Mechanism of cell death induced by silica nanoparticles in hepatocyte cells is by apoptosis

Abstract

Silicon is one of the most widely used chemical materials, and the increasing use of silica nanoparticles (SNs) highlights the requirement for safety and biological toxicity studies. The damaging and adverse effects of SNs on human hepatocytes remain largely unknown, as do the mechanisms involved. In the present study, the mechanisms underlying SN-induced toxicity in the human hepatocyte cell line HL-7702 were investigated. An MTT assay revealed that following exposure to SNs in the concentration range of 25-200 µg/ml, the viability of HL-7702 cells decreased, and the viability decreased further with increasing exposure time. SNs induced a delay in the S and G2/M phases of the cell cycle, and also induced DNA damage in these cells. Western blot and flow cytometry analyses revealed that cell death was mediated by mitochondrial damage and the upregulated expression of a number of pro-apoptotic proteins. In conclusion, exposure to SNs led to mitochondrial and DNA damage, resulting in apoptosis-mediated HL-7702 cell death. The study provided evidence for the cellular toxicity of SNs, and added to the growing body of evidence regarding the potential damaging effects of nanoparticles, indicating that caution should be exercised in their widespread usage.

Introduction

Nanomaterials are ultrafine particle materials whose structural units are 1-100 nm in size (1). They have four basic characteristics: Volume, surface, quantum size, and quantum tunneling effects, providing them with the capacity to serve important roles in various fields, including magnetic, optical, electrical, biological and medical fields (2). As a novel tool, nanotechnology has enabled the widespread use of silica nanoparticles (SNs) in the biomedical field, including in drug delivery, imaging and other therapeutic applications (3). For example, the ability to modulate Janus particle aggregation in response to a range of stimuli, in combination with the high resolution and deep penetration of multiwavelength photo-acoustic imaging, is attractive for a broad range of applications in diagnostic imaging and theranostics (4). The inherent low level of toxicity and small particle size enable SNs to enter the blood circulation and be used for drug administration and transportation in treatment protocols (5).

SNs are one of the most widely used nanopowder materials, with the highest yield in large-scale industrial production in the world (6). The use of SNs in the development of nanotechnology requires close monitoring of their toxicity and biological effects to ensure safe application. Human exposure to SNs through environmental, occupational and iatrogenic processes demands appropriate scrutiny to avoid the incidence of adverse effects (7,8). The safe use of SNs requires improved understanding of their interactions with cells, and their use in animal models provides the basis for toxicity assessments.

Although SNs, with low toxicity, serve a universal and important role in a variety of human processes and living organisms, they have the potential to accumulate in the organism (9). Long-term exposure to low-dose, or short-term exposure to higher-dose nanomaterials can lead to poisoning of the organism (10). Previous studies have reported that SNs exhibit the potential to induce cytotoxicity, oxidative stress and apoptosis in human cells (11,12). Inhalation and skin contact are common exposure routes via which SNs deposit in the lungs and on the skin, inducing inflammation, fibrosis and cytotoxicity (13). The cytotoxic effects of SNs arise due to oxidative stress and DNA damage (14). Our previous study revealed that SNs enter the human body via the respiratory system, acting on the cardiovascular system, lungs and other body tissues, inducing myocardial cytotoxicity or pulmonary fibrosis (15). One study found that 15‑ and 46‑nm SNs both significantly reduced the viability of bronchoalveolar carcinoma-derived cells compared to the control groups, in a dose- and time-dependent manner by causing oxidative stress (16). An animal study revealed that SNs injected intraperitoneally in mice were distributed in the brain, liver, heart and reproductive systems, and that toxicity varied in different organs (17). In addition to the established cardiovascular toxicity, pulmonary toxicity, reproductive toxicity and neurotoxicity have been observed (18,19); however, to what extent SNs affect other organs and tissues remains unclear.

Apoptosis is a common method of programmed cell death, characterized by depolymerization of the cytoskeleton, cell shrinkage, chromatin condensation, nuclear fragmentation and transport of phosphatidylserine to the cell surface (20). Its cytological features include nuclear condensation and DNA fragmentation (21). Nanoparticles can disrupt normal cellular function via cytotoxic stress, and are responsible for membrane damage (22). There are several genes and proteins reported to be involved in apoptotic pathways. Proteins of the Bcl-2 family comprise proapoptotic and antiapoptotic regulators of programmed cell death; the intended action mode of each component protein is to protect or destroy mitochondrial integrity, thereby activating or inhibiting the release of downstream factors, such as cytochrome C (Cyt C), thus resulting in the activation of caspase-3 (23). The Bcl-2/Bax ratio determines whether cell survival or apoptotic cell death occurs, and is an indicator of the strength of apoptosis (24). Detection of apoptosis using these common markers can increase the confidence and accuracy of assays. Another form of programmed cell death, autophagy, involves the clearing of damaged organelles to promote cell survival; however, whereas it is an emergency survival state, a complex interplay has been reported between autophagy and apoptosis in mammalian cells (25). Primarily, apoptosis represents cell death and autophagy cell survival, but it has been suggested that autophagy can precede, or even activate, apoptosis, by inducing the activation of caspases or the depletion of endogenous apoptosis inhibitors. SN-induced autophagy has been described previously and associated with the generation of reactive oxygen species (26), although whether SNs can induce apoptosis requires further investigation.

The liver is the most important detoxifying organ; it removes toxins from the circulation prior to excretion, and is the target organ for numerous poisons (27). Protecting the health of, and alleviating the burden on the hepatic system is a key focus in life science research. There is evidence that SNs can accumulate in the liver and cause severe damage following intravenous administration (28). Intranasal administration of SNs resulted in reduced levels in the blood compared with intravenous administration, but substantial quantities were still detectable in the liver, providing further evidence that SNs accumulate in the liver (29). Following intraperitoneal injection of mice with SNs, the nanoparticles distributed to the liver, heart, spleen, lung and kidney, inducing acute and chronic liver injury (17). Similar studies were also conducted in vitro, demonstrating that SNs can induce oxidative stress in HepG2 human liver cancer cells at 3 and 24 h following treatment, suggesting that an oxidative stress-mediated mitochondrial pathway, leading to apoptosis, may contribute to hepatotoxicity (30). In addition, Kupffer cells can be activated by SNs releasing bioactive mediators, such as reactive oxygen species (ROS), tumor necrosis factor-α and nitric oxide, which may also contribute to hepatotoxicity (31). TiO₂ nanoparticles were considered to induce apoptosis, hypothetically due to effective activation of caspases-3 and -9, downregulation of Bcl-2 gene and protein levels, upregulation of Bax and Cyt C protein, and promoted accumulation of ROS (32). There is substantial evidence that SNs can cause liver damage (33); however, the mechanisms via which hepatotoxicity occurs remain unclear.

In this study, the HL-7702 cell line was used as a model system to explore the SN- induced death of human hepatocytes and investigate the mechanisms involved. Increasing concentrations of SNs resulted in a significantly increased degree of cell death, which was determined to occur via apoptosis. SN exposure led to cell cycle arrest in the S and G2 phases and caused double-strand breaks (DSBs) in DNA. A decrease in the mitochondrial membrane potential (MMP) was also observed, indicating mitochondrial involvement in the induction of apoptosis. Upregulation of a variety of apoptotic mediators further suggested that SNs induced cell death via apoptosis.

Materials and methods

SNs

SNs, with a particle size of ~60 nm, were provided by the College of Chemistry at Shandong University. Briefly, 2.5 ml tetraethylorthosilicate was added to a premixed ethanol solution (50 ml) containing 2 ml of ammonia and 1 ml of water. The mixture was stirred (150 RPM) at 40°C for 12 h and was then centrifuged at 11,294 x g and 37°C for 15 min to isolate the particles. After washing with deionized water three times, the particles were dispersed in 50 ml of deionized water and sterilized by autoclaving (0.1 MPa, 120°C, 20 min) as a concentrated suspension for further experiments. SNs were dispersed in normal saline, which provided osmotic pressure comparable to that of cell fluid, sonicated with 20 KHz at 37°C for 10 min, and then, after standing for 24 h, the morphology, particle size and dispersibility of the particles were observed via transmission electron microscopy (magnification, x100,000; JEM‑2010; JEOL, Ltd.). Briefly, samples were prepared for TEM observation by dropping a 10-l ethanol solution of ultrasonic dispersed SNs onto a 400-mesh carbon-coated copper grid. Image-Pro Plus software 6.0 (Media Cybernetics, Inc.) was used to analyze the data and calculate the mean particle size. SNs were diluted (3 mg/ml) with saline following exposure to high pressure, and the particle size distribution and polymerization state were monitored by dynamic light scattering using a particle size analyzer after standing at room temperature for 24 h. The zeta potential and hydrodynamic size of the different concentrations of SNs in the dispersion medium (RPMI-1640; Gibco; Thermo Fisher Scientific, Inc.) were examined using a zeta-potential granulometer (Zeta Sizer 3000HS; Malvern Panalytical Ltd.).

Cell culture

Human normal hepatocyte HL-7702 cells were purchased from the Cell Resource Center, Shanghai Institutes for Biological Sciences (Chinese Academy of Sciences). HL-7702 cells were maintained in RPMI-1640 medium, containing 10% fetal bovine serum (Biological Industries) with 100 U/ml penicillin and 100 µg/ml streptomycin. Cells were incubated at 37°C in a 5% CO₂ humidified atmosphere and continuously passaged every 2-3 days. Cells were seeded in culture plates at a density of 1x10⁵ cells/ml for experiments. Following incubation for 24 h, cells were treated with SNs dispersed in serum-free RPMI-1640 at concentrations of 0, 25, 50, 100 or 200 mg/ml at 37°C for 24 h. Cells maintained in RPMI-1640 without SNs were used as the control group.

Cell viability

The effects of SNs on cell viability were determined using an MTT assay according to the manufacturer's protocols. following exposure to various SN concentrations in serum-free RPMI-1640 (0, 25, 50, 100, and 200 µg/ml) at a density of 5,000 cells/sample in a 96-well plate for 12 and 24 h, MTT was used to detect cell viability. Each group was set up in triplicate, and then 10 µl MTT solution (5 g/l) was added to each well and incubated for an additional 4 h at 37°C. The optical density (OD) was detected at 490 nm using a microplate reader (Thermo Fisher Scientific, Inc.). The following formula was used to determine cell viability: [(Ae-Ab)/(Ac-Ab)] x100%, where Ae is the experimental OD, Ac is the control OD, and Ab is the blank OD.

Hematoxylin and eosin (H&E) staining

H&E staining was conducted to observe cell morphology. The cells, after grouping, were seeded into six-well plates at a density of 1x10⁵ cells/sample. After exposure to SNs for 24 h, cells were washed 3 times with PBS. Following fixation with 95% ethanol at room temperature for 20 min, hematoxylin was used to stain the nuclei at room temperature for 3 min. After washing, the cytoplasm was stained with eosin at room temperature for 1 min. Cells were then washed, naturally dried and sealed with neutral balsam, and morphological changes were observed under an optical microscope (magnification, x200; DM4000M; Leica Microsystems GmbH).

Giemsa staining assay

Briefly, 1x10⁴ cells were inoculated onto clean and dry slides and exposed to SNs for 24 h. The cells were fixed in formaldehyde at room temperature for 15 min and then stained with Giemsa (Beijing Solarbio Science & Technology Co., Ltd.) at room temperature for 10 min, according to the manufacturer's protocols. After staining, the cells were observed under an optical microscope (magnification, x400). In general, apoptotic cells stained blue and were darker in color than normal or necrotic cells.

Annexin V‑FITC/propidium iodide (PI) apoptosis assay

Cells (1x10⁴ cells/sample) were stained by 5 µl Annexin V-FITC for 10 min and 5 µl PI for 5 min, respectively, at room temperature in the dark, according to the protocols provided by the manufacturer of an Annexin V-FITC/PI Apoptosis Assay kit (KGI Biosciences). The quantification of apoptosis induced by SNs in HL‑7702 cells was conducted via flow cytometry (FCM; BD Biosciences); cells were collected and evaluated using CellQuest software (version 5.0; BD Biosciences), and apoptosis was analyzed by ModFit software (version 3.2; Verity Software House). The results are expressed as the rate of apoptosis (the percentage of early + late apoptotic cells).

Membrane potential detection

Rhodamine 123 is a cationic fluorescent dye that penetrates cell membranes and is an indicator of the MMP. Cells (1x10⁴ cells/sample) were trypsinized with 0.25% trypsin for 2 min, then mixed with 20 µg/ml Rhodamine 123 and incubated at 37°C in the dark for 30 min. The MMP was detected via FCM (Beckman Coulter, Inc.), with an excitation wavelength of 488 nm and an emission wavelength of 525 nm. Cells were evaluated using CellQuest software (version 5.0).

DNA damage assay

Damage of DNA in HL-7702 cells following treatment with SNs was analyzed using a Comet Assay kit (Trevigen; Bio-Techne). Cultured cells (1x10⁵ cells/sample) were treated with SNs and harvested, and live cells were embedded within agarose on a glass slide. Cells were then lysed, and DNA was unwound under alkaline conditions, followed by electrophoresis (1%) and 20 µg/ml ethidium bromide staining. Damaged DNA migrates towards the anode, leading to the appearance of comets; DNA damage was quantified by calculating the ratio of the tail length to the head diameter. Single-cell gel electrophoresis (SCGE) analysis was used to determine whether DNA damage had occurred in HL-7702 treated with SNs.

Cell cycle assay

Cultured cells (1x10⁵ cells/sample) were trypsinized with 0.25% trypsin for 2 min, and centrifuged at 1,000 x g for 5 min at room temperature, then pre-cooled 70% ethanol was added to the cell pellet and stored overnight at 4°C. The cells were collected via centrifugation (1,000 x g) for 5 min at room temperature, following which 500 µl PI (Tianjin Sungene Biotech Co., Ltd.) was added, followed by FCM analysis. The results were analyzed using MultiCycle 6.0 (Phoenix Flow Systems, Inc.).

Immunocytochemistry

After fixing with 4% paraformaldehyde at room temperature for 15 min, cells were permeabilized with 0.5% Triton-X-100 for 20 min and blocked with 3% hydrogen peroxide for 30 min at room temperature to block endogenous peroxidase. Cells were blocked with 5% BSA (Beijing Solarbio Science & Technology Co., Ltd.) at room temperature for 30 min, followed by staining with primary and secondary antibodies, and then incubation for 10 min with DAB and 3 min with hematoxylin, both at room temperature. Immunocytochemistry was performed to detect the protein expression of Bax (1:500; cat. no. ab53154; Abcam), Bcl-2 (1:200; cat. no. ab59348; Abcam), Cyt C (1:1,000; cat. no. ab90529; Abcam) and caspase-3 (1:500; cat. no. ab13847; Abcam) using primary antibodies overnight at 4°C. The secondary antibody used was horseradish peroxidase (HRP)-conjugated goat anti-rabbit (1:1,000; cat. no. ab214880; Abcam) for 1 h at room temperature. After staining, the cells were observed under an optical microscope. Brown or yellow-stained cells were quantified for positive staining for each high‑power field (x400 magnification). Results are expressed as the total positive numbers of 50 random and continuous fields from each section using the software ImageJ (version 1.52; National Institutes of Health). All analyses were performed in a blinded manner without prior knowledge of the experimental groups.

Western blot assay

Western blotting was conducted to detect the expression of apoptosis-associated proteins. Following exposure to 0, 25, 50, 100 or 200 µg/ml SNs as aforementioned, cells were cultured at 37°C in a 5% CO₂ incubator and cultured for 24 h. Cells were washed with cold PBS 2-3 times and lysed in RIPA buffer (Beijing Solarbio Science & Technology Co., Ltd.) for 30 min on ice. Cells were then centrifuged for 10 min (8,430 x g at 4°C), and the supernatants were collected for protein determination using the BCA method (Beyotime Institute of Biotechnology). Protein samples (50 µg) were separated via SDS-PAGE (10% resolving gels, 5% stacking gels) and transferred to PVDF membranes (300 mA, 1.5 h). The membranes were blocked with 5% nonfat dry milk for 1 h at room temperature, followed by incubation with the aforementioned primary antibodies (at a dilution of 1:1,000 for Bax, 1:1,000 for Bcl-2, 1:2,000 for caspase-3 and 1:1,000 for Cyt C) and anti-GAPDH antibody (1:20,000; cat. no. 10494-1-AP, ProteinTech Group. Inc.) overnight at 4°C. After washing with TBS-0.05% Tween 20 (TBST), the membranes were incubated with HRP-conjugated goat anti-rabbit secondary antibodies (cat. no. ab6721; Abcam) at 1:10,000 dilutions for 1.5 h at room temperature, followed by a further wash with TBST, prior to exposure to an enhanced chemiluminescence reagent (ECL detection kit; Pierce; Thermo Fisher Scientific, Inc.). Finally, the membranes were exposed to an Odyssey CLx near-infrared fluorescence imaging system (LI‑COR Biosciences). Results were quantified using AlphaEaseFC software (version 4.0; ProteinSimple). All experiments were conducted in triplicate.

Statistical analysis

All statistical analysis was performed using Prism 5 (GraphPad Software, Inc.). Data are presented as the mean ± SEM. One-way ANOVA with Dunnett's post hoc test was used to compare across multiple treatments. Experiments were repeated three times with at least triplicate wells per condition. P<0.05 was considered to indicate a statistically significant difference.

Results

Characterization of SNs

As presented in Fig. 1 and Table I, SNs were spherical, with an average particle size of 60.80±4.36 nm, and good dry dispersion characteristics in the absence of aggregation. Zeta potential analysis revealed that different concentrations of SNs in serum-free RPMI-1640 medium were negatively charged, and the absolute value of the zeta potential was ~−20 eV, with good dispersion (Table II).

Figure 1.

Transmission electron microscopy of silica nanoparticles. Magnification, x100,000.

Table I.

Characterization of silica nanoparticles.

Characterization	Silica nanoparticles (60 nm)
Size and distribution (nm, mean ± SD)	60.80±4.36
Hydrodynamic size in normal saline (nm)	99.5
Shape	Spheroidicity

Table II.

Zeta potential of silica nanoparticles in RPMI-medium (n=5).

Concentration (µg/ml)	Zeta potential (eV)
25	−18.40±1.79
50	−23.29±1.70
100	−18.24±0.76
200	−22.75±1.00

Effects of SNs on cell viability

A decrease in viability was observed for HL-7702 cells that were exposed to SNs for 12 h, with a significant difference emerging at 200 µg/ml compared with the control (P<0.05; Fig. 2). Cell viability decreased further with increasing exposure time (24 h), specifically at the concentrations of 50-200 µg/ml (P<0.05), with decreases in cell viability at 100 and 200 µg/ml of 24.6±4.3 and 44.5±0.09%, respectively. These results indicated that SNs reduced the viability of HL-7702 cells.

Figure 2.

Viability of HL-7702 human hepatocytes. Cells were treated with 25, 50, 100 or 200 µg/ml SN solutions, or control treatment without SNs, for 12 and 24 h. ^*P<0.05 vs. control. SN, silica nanoparticle.

Effects of SNs on cell morphology

A number of morphological changes were observed following incubation of HL-7702 cells with SNs for 24 h. The control group resembled polygons with large and round nuclei, located in a central nucleus with well‑defined nucleoli; conversely, following treatment with 50 µg/ml SNs, cell swelling was evident and nuclei were mildly vacuolated (Fig. S1). With an increase in dose, the cell volume decreased, changes to the cytoplasm and nuclear vacuoles were notable, the chromatophore basophilic edge set was enhanced, the cytoplasm was dense, the eosinophilicity was enhanced and apoptotic bodies formed. At the highest concentration (200 µg/ml), nuclear membrane thickening, cell body shrinkage, nuclear pyknosis and disintegration were evident, indicating the occurrence of apoptosis (Fig. S1E). In summary, cells treated with SNs exhibited morphological changes associated with apoptosis.

Morphological changes in HL‑7702 cells indicating apoptosis caused by SNs

Giemsa staining was employed to detect apoptosis in HL-7702 cells treated with SNs. In cells stained with Giemsa, nuclei are stained blue or purple-blue, and the cytoplasm is stained pink under a light microscope (34). In the present study, normal nuclei stained purple-blue and exhibited uniform color following Giemsa staining (Fig. S2). Conversely, there was nuclear hyperchromatism, shrinkage, edge aggregation and the formation of densely stained apoptotic bodies in the SN treatment groups. As presented in Fig. S2, with increasing concentrations of SNs, the number of cells was reduced, cells shrunk, the intercellular space increased, the cell volume decreased, the cytoplasm permeability disappeared, the cell surface became prominent and apoptotic body formation was evident.

Flow cytometric analysis of SN‑induced apoptosis in HL‑7702 cells

Annexin V-FITC/PI double staining and a flow cytometer were used to detect apoptosis. A significant increase in apoptosis was observed at concentrations of SNs of 50-200 µg/ml, varying between 25-40% apoptosis by 24 h (P<0.05; Fig. 3F).

Figure 3.

Effects of SNs on the apoptosis of HL-7702 cells. (A) Cells exposed to basal medium without SNs for 24 h were observed. Cells exposed to (B) 25, (C) 50, (D) 100 and (E) 200 µg/ml of SNs were analyzed via flow cytometry. (F) Apoptotic rates of HL‑7702 cells treated with different concentrations of SNs for 24 h as determined using a flow cytometer. ^*P<0.05 vs. control. PI, propidium iodide; SN, silica nanoparticle.

Effects of SNs on the MMP

As a dose-dependent increase in apoptosis was observed following exposure to SNs, Rhodamine 123 was used to monitor the MMP in treated cells. Exposure of HL‑7702 cells to SNs for 24 h induced a significant decrease in MMP at 25 µg/ml, which decreased further with increasing concentrations of SNs (P<0.05; Fig. 4).

Figure 4.

Effects of SNs on the MMP of HL-7702 cells. Evaluation of the MMP of (A) control-treated HL-7702 cells, and cells treated with (B) 25, (C) 50, (D) 100 and (E) 200 µg/ml SNs for 24 h. The vertical axis indicates the number of cells and the horizontal axis indicates the MMP. (F) Quantification of the effects of SN treatment on the MMP as determined via flow cytometry. ^*P<0.05 vs. control. MMP, mitochondrial membrane potential; RHO, Rhodamine 123; SN, silica nanoparticles.

Treatment with SNs induces DNA damage

SCGE and an alkaline comet assay were used to determine the levels of DSBs in cultured HL-7702 cells treated with various concentrations of SNs. Whereas control cells appeared to be largely spherical, cells treated with different concentrations of SNs exhibited cell trailing or tail formation, indicating the formation of DSBs, which increased with the concentration of SNs (Fig. 5).

Figure 5.

DNA damage in HL-7702 cells treated with SNs. Evaluation of DNA damage in (A) control-treated HL-7702 cells, and cells treated with (B) 25, (C) 50, (D) 100 and (E) 200 µg/ml SNs for 24 h. Cells were subjected to single-cell gel electrophoresis; cells possessing double-strand breaks exhibit comet-like tails during electrophoresis. (F) Quantification of the effects of SN treatment on DNA damage. ^*P<0.05 vs. control. SN, silica nanoparticle.

Effects of SNs on the cell cycle

FCM analysis revealed that HL-7702 cells treated with SNs exhibited a significantly decreased percentage of cells in G₀/G₁ phase after 24 h, whereas the S and G2/M phase proportions significantly increased (Fig. 6). These results indicated that, following exposure to SNs, cells were impeded in their cycle progression and accumulated in the G2/M phase (Fig. 6F).

Figure 6.

Cell cycle arrest in HL-7702 cells treated with SNs. Cell cycle analysis of (A) control-treated HL-7702 cells, and cells treated with (B) 25, (C) 50, (D) 100 and (E) 200 µg/ml SNs for 24 h. (F) Quantification of the effects of SN treatment on the cell cycle distribution as determined via flow cytometry. ^*P<0.05 vs. control. SN, silica nanoparticles.

Effects of SNs on Bcl‑2, Bax, Cyt C and Caspase‑3 expression

It was demonstrated via immunocytochemistry that exposure of HL-7720 cells to increasing concentrations of SNs induced a significant increase in the number of Bax‑positive, Bcl-2-positive, Cyt C-positive and caspase-3-positive cells (P<0.05; Figs. 7A and S3-S6). Furthermore, western blotting revealed that SN treatment significantly increased Bax expression and decreased the Bcl-2/Bax ratio (P<0.05; Fig. 7B-D). The expression levels of Cyt C and caspase-3 were also significantly upregulated following treatment with increasing concentrations of SNs, compared with control group (P<0.05; Fig. 7C and D).

Figure 7.

Effects of SNs on apoptosis-associated protein expression in HL-7702 cells. (A) Effects of SNs on Bcl-2, Bax, Cyt C and Caspase-3 expression in HL-7702 cells, as determined by immunocytochemistry and diaminobenzidine staining. Cells were treated with 25, 50, 100, or 200 µg/ml SNs, or control treatment without SNs, for 24 h, and the percentage of cells exhibiting positive expression of the various proteins was determined. (B) Bcl-2/Bax ratio in cells treated with SNs as aforementioned. (C) Expression of Bcl-2, Bax, Cyt C and caspase-3 protein in cells treated as aforementioned, as determined by western blotting. (D) Western blot analysis of Bcl-2, Bax, Cyt C and Caspase-3 protein expression in HL-7702 cells treated as aforementioned. GAPDH was used as the internal control. ^*P<0.05 vs. control (n=5). Cyt C, cytochrome C; SN, silica nanoparticle.

Discussion

SNs are widely used in materials science, as catalysts and catalyst carriers, food additives and cosmetics, and particularly for biomedical applications, including in clinical diagnosis, as drugs and DNA carriers, and as biosensors (17). The aim of the present study was to investigate the effects of SNs on apoptotic cell death, and to determine the potential underlying mechanisms in HL-7702 cells in vitro. The study was designed to improve understanding regarding the effects of SNs on the human hepatic system and explore the potential mechanisms, to improve application safety.

Nanoparticles of different particle sizes have distinct biological and toxicological effects; it is generally accepted that the smaller the particle size, the greater the biological effects (35,36). In the present study, human hepatocytes were exposed to 60-nm particles with a zeta potential of ~−20 eV and good dispersion. A previous study reported that smaller particles (80 nm in diameter) entered cells more easily and induced more potent effects on the physiological functions of cells compared with larger particles (500 nm in diameter) (37). In addition, it has been demonstrated that the surface features of nanoparticles are major factors affecting their biological effectiveness (38,39), for example, small nanoparticles can be endocytosed by cells, resulting in cytotoxicity, whereas large aggregates adhere onto the cell surface and increase the growth rate of cells (40). Briefly, in the present study, SNs were spherical, with an average particle size of 60.80±4.36 nm, and with good dispersion; thus, the characteristics of the particles used in the present study were optimal for investigating the mechanisms underlying silica-induced toxicity using HL-7702 cells as an in vitro hepatic model system (41). In the present study, uniform size (60-nm) particles were used; nanoparticles of other diameters remain to be investigated. Previous studies have reported that, following intraperitoneal injection of an SN suspension in mice, nanoparticles were distributed to the liver, heart, spleen, lung, kidney and other tissues (15,17), and induced acute and chronic liver injury (42). The present study provided evidence that SNs were cytotoxic to the HL-7702 liver cell line, and that the mechanism of cell killing was predominantly via apoptosis.

In vivo experiments have indicated the hepatotoxicity of SNs. For example, acute liver failure occurred following long-term injection of 70-nm SNs in mice, and histological analysis confirmed accumulation in the liver (43). Furthermore, 30‑nm silica particles were also demonstrated to induce hepatotoxicity via in vivo experiments in mice (44). Additionally, a similar in vitro study reported that SNs induced apoptosis in a dose-dependent manner in HepG2 liver cancer cells (45). An additional in vitro study reported that SNs can penetrate cell membranes and deposit in organelles, altering protein expression and the outer MMP, and inducing cell cycle arrest, DNA damage and cell death (46). The present study corroborated these effects of SNs, as cell cycle arrest, DNA damage, a decrease in the MMP and apoptosis were observed in SN-treated HL-7702 cells.

In the present study, cell division was arrested in the G2/M phase following SN exposure, which was associated with reduced cell viability and the induction of cell death. Accumulating evidence indicates that manipulation of the cell cycle may prevent or induce an apoptotic response (47). The G2/M DNA damage checkpoint is an important cell cycle checkpoint in eukaryotic organisms ranging from yeast to mammals, ensuring that cells don't initiate mitosis until damaged DNA or incompletely replicated DNA is sufficiently repaired after replication (48). Cells that have a defective G2/M checkpoint enter mitosis before repairing their DNA, leading to apoptosis or death after cell division (49). When the cell receives a signal that it is not conducive to division, or the timing is immature, the cell will stop at the subsequent cell cycle checkpoint for examination; if an irreparable error is found, the cell initiates apoptosis (48). In the present study, it was determined that, following exposure to increasing concentrations of SNs, the cell cycle was arrested in the G2/M phase, potentially leading to the induction of apoptosis.

The MMP is generated by the asymmetric distribution of protons and other ions on the two sides of the mitochondrial inner membrane, and depolarization of the MMP is a specific and early marker of apoptosis (50). It occurs prior to the characteristic nuclear changes in apoptosis, such as chromatin condensation and DSBs (51). SNs may penetrate the cell membrane and remain in the mitochondria, leading to mitochondrial and cellular damage (52), suggesting that SNs may cause apoptosis via the mitochondrial pathway (3). This is consistent with the present findings, as a dose‑dependent disruption of the MMP was detected in SN-treated HL-7702 cells, potentially leading to the observed induction of apoptosis in these cells. Furthermore, progression to apoptosis is irreversible when the MMP collapses (53). A similar study has also observed that the loss of the MMP and disruption of the mitochondrial ultrastructure are associated with apoptosis, and that SNs can induce an increase in ROS, further exacerbating cellular toxicity (54).

Apoptosis involves multiple genes that strictly control the process, including the Bcl-2 and caspase families (55). In the present study, the expression of both Bcl-2 and Bax was increased, inconsistent with the induction of apoptosis; however, the Bcl-2/Bax ratio decreased with increasing SN concentrations, indicating a proapoptotic state in cells (56). A decreased Bcl-2/Bax ratio has been shown to reduce cellular resistance to apoptotic stimuli, leading to apoptosis (57). When Bcl-2 expression is higher than that of Bax, it forms homodimers, and apoptosis is inhibited. When Bax expression is higher than that of Bcl-2, Bax-Bax homodimers are formed and apoptosis is promoted. When the HepG2 human hepatocyte cell line was treated with SNs, the mRNA and protein expression levels of proapoptotic genes were upregulated, whereas anti-apoptotic genes, such as Bcl-2, were downregulated, resulting in the induction of apoptosis in a dose-dependent manner (21), consistent with the present study in HL-7702 cells.

In conclusion, it was revealed that SNs induced apoptosis in HL-7702 cells, potentially via the release of Cyt C from mitochondria and activation of caspase 3, and changes in the expression of apoptosis-associated proteins in the mitochondrial signaling pathway. SNs increased the protein expression of Bax and Bcl-2 in HL-7702 cells, but decreased the Bcl-2/Bax ratio. The present study only focused on one SN particle size and one signaling pathway; whether SNs can induce apoptosis via other pathways, such as receptor-mediated or endoplasmic reticulum pathways, remains to be investigated in future studies.

Abbreviations

SNs

silica nanoparticles

Cyt C

cytochrome C

ROS

reactive oxygen species

DSB

double strand breaks

H&E

hematoxylin and eosin

FCM

flow cytometry

MMP

mitochondrial membrane potential

SCGE

single-cell gel electrophoresis

Funding

The present study was funded by National Natural Science Foundation of China (grant nos. 81573198, 81602893 and 81872575), the Natural Science Foundation of Shandong Province (grant nos. ZR2015YL049 and ZR2018MH036), the Natural Science Foundation of Jiangsu Province (grant no. BK20140573], the Medical and Health) Technology Development Plan Project of Shandong Province (grant no. 2016WS0540), the Key Research and Development Plan of Shandong Province (grant nos. 2017GSF18186, 2017GSF18142 and 2018GSF118018) and the Innovation Project of Shandong Academy of Medical Science.

Availability of data and materials

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

Authors' contributions

YY, XJD, QW, JWL and ZJD conceived and designed the study. YY, XJD, LLS, EGZ and XY performed the experiments. YY and XJD drafted the paper. CP, AJY, HS and MFL designed the study, analyzed the data, and critically reviewed and edited the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.