Background
Asthma is a heterogeneous, chronic inflammatory, respiratory disease characterized by recurrent obstructive respiratory events in response to asthma “triggers” [
1,
2]. According to the World Health Organization (WHO), annually, hundreds of millions of people suffer from asthma, and over 180,000 people pass away across the world as a result of this condition. Nanotechnology has offered promising strategies for pharmaceutical and therapeutic development by providing such beneficial features as high biodegradability, biocompatibility, adaptability, and minimal toxicity [
3‐
5]. Accordingly, nanoparticles (NPs) have emerged as efficient carriers for several pharmaceutical agents due to their unique physicochemical properties and desirable performance characteristics [
6‐
8].
Clinical trials using NPs have identified some of the reasons underlying acute and chronic diseases and proposed ways to prevent and treat these diseases [
9]. The NPs are effective drug transporters given their potentiality to penetrate and remain active in the tissues, cells, and bloodstream [
10]. However, the harmful effects of NPs are equally important since they might induce tissue and cellular damage, inflammasome activation, and undesirable modifications [
11].
Titanium dioxide (TiO
2) and its nano-derivatives have a wide range of applications. In this regard, they can be utilized in semiconductors, solar cells, photocatalyst belts, and medicine, as well as in consumer products, including paints, deodorants, toothpastes, sunscreens, and food supplements [
12‐
14]. Nonetheless, it is imperative to also consider the risks induced by TiO
2 NPs given their harmful effects on the respiratory system and potentiality to augment allergic airway inflammation [
15]. This kind of inflammation is transmitted by a complex interplay among different Th2 cytokines, like IL-4, IL-5, and IL-13. The production of cytokines is of significant importance in the pathogenesis of asthma since they further stimulate B cells and eosinophilic inflammation while inhibiting Th1 response [
16,
17]. The Th2-mediated allergic asthma and its crosstalk with TiO
2 NPs suggest the role of underlying cellular machinery in inducing allergic airway inflammation.
In 2017, the European Chemicals Agency (ECHA) Committee for Risk Assessment (RAC) concluded to classify TiO
2 as a substance suspected of causing cancer through the inhalation route. The RAC classification was made based on the hazardous characteristics of this substance [
18]. Regarding this and concerning the growing trend in the production and application of TiO
2 NPs, there is a rising demand for identifying the consequences of TiO
2 NP exposure, especially with respect to allergic and inflammatory aspects. Therefore, the present study was conducted to characterize TiO
2 NPs and investigate their effects on lung tissue morphology, non-pulmonary tissue uptake, in vivo modulation of allergic pulmonary inflammation, and immune response. It was hypothesized that the inhalation of TiO
2 NPs would have hazardous effects and might aggravate OVA-induced allergic airway inflammation.
Materials and methods
Nanoparticles and their physicochemical properties
For the purpose of the study, TiO
2 NPs (AEROXIDE® P25; Sigma Aldrich, Saint Louis, MO) were utilized with a primary particle size of 21 nm. The measurement of the particles was accomplished by dynamic light scattering (DLS) on a Wyatt DynaPro Plate-Reader II (Wyatt Technology Europe GmbH, Dernbach, Germany) and a Malvern Zetasizer Nano-ZSP (Malvern Instruments GmbH, Herrenberg, Germany) in 96-well plates at room temperature. In this regard, the samples were irradiated with a laser (semiconductor laser with a λ of 830 nm [Wyatt] or a HeNe laser with a λ of 632.8 nm [Malvern]). Subsequently, the intensity fluctuations of the scattered light (detected at a backscattering angle of 156° [Wyatt] or 173° [Malvern]) were analyzed to obtain the autocorrelation function. The device software (Wyatt: DYNAMICS 7.1.9 or Malvern: Zetasizer Software 7.11) outputted the mean particle size using cumulant analysis and a size distribution using a regularization scheme by intensity or number. The mean hydrodynamic diameter was expressed as the log-normal distribution for the intensity or number density, and the dispersity,
p, was calculated using the following formula:
$$ (p)=\frac{\sigma }{\mu } $$
where
μ signifies the mean, and
σ represents standard deviation.
It was assumed that the suspension viscosity was similar to that of water, corrected for temperature. In addition, the suspension refractive index was considered to be equal to that of water (
n = 1.33). The refractive index of the NPs calculated as 2.4900 with the absorption of 0.01 was applied in the study. The characterization of the NPs was performed using the transmission electron microscopy (TEM). To this end, the NP suspensions were dried at room temperature on pioloform TEM grids and then analyzed with a Tecnai 12 FEI Biotwin TEM setup (Fig.
S1).
Animals
In line with the study objectives, nine-week-old female, wild-type, BALB/c-mice were obtained from the Janvier Labs (Le Genest-Saint-Isle, France) and kept in a 12-h dark/light cycle at 22 °C with laboratory food and tap water ad libitum. The mice were acclimatized for 2 weeks prior to initiating the study. All animal experiments were performed in strict accordance with the German animal protection laws under the approval of the appropriate governmental authority. In addition, every experimental procedure was carried out following the ethical regulations and the animal welfare protocols of the state of Saarland. In order to generate an ovalbumin (OVA) mouse model, the BALB/c mice were intraperitoneally sensitized to OVA (i.e., an allergen), along with aluminum hydroxide-adsorbed OVA (2 mg AlOH
3 with 20 μg OVA). On the other hand, the control animals received phosphate-buffered saline (PBS) on days 0 and 7. Afterward, the mice were subjected to OVA challenges on days 17, 18, 19, and 20 via the intranasal route (Fig.
S2).
In order to prepare the NPs, the treated TiO
2 NPs were dispersed in double distilled water (Milli-Q®), and the suspensions were ultrasonicated for 15 min to keep the maximum dispersed state. In the NPs groups, each of the BALB/c mice was intranasally treated with 25 μl TiO
2 NPs suspension (50 mg/mL) 1 h after OVA exposure on days 17 and 20 (Fig.
S2). To ensure the homogeneity of the suspension, the stock solutions were vortexed shortly before nasal installation for each mouse. Day 21 was considered the study endpoint. Prior to sacrificing the mice, they were weighed and prepared for pulmonary function testing. Subsequently, the bronchoalveolar lavage fluid (BALF) and some organs were isolated for the implementation of different experiments. Each of the three untreated (i.e., PBS/PBS, OVA/PBS, and OVA/OVA) and three treated groups (i.e., PBS/TiO
2/PBS, OVA/TiO
2/PBS, and OVA/TiO
2/OVA) consisted of 5 mice and 10 mice, respectively.
Lung function testing
The lung function analysis was performed in our lab and included a non-invasive measurement with conscious animals. Specific airway resistance (sRaw) was performed using a double-chamber head-out plethysmograph (DSI Buxco FinePointe NAM, MN, USA). In addition, the enhancement of doses (0, 12.5, 25, and 50 mg/mL) was accomplished using methacholine (MCh) via an aerosol nebulizer. In this regard, after inserting the mice in the device, they were granted an acclimation period of 5 min to calm down. The aerosol volume was amounted to 0.02 ml and delivered within 1 min. Different MCh concentrations were applied within an interval of 6 min (i.e., 3 min for response time and 3 min for recovery period).
Tissue sampling and inductively coupled plasma mass spectrometry measurements
After the implementation of airway resistance measurements, the BALB/c-mice were sacrificed by bleeding, and their organs were removed. The lungs were subjected to histological analysis, and BALF analysis was conducted for cell counts. In order to perform ICP-MS screening for titanium (47Ti), some portions of the main organs were cut, weighed, and dissolved in 5 mL concentrated ultrapure HNO3. Subsequently, a 4% (v/v) solution of ultrapure HCl was added to a final volume of 10 ml. After a few days, the samples were dissolved and analyzed at room temperature using the Agilent 7500cx (Agilent Technologies, Santa Clara, CA). In addition, scandium (45Sc) was used as an internal standard.
Staining and histological analysis
To assess the lung histopathology and airway inflammation, lung cryosections (10 μm) were prepared by means of a cryostat (CM1950, Leica, Germany). Lung tissue cryosections were stained with hematoxylin and eosin (H&E) and periodic acid Schiff (PAS) as previously described [
19,
20]. In the next stage, the sections were examined using the Zeiss Axio Imager M2 microscope (Carl Zeiss AG, Oberkochen, Germany). The number of goblet cells in the airways was counted manually after PAS staining under the same light microscope. Furthermore, immunofluorescence (IF) staining was performed with the Shandon Sequenza system (Thermo Scientific, MA, USA). The lung sections of every mouse were dried at room temperature for 15 min. To reduce the nonspecific cross-reactions, the sections were blocked with 5% donkey serum diluted in PBS. Afterward, they were incubated with primary antibodies (i.e., antimouse F4/80 [eBioscience, San Diego, CA], antimouse Ly6G [Abcam, Cambridge, UK], antimouse Siglec-F [eBioscience, San Diego, CA], and antimouse CD3ε [Biolegend, San Diego, CA]) for 1 h at 20 °C and then incubated overnight at 4 °C.
On the second day, the sections were rinsed twice with PBS and then incubated with secondary fluorescein-conjugated antibodies (donkey antirabbit IgG cyanine Cy3, donkey antirat IgG Cy5, and goat anti-Armenian hamster IgG Cy3) for 2 h at room temperature (all secondary antibodies were obtained from Jackson Immunoresearch, West Grove, PA). The cryosections were counterstained with 80 μL 4, 6-diamidino-2-phenylindole (DAPI; 0.5 μg mL− 1, Carl Roth, Karlsruhe, Germany) for 15 min, washed several times with PBS and once with double-distilled water, and mounted with Fluoroshield™ fluorescence mounting medium (Sigma-Aldrich, St Louis, MI). Additionally, fluorescence microscopy was performed by means of the Zeiss Axio Imager M2 microscope (Carl Zeiss AG).
Bronchoalveolar lavage fluid collection
For the collection of BALF, the trachea was exposed by a midline incision in the neck. Subsequently, 1 ml of ice-cold PBS (pH = 7.4) containing protease inhibitors was injected into the lungs through the trachea and withdrawn after 10 s as described previously [
21,
22]. In the following stages, the recovered fluid was centrifuged at 1200 rpm for 10 min at 4 °C, the supernatants were removed, and the pellets were resuspended in 0.5 mL PBS. To determine the total cell number, the cells were enumerated by means of a Neubauer cell counting chamber. Afterward, the cytospots were prepared and stained using the Diff-Quick (Medion Diagnostics AG) staining solution in order to discriminate and count the immune cells, including macrophages, neutrophils, eosinophils, and lymphocytes.
Enzyme-linked immunosorbent assay
After collecting blood samples from the sacrificed animals, they were centrifuged, and the obtained sera were stored at − 80 °C until analysis. Serum concentrations of total immunoglobulin (Ig) E were measured using the commercially available enzyme-linked immunosorbent assay (ELISA) kits (885,046,022, Invitrogen, Vienna, Austria). To determine the protein level in the homogenates, a Pierce BCA protein assay (23,227, ThermoFisher Science, Germany) was performed on the homogenized snap-frozen lungs. After adjusting the protein level in each sample, the ELISA was conducted to analyze the cytokine levels of IL-4 (DY404–05, R&D Systems Inc., USA), IL-5 (DY405–05, R&D Systems Inc., USA), IL-13 (DY413–05, R&D Systems Inc., USA), and interferon-gamma (IFN-γ) (DY485–05, R&D Systems Inc., USA) according to the manufacturer’s protocol.
Investigation of nanoparticle phagocytosis
The phagocytic ability of primary murine macrophages was analyzed in vitro. To this end, alveolar macrophages were isolated from the BALF of control BALB/c mice (without OVA neither TiO2 NPs). The samples were then grown as adherent cultures in RPMI 1640 medium containing 10% FBS and 1% penicillin/streptomycin in eight-chamber culture dishes at 37 °C. The macrophages were treated with 0.0125, 0.025, and 1 mg/mL freshly prepared TiO2 NP dispersions for 1, 2, 4, 8, and 24 h. Subsequently, they were fixed with ice-cold acetone and stained with DAPI. Several images were randomly generated using an epifluorescence microscope (Zeiss Axio Imager M2).
Scanning electron microscopy and energy-dispersive X-ray spectroscopy
The sections obtained from the heart, lung, brain, stomach, kidney, spleen, and liver were scanned for TiO2 NPs using an SEM-EDX electron microscope (FEI/Philips XL 30 FEG ESEM; Eindhoven, NL). Moreover, the macrophages in the BALF samples were first stained with Diff-Quick and then scanned for NPs with the same microscope. The tissues, fixed in 2.5% glutardialdehyde and dehydrated in an ascending series of ethanol, dried in 1,1,1,3,3,3-hexamethyldisilazane (Sigma-Aldrich; Taufkirchen, Germany), and coated with carbon, were also evaluated with this setup.
Statistical analysis
The data were presented as mean ± SEM. Statistical analyses were carried out in GraphPad Prism 5.02 (GraphPad Software, Inc., La Jolla, CA) using one-way ANOVA, followed by Tukey’s test (comparing all pairs of columns). A p-value less than 0.05 was considered statistically significant.
Discussion
Nanosize particles show greater deposition in the alveoli of individuals with asthma and chronic obstructive pulmonary disease (COPD), where they might induce response or exacerbate the disease [
26]. The TiO
2 has recently become part of our everyday lives [
27]; accordingly, this compound and its derivative NPs are widely used in technology and medicine [
27]. Moreover, TiO
2 NPs might be found in cosmetics, toothpaste, sunscreens, food supplements, and paints. These particles, when inhaled, have been classified as Group 2B carcinogen by the International Agency for Research on Cancer.
Mishra et al. [
15] reported that TiO
2 NPs increased allergic airway inflammation and Socs3 expression via the NF-kB pathway in a mouse model of asthma. Moreover, Kim et al. [
11] demonstrated inflammasome activation in asthmatic lungs after TiO
2 NP exposure, suggesting the probable contributive effect of targeting the inflammasome on controlling NP-induced airway inflammation. In a human study performed by Heller et al. (2018), the pigment-grade TiO
2 NPs were reported to be associated with chronic inflammatory degenerative diseases, when inhaled and ingested. The authors also demonstrated that pancreatic TiO
2 pigment nanocrystals could enter the bloodstream and were associated with type II diabetes mellitus [
9].
In line with previous reports, our results indicated that intranasal exposure to TiO
2 NPs increased the AHR measured during MCh administration in the OVA mouse model. In addition, TiO
2 NPs were found to enhance eosinophil infiltration in the lungs of asthmatic mice, compared to those in the controls. Eosinophil is well recognized as a major effector cell in the asthmatic airways. The significant elevation of eosinophils is reported to be associated with extreme allergic reactions [
28]. Our results also revealed a significant neutrophil influx in the non-allergic mice in comparison to that in the PBS controls.
Neutrophils and their products are the key mediators of the inflammatory changes observed in the airways [
29]. This neutrophilic influx is the essential feature of the inflammation reaction induced by TiO
2 NPs in the PBS control mice, therefore, high-dose TiO
2 NP inhalation may also have occupational consequences for non-asthmatics.
In addition, TiO2 NPs significantly increased the number of goblet cells and consequently mucus secretion in the OVA/TiO2/OVA mice, compared to that in the OVA/OVA ones. The significant increase in the serum levels of IL-4 and IL-13 in the OVA/TiO2/OVA group was indicative of a strong Th2 response to TiO2 NPs exposure. Nonetheless, no alterations were observed in IFN-γ levels; therefore, Th1 was not involved. The OVA-treated mice showed higher total IgE levels following exposure to TiO2 NPs; however, this increase was not significant.
Our findings are consistent with the published reports revealing several mechanisms to show the local effects of TiO
2 NPs on airway inflammation [
15,
30‐
33]. However, to date, limited research has addressed the biodistribution of TiO
2 NPs into different mice organs after intranasal administration. Therefore, the current study was conducted to describe the systemic uptake of TiO
2 NPs and their translocation into extrapulmonary organs. Our results indicated that intranasally administered TiO
2 NPs translocated through the lungs and accumulated in the organs (i.e., liver, spleen, kidney, brain, stomach, and heart) as examined by SEM-EDX and ICP-MS. These particles are small enough to pass through the respiratory tissues into the bloodstream to disseminate into distant organs [
34,
35]. In addition, the detection of TiO
2 NPs in the brain tissue was indicative of the ability of these particles to pass across the blood-brain barrier into the central nervous system following intranasal application, probably via the olfactory bulb by neuronal transport [
36,
37].
Moreover, the present study was the first of its kind describing the combination of in vitro and in vivo uptake of TiO
2 NPs by alveolar macrophages. Based on the evidence, the NPs have the ability to activate phagocytic cells, like macrophages, to take them up. The halos around the macrophages with less NPs precipitation, as well as the macrophage morphological changes, seem to be the result of phagocytic activity [
3]. This was supported by in vivo studies (using SEM) showing TiO
2 NPs inside the BALF-macrophages of NPs-treated mice. Our data also revealed the presence of TiO
2 NPs aggregates both inside and outside the cells at different time points. This supports the findings of our DLS measurements indicating the instability of TiO
2 NPs and their aggregation/agglomeration over time.
Generally, the inhalation of nanosized TiO2, in combination with OVA, aggravates asthmatic features. The asthmatic exacerbation induced by TiO2 NPs is mainly eosinophilic-mediated and enhanced by goblet cell hyperplasia, mucus hypersecretion, increased cytokine levels, and AHR. In view of the findings presented in this study, TiO2 NPs alone did not induce strong asthmatic features and inflammatory response in the healthy mice (i.e., non-asthmatics). However, the ability of these particles to translocate into different organs underscores the need for assessing the risk and harmful toxicological potential of these particles in human health. Our findings can provide implications for human health, particularly for asthmatic individuals. Based on our findings, it is recommended that the individuals suffering from asthma or other respiratory diseases (e.g., COPD) limit their exposure to TiO2 NPs products. These results carry important implications for occupational and environmental health policy, especially for pre-existing asthmatic populations and workers in industries exposed to TiO2 NPs products by various routes.
Conclusion
The present study involved the examination of the intranasal instillation of TiO2 NPs in BALB/c-mice with and without asthma-like airway inflammation. As our data indicated, TiO2 NPs did not remain stable over time and agglomerated rapidly; nevertheless, these agglomerates were still observed in alveolar macrophages. The OVA/TiO2/OVA mice had high levels of different Th2 cytokines (i.e., IL-4, IL-5, and IL-13). Moreover, intranasal exposure to TiO2 NPs in pre-OVA-challenged subjects was found to potentiate the exacerbation of eosinophilic-mediated asthma in the airways. The present study is the first description of pulmonary TiO2 NPs uptake by extrapulmonary organs in the context of asthma using SEM-EDX microscopy, followed by ICP-MS measurements.
In light of our findings, it could be concluded that TiO2 NPs have an aggravating effect in OVA-challenged mice by modulating the airway microenvironment toward a Th2 immune response. These particles may act as a magnifier of allergic airway diseases, such as asthma. Further investigations are required to better understand the toxicity associated with TiO2 NPs accumulation in organs. In addition, more studies are needed to investigate the effects of TiO2 NPs on other respiratory diseases.
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