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Abstract

In medicine, the use of silica nanoparticles (SiO₂ NPs) offers new perspectives in biosensor, drug delivery and cancer therapy. However, questions about potential toxic and deleterious effects of SiO₂ NPs have also been raised. The aim of this study was to investigate the induction of cytotoxicity, oxidative stress and apoptosis by SiO₂ NPs (size 15 nm) in human skin epithelial (A431) and human lung epithelial (A549) cells. SiO₂ NPs (concentration range 25–200 µg/ml) induced dose-dependent cytotoxicity in both types of cells, which was demonstrated by cell viability (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide) and lactate dehydrogenase leakage assays. SiO₂ NPs were also found to induce oxidative stress in a dose-dependent manner, indicated by depletion of glutathione and induction of reactive oxygen species (ROS) generation and lipid peroxidation. Quantitative real-time polymerase chain reaction analysis showed that following the exposure of cells to SiO₂ NPs, the messenger RNA level of apoptotic genes (caspase-3 and caspase-9) were upregulated in a dose-dependent manner. Moreover, activities of caspase-3 and caspase-9 enzymes were also significantly higher in both kinds of cells exposed to SiO₂ NPs. This study suggested that SiO₂ NPs induce cytotoxicity and apoptosis in A431 and A549 cells, which is likely to be mediated through ROS generation and oxidative stress.

Keywords

A549 cells A431 cells apoptosis ROS

Introduction

Nano-biotechnology provides opportunity for the development of new unique materials in the nanometer size range (1–100 nm) that can be applied to many potential applications in biological science. Silica nanoparticles (SiO₂ NPs) has been considered an ideal material for biomedical applications and is being widely explored as biosensor,¹ biomarker,² cancer therapy,³ DNA/drug delivery^4,5 and enzyme immobilization.⁶ Therefore, understanding the toxicity of SiO₂ NPs at the cellular level is crucial for rational design of this material for biomedical applications.

Nanoparticles could easily enter into human body via different routes such as inhalation, ingestion and dermal contact. Inhalation and dermal contact are very common exposure routes by which nanoparticles deposit in lung and skin inducing inflammation, fibrosis and cytotoxicity.⁷ To date, several studies provided ample evidence that SiO₂ NPs distributed in blood, lungs, kidneys, spleen, pancreas or other organs.^8
–10 In vitro studies have shown decreased cell viability and oxidative stress after exposure to SiO₂ NPs in human lung epithelial (A549) cells, human endothelial (EAHY926) cells, murine macrophages (RAW 264.7), human embryonic kidney (HEK293) cells, rat neuronal (PC12) cells and human liver (HepG2) cells.^11

–15 However, little is known about the toxic effects of SiO₂ NPs on human skin cells that represents the first level of exposure to the nanoparticles.

In this study, we investigated the induction of cytotoxicity, oxidative stress and apoptosis by SiO₂ NPs in human skin epithelial (A431) cells. To avoid cell type-specific response, we also used human lung epithelial (A549) cells for SiO₂ NPs toxicity studies. To achieve this objective, we determined the cytotoxicity by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT; cell viability) and lactate dehydrogenase (LDH) leakage assays in A431 and A549 cells exposed to different concentrations of SiO₂ NPs. We further measured the oxidative stress markers such as reactive oxygen species (ROS), glutathione (GSH) and lipid peroxidation (LPO) in response to SiO₂ NPs exposure. Quantitative real-time polymerase chain reaction (PCR) was employed to see the effects of SiO₂ NPs on the messenger RNA (mRNA) level of apoptosis genes (caspase-3 and caspase-9). Moreover, activities of caspase-3 and caspase-9 enzymes were also examined in both the types of cells against SiO₂ NPs exposure. Both A431, derived from human epidermoid carcinoma, and A549 cells, derived from human lung carcinoma, have been widely utilized in toxicological studies.^16

–20

Materials and methods

Silica nanoparticles

Silica (SiO₂) nanopowder (product no. 4850MR) was purchased from Nanostructured and Amorphous Materials, Inc. (Houston, Texas, USA). Physicochemical characterization of SiO₂ NPs utilized in the present study was reported in our previous publication.¹⁵

Chemicals

Fetal bovine serum (FBS), Dulbecco’s modified Eagle’s medium (DMEM), Hank’s balanced salt solution (HBSS), penicillin–streptomycin and trypsin were bought from Invitrogen Co. (Carlsbad, California, USA). GSH, MTT, 5,5-dithio-bis-(2-nitrobenzoic acid) (DTNB), 2,7-dichlorofluorescin diacetate (DCFH-DA), thiobarbituric acid (TBA) and trichloroacetic acid (TCA) were purchased from Sigma-Aldrich (St Louis, Missouri, USA). LDH, caspase-3 and caspase-9 enzymes assay kits were obtained from Bio-Vision Inc. (Milpitas, California, USA). All other chemicals used in this study were of the highest purity available from commercial sources.

Cell culture and nanoparticles exposure

Both A431 and A549 cells were obtained from American Type Culture Collection (ATCC) (Manassas, Virginia, USA). Both types of cells were used between passages 10 and 20. Cells were cultured in DMEM supplemented with 10% FBS and 100 U/ml penicillin–streptomycin at 5% CO₂ and 37°C. At 85% confluence, cells were harvested using 0.25% trypsin and were subcultured into 75 cm² flasks, six-well plates or 96-well plates according to selection of experiments. Cells were allowed to attach the surface for 24 h prior to nanoparticles treatment. SiO₂ NPs were suspended in cell culture medium and diluted to appropriate concentrations (25–200 µg/ml). The dilutions of SiO₂ NPs were then sonicated using a sonicator bath at room temperature for 10 min at 40 W to avoid SiO₂ NPs agglomeration prior to cells exposure. Selection of SiO₂ NPs dosage (25–200 µg/ml) and exposure time (72 h) was based on a preliminary dose–response study (data not shown).

Cell viability assay

Viability of A431 and A549 cells after exposure to SiO₂ NPs was assessed by MTT assay as described by Ahamed et al.¹⁸ In brief, 10,000 cells/well were seeded in 96-well plates and exposed to different concentrations (25–200 μg/ml) of SiO₂ NPs for 72 h. At the end of exposure, culture medium was removed from each well to avoid interference of SiO₂ NPs and replaced with new medium containing MTT solution in an amount equal to 10% of culture volume and incubated for 3 h at 37°C until a purple colored formazan product developed. The resulting formazan product was dissolved in acidified isopropanol. Furthermore, 96-well plate was centrifuged at 2300g for 5 min to settle down the remaining SiO₂ NPs. Then, a 100-μl supernatant was transferred to other fresh well of 96-well plate and absorbance was measured at 570 nm using a microplate reader (Synergy-HT, BioTek, Winooski, VT, USA).

LDH leakage assay

LDH is an enzyme widely present in cytosol, which converts lactate to pyruvate. When plasma membrane integrity is disrupted, LDH leaks into culture media and its extracellular level is elevated.²¹ LDH assay was carried out by the LDH-cytotoxicity assay kit (Bio-Vision) according to the manufacturer’s protocol. In brief, 10,000 cells/well were seeded in 96-well plates and exposed to different concentrations (25–200 µg/ml) of SiO₂ NPs for 72 h. At the end of exposure, 96-well plate was centrifuged at 2300g for 5 min to settle down the SiO₂ NPs present in the solution. Then, a 100-µl supernatant was transferred to a fresh well of 96-well plate that already contains 100 µl of reaction mixture from Bio-Vision kit and incubated for 30 min at room temperature. After incubation, the absorbance of solution was measured at 340 nm using a microplate reader (Synergy-HT, BioTek). LDH levels in the media versus the cells were quantified and compared with the control values according to the instruction of kit.

Determination of ROS

ROS level was determined in A431 and A549 cells exposed to different concentrations (25–200 μg/ml) of SiO₂ NPs for 72 h. The production of intracellular ROS was measured using DCFH-DA.²² The DCFH-DA passively enters the cell, where it reacts with ROS to form the highly fluorescent compound dichlorofluorescein. Briefly, 10 mM of DCFH-DA stock solution (in methanol) was diluted in culture medium without serum or other additive to yield a 100 µM working solution. At the end of exposure, cells were washed twice with HBSS. Then cells were incubated in 1 ml working solution of DCFH-DA at 37°C for 30 min. Cells were lysed in alkaline solution and centrifuged at 2300g for 5 min. A 200 µl supernatant was transferred to 96-well plate and fluorescence was measured at 485 nm excitation and 520 nm emission using a microplate reader (Synergy-HT, BioTek). The values were expressed as percentage of fluorescence intensity relative to control wells.

Preparation of crude cell extract

For the measurement of LPO, GSH and caspase enzymes, A431 and A549 cells were cultured in 75 cm² culture flask and exposed to different concentrations (25–200 µg/ml) of SiO₂ NPs for 72 h. After the treatment, cells were harvested in ice-cold phosphate buffer saline by scraping and washed with phosphate buffer saline at 4°C. The cell pellets were then lysed in cell lysis buffer (1× 20 mM Tris-HCl (pH 7.5), 150 mM NaCl, 1 mM Na₂EDTA, 1% Triton and 2.5 mM sodium pyrophosphate) as described in our previous publication.¹⁵ Following centrifugation (15,000g for 10 min at 4°C), the supernatant (cell extract) was maintained on ice.

LPO assay

LPO was estimated by measuring the formation of malondialdehyde (MDA) using the method of Ohkawa et al.²³ MDA is one of the end products of membrane LPO. Briefly, a mixture of 0.1 ml cell extract and 1.9 ml of 0.1 M sodium phosphate buffer (pH 7.4) was incubated at 37°C for 1 h. After incubation, the mixture was precipitated with 5% TCA and centrifuged (2300g for 15 min at room temperature) to collect supernatant. Then 1.0 ml of 1% TBA was added to the supernatant and placed in the boiling water for 15 min. After cooling to room temperature, absorbance of the mixture was taken at 532 nm and was converted to MDA and expressed as nanomole per milligram of protein using molar extinction coefficient of 1.56 × 10⁵ M⁻¹ cm⁻¹.

GSH assay

GSH level was quantified using Ellman’s method.²⁴ Briefly, a mixture of 0.1 ml of cell extract and 0.9 ml of 5% TCA was centrifuged (2300g for 15 min at 4°C). Then 0.5 ml of supernatant was added to 1.5 ml of 0.01% DTNB and the reaction was monitored at 412 nm. The amount of GSH was expressed as nanomole per milligram protein.

Total RNA isolation and quantitative real-time PCR analysis

Both A431 and A549 cells were cultured in six-well plates and exposed to different concentrations (25–200 μg/ml) of SiO₂ NPs for 72 h. At the end of exposure, total RNA was extracted using Qiagen RNeasy mini Kit (Valencia, California, USA) according to the manufacturer’s instructions. Concentration of the extracted RNA was determined using Nanodrop 8000 spectrophotometer (Thermo-Scientific, Wilmington, Delaware, USA), and the integrity of RNA was visualized on a 1% agarose gel using a gel documentation system (Universal Hood II, BioRad, Hercules, California, USA). The first strand of complementary DNA (cDNA) was synthesized from 1 μg of total RNA by reverse transcriptase using M-MLV (Promega, Madison, Wisconsin, USA) and oligo (dT) primers (Promega) according to the manufacturer’s protocol. Quantitative real-time PCR was performed by QuantiTect SYBR Green PCR kit (Qiagen) using an ABI PRISM 7900HT Sequence Detection System (Applied Biosystems, Foster City, California, USA). Overall, 2 ml of template cDNA was added to the final volume of 20 μL of reaction mixture. Real-time PCR cycle parameters included 10 min at 95°C followed by 40 cycles involving denaturation at 95°C for 15 s, annealing at 60°C for 20 s and elongation at 72°C for 20 s. The sequences of the specific sets of primer for caspase-3, caspase-9 and β-actin used in this study are given in our previous publication.¹⁸ Expressions of selected genes were normalized to the β-actin gene, which was used as an internal housekeeping control. All the real-time PCR experiments were performed in triplicate, and data were expressed as the mean of at least three independent experiments.

Caspase-3 and caspase-9 enzymes assay

Activities of caspase-3 and caspase-9 enzymes were measured using Bio-Vision assay kit. Crude cell extract was prepared as described above. This assay is based on the principle that activated caspases in apoptotic cells cleave the synthetic substrates to release free chromophore p-nitroanilide (pNA), which is measured at 405 nm. The pNA was generated after specific action of caspase-3 and caspase-9 on tertrapeptide substrates DEVD-pNA and LEHD-pNA, respectively.^18,25 The reaction mixture consisted of 50 µl of cell extract protein (50 µg), 50 µl of 2× reaction buffer (containing 10 mM dithiothreitol) and 5 µl of 4 mM DEVD-pNA (for caspase-3) or LEHD-pNA (for caspase-9) substrate in a total volume of 105 µl. The reaction mixture was incubated at 37°C for 1 h and absorbance of the product was measured using microplate reader (Synergy-HT, BioTek) at 405 nm according to manufacturer’s protocol.

Protein estimation

Protein content was estimated using a bicinchoninic acid protein assay kit (Pierce Biotechnology, Inc., Rockford, Illinois, USA).

Statistical analysis

Data presented in this study are mean ± SD of three identical experiments made in three replicate. Statistical significance was determined by one-way analysis of variance followed by Dunnett’s multiple comparison test. Significance was ascribed at p < 0.05. All analyses were conducted using the Prism software package (GraphPad Software, Version 5.0, GraphPad Software Inc., San Diego, California, USA).

Results

SiO₂ NP-induced cytotoxicity

Cytotoxicity of SiO₂ NPs in A431 and A549 cells was evaluated by MTT and LDH assays. MTT results showed that cell viability was reduced by SiO₂ NPs and degree of reduction was dose-dependent. Viability of A431 cell was decreased to 89%, 77%, 60% and 49%, while A549 cell viability reduction was 87%, 74%, 58% and 45% at the concentrations of 25, 50, 100 and 200 µg/ml, respectively (p < 0.05 for each; Figure 1(a)).

Figure 1.

SiO₂ NPs induced cytotoxicity in A431 and A549 cells. Cells were exposed to different concentrations (25–200 µg/ml) of SiO₂ NPs for 72 h. At the end of exposure, cytotoxicity was determined as described in the Materials and Methods section. (a) MTT assay and (b) LDH assay. Data represented are mean ± SD of three identical experiments made in three replicate. *Significant difference compared with the controls (p < 0.05 for each). LDH: lactate dehydrogenase; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide; SiO₂ NPs: silica nanoparticles.

We further observed that SiO₂ NPs-induced a dose-dependent LDH leakage in both the types of cells. LDH leakage in A431 cells was increased to 125%, 157%, 189% and 208%, while in A549 cells LDH leakage was increased to 129%, 164%, 194% and 223% for the concentrations of 25, 50, 100 and 200 µg/ml, respectively (p < 0.05 for each; Figure 1(b)). Moreover, a reverse linear correlation was observed between LDH leakage and cell viability in A431 (R ² = 0.9938) and A549 (R ² = 0.9972) cells (Figure 2).

Figure 2.

Correlation between cell viability and LDH leakage in A431 and A549 cells after 72 h exposure to 25, 50, 100 and 200 µg/ml of SiO₂ NPs. LDH: lactate dehydrogenase; SiO₂ NPs: silica nanoparticles.

SiO₂ NP-induced oxidative stress

The potential of SiO₂ NPs to induce oxidative stress was examined by measuring the ROS, LPO and GSH levels in A431 and A549 cells. We found that SiO₂ NPs induced intracellular production of ROS in dose-dependent manner (p < 0.05 for each; Figure 3(a)). The MDA level, an end product of LPO was significantly higher, while antioxidant GSH level was significantly lower in cells exposed to SiO₂ NPs in the concentration range of 25–200 µg/ml for 72 h (Figure 3(b) and (c)). Furthermore, an inverse linear correlation was observed between ROS and GSH (Figure 4) and a similar negative correlation was observed between ROS and cell viability (Figure 5).

Figure 3.

SiO₂ NPs induced oxidative stress in A431 and A549 cells. Cells were exposed to different concentrations (25–200 µg/ml) of SiO₂ NPs for 72 h. At the end of exposure, oxidative stress parameters were determined as described in the Materials and Methods section. (a) ROS, (b) LPO and (c) GSH. Data represented are mean ± SD of three identical experiments made in three replicate. *Significant difference compared with the controls (p < 0.05 for each). GSH: glutathione; LPO: lipid peroxidation; ROS: reactive oxygen species; SiO₂ NPs: silica nanoparticles.

Figure 4.

Correlation between ROS level and GSH level in A431 and A549 cells after 72 h exposure to 25, 50, 100 and 200 µg/ml of SiO₂ NPs. GSH: glutathione; ROS: reactive oxygen species; SiO₂ NPs: silica nanoparticles.

Figure 5.

Correlation between cell viability and ROS level in A431 and A549 cells after 72 h exposure to 25, 50, 100 and 200 µg/ml of SiO₂ NPs. ROS: reactive oxygen species; SiO₂ NPs: silica nanoparticles.

SiO₂ NP-induced apoptosis

It is well known that ROS generation leads to apoptotic cell death. We utilized quantitative real-time PCR to analyze the mRNA levels of two apoptotic genes (caspase-3 and caspase-9) in A431 and A549 cells exposed SiO₂ NPs at concentrations of 25, 50, 100 and 200 µg/ml for 72 h. Results showed that mRNA levels of caspase-3 and caspase-9 genes was upregulated in dose-dependent manner in both the types of cells due to SiO₂ NPs exposure (p < 0.005 for each; Figure 6). To support our hypothesis of apoptosis induction by SiO₂ NPs, we further examined the activities of caspase-3 and caspase-9 enzymes at the concentrations of 25, 50, 100 and 200 µg/ml. These results also demonstrated that SiO₂ NPs induced the activities of both the apoptotic enzymes in dose-dependent manner (p < 0.05 for each; Figure 7).

Figure 6.

SiO₂ NPs upregulated the mRNA levels of caspase-3 and caspase-9 genes in A431 and A549 cells. Cells were treated with different concentrations (25–200 µg/ml) of SiO₂ NPs for 72 h. Quantitative RT-PCR was performed by QuantiTect SYBR Green PCR kit using ABI PRISM 7900HT Sequence Detection System. The β-actin was used as the internal control to normalize the data. SiO₂ NPs-induced alterations in mRNA expression levels are expressed in relative quantity compared with those for the respective unexposed control cells. Data represented are mean ± SD of three identical experiments made in three replicate. *Statistically significant difference compared with the controls (p < 0.05 for each). RT-PCR: real-time polymerase chain reaction; SiO₂ NPs: silica nanoparticles; mRNA: messenger RNA.

Figure 7.

SiO₂ NPs induced the activities of caspase-3 and caspase-9 enzymes in A431 and A549 cells. Cells were treated with different concentrations (25–200 µg/ml) of SiO₂ NPs for 72 h. At the end of exposure, activities of caspase-3 and caspase-9 enzymes were determined using BioVision assay kit as described in the materials and methods section. (a) Caspase-3 and (b) caspase-9. Data represented are mean ± SD of three identical experiments made in three replicate. *Statistically significant difference compared with the controls (p < 0.05 for each).

Discussion

Physicochemical characterization of nanoparticles is an important aspect of nanotoxicity research. Characterization of present SiO₂ NPs was reported in our previous article.¹⁵ Briefly, SiO₂ NPs were highly pure, amorphous, smooth surface and spherical with an average diameter of 15 nm (transmission electron microscopy (TEM) size). The average hydrodynamic diameter of SiO₂ NPs in complete cell culture medium as determined by dynamic light scattering was around 96 nm. The higher size of SiO₂ NPs in aqueous suspension compared with TEM size might be due to the tendency of particles to agglomerate in aqueous state.¹⁵

SiO₂ NPs are being considered a potential candidate for biomedical applications because of their unique physicochemical properties. However, recent studies reported that SiO₂ NPs have a potential to induce toxicological effects to human health.^10,26

–29 These studies suggested that hazards have not been defined yet and more safety research is necessary. Therefore, we investigated the toxic response of SiO₂ NPs in human skin epithelial (A431) and lung epithelial (A549) cells. We found that SiO₂ NPs have a potential to induce cytotoxicity, oxidative stress and apoptosis in both the types of human cells.

Our MTT data showed that SiO₂ NPs-induced reduction in the viability of A431 and A549 cells in dose-dependent manner. LDH leakage from cells is another evidence for the penetration of nanoparticles into the cells and cell membrane damage.^14,30 It has been well documented that LDH levels in the cell medium elevated after the cells exposed to nanoparticles.^{18,19,31
–33} We also observed that LDH leakage was higher in a dose-dependent manner in both the types of cells treated with SiO₂ NPs. A significant reverse correlation between MTT and LDH was also observed. These results are in agreement with the results from other investigators showing a dose-dependent cytotoxicity induced by SiO₂ NPs in human embryonic kidney cells, human neuronal cells and human liver cells.^13
–15

Concomitant cellular oxidative stress was manifested by elevated oxidant levels and depleted antioxidant levels. In the present study, the oxidant (ROS and LPO) levels were higher, while the antioxidant (GSH) level was lower in A431 and A549 cells due to SiO₂ NPs exposure. Furthermore, negative linear correlation between the ROS and GSH indicated that free oxygen radical species were generated by exposure to SiO₂ NPs, which reduced intracellular antioxidant GSH levels. There was also a strong inverse correlation between decreased cell viability and increased ROS level. The inverse correlation between the decreased cell viability and the increased ROS level suggested that cell death could be the primary cause of ROS generation. Consequently, higher production of ROS leads to increased membrane LPO with a concomitant decrease in antioxidants such as GSH to scavenge these free oxygen radicals appears to be the underlying mechanisms of SiO₂ NPs toxicity.

ROS production and oxidative stress have received much attention in nanoparticles-induced apoptosis.^18,34
–36 ROS has been suggested to be signaling molecule for the initiation and execution of the apoptotic death program.³⁷ ^,38 We analyzed the mRNA expression of two apoptotic genes (caspase-3 and caspase-9) in response to SiO₂ NPs in A431 and A549 cells, because apoptosis is controlled through these pathways. Our quantitative real-time PCR results showed that SiO₂ NPs upregulated mRNA level of these genes. Furthermore, activities of caspase-3 and caspase-9 enzymes were also higher in SiO₂ NPs-treated cells. Taken together, ROS induces permeabilization of the outer mitochondrial membrane, which releases soluble proteins from the intermembrane space into the cytosol, where they promote caspase activation.^39,40 The best studied of these proteins is cytochrome c, which binds to apoptosis protease activating factor-1 (Apaf-1) and leads to the assembly of an apoptosome complex. This apoptosome binds to procaspase-9 and causes its auto-activation through a conformational change. Once initiated, caspase-9 goes on to activate caspase-3 (effector caspase), which cleaves substrates at aspartate residues and activation of this proteolytic activity appears to be an event in nanoparticle-induced apoptosis.^18,41 Apoptotic response of SiO₂ NPs in A431 and A549 cells are supported by our previous investigation, where SiO₂ NPs induced apoptosis in human liver cells (HepG2).¹⁵

In conclusion, we have shown that SiO₂ NPs produce significant cytotoxicity to A431 and A549 cells in dose-dependent manner in the concentration range of 25–200 µg/ml. This nanoparticle was also found to induce oxidative stress by inducing oxidants (ROS and LPO) and depleting antioxidant (GSH). Furthermore, mRNA levels and activities of casapase-3 and capase-9 enzymes were upregulated by SiO₂ NPs. It is also worth mentioning that A549 cells seem to be marginally more susceptible to SiO₂ NPs exposure than A431 cells. Taken together, this study suggesting that SiO₂ NPs may induce cytotoxicity and apoptosis in A431 and A549 cells, which is likely to be mediated through ROS generation and oxidative stress. Further studies are underway to examine the molecular mechanism of toxicity induced by SiO₂ NPs.

Footnotes

Conflict of interest

The authors declared no conflicts of interest.

Funding

This work was supported by King Abdulaziz City for Science and Technology under the National Plan for Science and Technology (Grant No.: 10-NAN1201-02).

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Salvesen

. Caspase substrates. Cell Death Differ 2007; 14: 66–72.

Silica nanoparticles-induced cytotoxicity,oxidative stress and apoptosis in cultured A431 and A549 cells

Abstract

Keywords

Introduction

Materials and methods

Silica nanoparticles

Chemicals

Cell culture and nanoparticles exposure

Cell viability assay

LDH leakage assay

Determination of ROS

Preparation of crude cell extract

LPO assay

GSH assay

Total RNA isolation and quantitative real-time PCR analysis

Caspase-3 and caspase-9 enzymes assay

Protein estimation

Statistical analysis

Results

SiO2 NP-induced cytotoxicity

SiO2 NP-induced oxidative stress

SiO2 NP-induced apoptosis

Discussion

Footnotes

Conflict of interest

Funding

References

SiO₂ NP-induced cytotoxicity

SiO₂ NP-induced oxidative stress

SiO₂ NP-induced apoptosis