticles. Part Fibre Toxicol. 2015;12:13.View ArticlePubMedPubMed CentralGoogle Scholar
- Huang KL, Lee YH, Chen HI, Liao HS, Chiang BL, Cheng TJ. Zinc oxide nanoparticles induce eosinophilic airway inflammation in mice. J Hazard Mater. 2015;297:304–12.View ArticlePubMedGoogle Scholar
- Gilbert B, Fakra SC, Xia T, Pokhrel S, Madler L, Nel AE. The fate of ZnO nanoparticles administered to human bronchial epithelial cells. ACS Nano. 2012;6(6):4921–30.View ArticlePubMedPubMed CentralGoogle Scholar
- Cho WS, Duffin R, Howie SE, Scotton CJ, Wallace WA, Macnee W, et al. Progressive severe lung injury by zinc oxide nanoparticles; the role of Zn2+ dissolution inside lysosomes. Part Fibre Toxicol. 2011;8(1):27.View ArticlePubMedPubMed CentralGoogle Scholar
- Cho WS, Duffin R, Bradley M, Megson IL, MacNee W, Howie SEM, et al. NiO and Co3O4 nanoparticles induce lung DTH-like responses and alveolar lipoproteinosis. Eur Respir J. 2012;39(3):546–57.View ArticlePubMedGoogle Scholar
- Horie M, Fukui H, Nishio K, Endoh S, Kato H, Fujita K, et al. Evaluation of acute oxidative stress induced by NiO nanoparticles in vivo and in vitro. J Occup Health. 2011;53(2):64–74.View ArticlePubMedGoogle Scholar
- Rushton EK, Jiang J, Leonard SS, Eberly S, Castranova V, Biswas P, et al. Concept of assessing nanoparticle hazards considering nanoparticle dosemetric and chemical/biological response metrics. J Toxicol Environ Health A. 2010;73(5):445–61.View ArticlePubMedGoogle Scholar
- Oynebraten I, Barois N, Hagelsteen K, Johansen FE, Bakke O, Haraldsen G. Characterization of a novel chemokine-containing storage granule in endothelial cells: evidence for preferential exocytosis mediated by protein kinase A and diacylglycerol. J Immunol. 2005;175(8):5358–69.View ArticlePubMedGoogle Scholar
- Pang L, Knox AJ. Regulation of TNF-alpha-induced eotaxin release from cultured human airway smooth muscle cells by beta2-agonists and corticosteroids. FASEB J. 2001;15(1):261–9.View ArticlePubMedGoogle Scholar
- Williams TJ. Eotaxin-1 (CCL11). Front Immunol. 2015;6:84.View ArticlePubMedPubMed CentralGoogle Scholar
- Baggiolini M, Dewald B, Moser B. Human chemokines: an update. Annu Rev Immunol. 1997;15:675–705.View ArticlePubMedGoogle Scholar
- Matthews AN, Friend DS, Zimmermann N, Sarafi MN, Luster AD, Pearlman E, et al. Eotaxin is required for the baseline level of tissue eosinophils. Proc Natl Acad Sci U S A. 1998;95:6273–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Kawaguchi M, Kokubu F, Kuga H, Tomita T, Matsukura S, Kadokura M, et al. Expression of eotaxin by normal airway epithelial cells after influenza virus A infection. Int Arch Allergy Immunol. 2000;122 Suppl 1:44–9.View ArticlePubMedGoogle Scholar
- Nakajima T, Yamada H, Iikura M, Miyamasu M, Izumi S, Shida H, et al. Intracellular localization and release of eotaxin from normal eosinophils. FEBS Lett. 1998;434:226–30.View ArticlePubMedGoogle Scholar
- Roy R, Kumar S, Verma AK, Sharma A, Chaudhari BP, Tripathi A, et al. Zinc oxide nanoparticles provide an adjuvant effect to ovalbumin via a Th2 response in Balb/c mice. Int Immunol. 2014;26(3):159–72.View ArticlePubMedGoogle Scholar
- Ban M, Langonne I, Huguet N, Guichard Y, Goutet M. Iron oxide particles modulate the ovalbumin-induced Th2 immune response in mice. Toxicol Lett. 2013;216(1):31–9.View ArticlePubMedGoogle Scholar
- Nygaard UC, Hansen JS, Samuelsen M, Alberg T, Marioara CD, Lovik M. Single-walled and multi-walled carbon nanotubes promote allergic immune responses in mice. Toxicol Sci. 2009;109(1):113–23.View ArticlePubMedGoogle Scholar
- Pope SM, Zimmermann N, Stringer KF, Karow ML, Rothenberg ME. The eotaxin chemokines and CCR3 are fundamental regulators of allergen-induced pulmonary eosinophilia. J Immunol. 2005;175:5341–50.View ArticlePubMedGoogle Scholar
- Moghimi SM. Cancer nanomedicine and the complement system activation paradigm: anaphylaxis and tumour growth. J Control Release. 2014;190:556–62.View ArticlePubMedGoogle Scholar
- Banda NK, Mehta G, Chao Y, Wang G, Inturi S, Fossati-Jimack L, et al. Mechanisms of complement activation by dextran-coated superparamagnetic iron oxide (SPIO) nanoworms in mouse versus human serum. Part Fibre Toxicol. 2014;11:64.View ArticlePubMedPubMed CentralGoogle Scholar
- Young MT, Sandler DP, DeRoo LA, Vedal S, Kaufman JD, London SJ. Ambient air pollution exposure and incident adult asthma in a nationwide cohort of U.S. women. Am J Respir Crit Care Med. 2014;190(8):914–21.View ArticlePubMedPubMed CentralGoogle Scholar
- Gowers AM, Cullinan P, Ayres JG, Anderson HR, Strachan DP, Holgate ST, et al. Does outdoor air pollution induce new cases of asthma? Biological plausibility and evidence; a review. Respirology. 2012;17(6):887–98.View ArticlePubMedGoogle Scholar
- Nordling E, Berglind N, Melen E, Emenius G, Hallberg J, Nyberg F, et al. Traffic-related air pollution and childhood respiratory symptoms, function and allergies. Epidemiology. 2008;19(3):401–8.View ArticlePubMedGoogle Scholar
- Gruzieva O, Bergstrom A, Hulchiy O, Kull I, Lind T, Melen E, et al. Exposure to air pollution from traffic and childhood asthma until 12 years of age. Epidemiology. 2013;24(1):54–61.View ArticlePubMedGoogle Scholar
- Hirshon JM, Shardell M, Alles S, Powell JL, Squibb K, Ondov J, et al. Elevated ambient air zinc increases pediatric asthma morbidity. Environ Health Perspect. 2008;116(6):826–31.View ArticlePubMedPubMed CentralGoogle Scholar
- Stopford W, Turner J, Cappellini D, Brock T. Bioaccessibility testing of cobalt compounds. J Environ Monit. 2003;5(4):675–80.View ArticlePubMedGoogle Scholar
- Bihari P, Vippola M, Schultes S, Praetner M, Khandoga AG, Reichel CA, et al. Optimized dispersion of nanoparticles for biological in vitro and in vivo studies. Part Fibre Toxicol. 2008;5:14.View ArticlePubMedPubMed CentralGoogle Scholar
- Layachi S, Rogerieux F, Robidel F, Lacroix G, Bayat S. Effect of combined nitrogen dioxide and carbon nanoparticle exposure on lung function during ovalbumin sensitization in Brown Norway rat. PLoS One. 2012;7(9):e45687.View ArticlePubMedPubMed CentralGoogle Scholar