Sage Journals: Discover world-class research

Abstract

Nanosized titanium dioxide (nano-TiO₂) is widely used in the chemical, electrical, and electronic industries. Nanosized TiO₂ has been reported to be an efficient photocatalyst, which is able to produce reactive oxygen species (ROS) under UVA irradiation. In the present work, we evaluate the effect of mitochondrial respiratory chain on the generation of ROS and cytotoxicity in keratinocyte (HaCaT) cells induced by nano-TiO₂ under UVA irradiation. HaCaT cells were pretreated with different inhibitors of mitochondrial respiratory chain and followed by treatment with 200 µg/mL nano-TiO₂, then exposed to UVA (365 nm) for 1 hour and cultured for 24 hours. Our results demonstrated that the complexes I and III of the mitochondrial respiratory chain are the major site in the ROS generation induced by nano-TiO₂. Our results also demonstrated that the uncouplers of mitochondrial oxidative phosphorylation resulted in obvious changes in the production of intracellular ROS induced by nano-TiO₂. The ROS sources of lipoxygenase, cyclooxygenase, and nicotinamide adenine dinucleotide phosphate oxidase had no significant effect on the ROS production. To some extent, nitric oxide synthase had effect on the ROS production. These results indicated that mitochondrial respiratory chain may be the main source of intracellular ROS production induced by nano-TiO₂.

Keywords

nanosized titanium dioxide mitochondrial respiratory chain reactive oxygen species HaCaT cells UVA irradiation.

Introduction

Among the various nanomaterials, nanosized titanium dioxide (nano-TiO₂) is chemically inert, noncorrosive, and photocatalytic, thus, nano-TiO₂ has been widely applied in consumer products, pigments,¹ photocatalysts,² and cosmetic products.³ For this reason, toxicological properties of nano-TiO₂ have been studied with several routes of exposure, including dermal, oral, and pulmonary exposures. Nano-TiO₂ showed toxicity in many animal organ types, including lung,^4,5 kidney,⁶ liver,⁷ and brain.⁸ It has been demonstrated that reactive oxygen species (ROS) generation is responsible, at least in part, for the toxicity of nano-TiO₂, which resulted in an inflammatory response.^9
–11 The role of cellular ROS induced by nano-TiO₂ has gained much attention, but the exact mechanism was not fully described.

Mitochondria are a source of ROS from superoxide anion formed along electron transfer in the respiratory chain. It is converted into hydrogen peroxide (H₂O₂) by superoxide dismutase (SOD), and consecutively, H₂O₂ turns into water by glutathione peroxidase and catalase. It has been demonstrated that nano-TiO₂ is able to induce an increase in ROS production and cause damage to DNA in human lung cells¹² and to induce micronucleus formation in human epidermal cells.¹³ Nano-TiO₂ reduces the glutathione content,¹³ increases lipid peroxidation, and decreases SOD levels.¹⁴ Even though nano-TiO₂ is not internalized into mitochondria, there is an increasing evidence for the alterations induced in mitochondria, including cytochrome c release from mitochondria to cytosol, changes in mitochondrial membrane permeability, and a decrease in mitochondrial membrane potential.¹⁴

Thus, based on the hypothesis that exposure of cells to nano-TiO₂ may impair mitochondria, the present study was designed to investigate the effect of the role of mitochondrial respiratory chain in the generation of ROS induced by nano-TiO₂. Furthermore, the sites in the ROS generation induced by nano-TiO₂ was also examined.

Materials and Methods

Nano-TiO₂ and Reagents

Nano-TiO₂ (P25, 25% rutile, and 75% anatase) with 21 nm was purchased from Degussa GmbH (Germany). The particle sizes and distribution of nano-TiO₂ were measured by Tecnai G2 20 transmission electron microscope (FEI, Holland). Crystal structure was characterized by X’Pert Prox X-ray diffraction instrument (FEI). HaCaT cells were purchased from China Center for Type Culture Collection (China). Rhodamine 123, 2′,7′-dichlorofluorescein diacetate (DCFH-DA) and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) were purchased from Sigma (St. Louis, MO). Modified Eagle medium (MEM), penicillin–streptomycin, and fetal bovine serum (FBS) were obtained from Hyclone Laboratories Inc. All other chemicals were of the highest grade that could be obtained commercially.

Preparation Suspension of Nano-TiO₂

Nano-TiO₂ was suspended in the cell culture medium and dispersed using a sonifier cell disruptor equipped with a microprobe for 10 to 15 minutes to produce the suspension. In each study, the suspension was freshly prepared and then immediately applied to human keratinocyte (HaCaT) cells.

Cell Culture and Exposure to Nano-TiO₂

HaCaT cells were grown in MEM supplemented with 10% FBS in the presence of 5% CO₂ in air at 37°C. Cells were incubated up to approximately 24 hours and grown to about 80% confluence before experiments. Rotenone (ROT, 10 μmol/L), thenoyltrifluoroacetone (TTFA, 25 μmol/L), antimycin A (AA, 10 μmol/L), and sodium azide (NaN₃, 1 mmol/L) were used as inhibitors for complexes I, II, III, and IV, respectively. Diphenyleneiodonium (DPI) chloride (10 μmol/L) and Nω-nitro-l-arginine (l-NNA, 1.0 mmol/L) were used as inhibitors for nicotinamide adenine dinucleotide phosphate (NADPH) oxidase and endothelial nitric oxide synthase (eNOS). Nordihydroguaiaretic acid (NDGA, 10 μmol/L) and indomethacin (INDO, 10 μmol/L) were used as inhibitors of lipoxygenase (LOX) and cyclooxygenases (COX). Carbonyl cyanide m-chlorophenylhydrazone (CCCP, 2.0 μmol/L) was used as inhibitor for uncouplers of mitochondrial oxidative phosphorylation. Cyclosporin A (CsA) was used as inhibitor of mitochondrial permeability transition (MPT) pore. The inhibitors were dissolved in phosphate-buffered saline (PBS) and pretreated for 30 minutes; after treatment, the inhibitor was removed and cells were washed with PBS and replaced with culture medium, and some experiments included treatment with nano-TiO₂. All cells were irradiated with the UVA light for 1 hour and then cultured for 24 hours.

UVA Irradiation

UVA light was provided by a UV lamp (Shanghai Jinguang Instrument, China) with continuous emission spectrum with a peak at 365 nm. The UV intensity at 365 nm was determined using a UVA radiometer (Beijing Normal University, China). The UVA lamp had a fluence rate of 3.5 mW/cm² and is an appropriate substitute for UVA occurring in natural sunlight.¹⁵ As reference, 1 hour irradiation corresponds to an incident dose of UVA of 12.6 J/cm².

Measurement of Intracellular ROS

2′,7′-Dichlorofluorescein diacetate is a cell-permeable nonfluorescent probe that is cleaved by intracellular esterases and turns into the fluorescent dichlorofluorescein upon reaction with ROS. The level of ROS generation was determined by the concomitant increase in dichlorofluorescein fluorescence. After treatments, cells were treated with 10 μmol/L DCFH-DA for 30 minutes at 37°C. The cells were washed again with PBS and then sonicated in 300 μL 0.1% Triton X-100 (PBS, pH 7.4) on ice for 10 seconds. After incubation at 4°C for 10 minutes, the homogenates were centrifuged at 12,000 rpm for 30 minutes, and the supernatants were used for assay with excitation wavelength at 488 nm and emission wavelength at 525 nm.

Cell Viability Assay

The cytotoxicity of particles was determined using the MTT assay. Briefly, cells were seeded in 96-well culture plates at a density of 5 × 10³ cells/well; after treatment, cells were then washed and wells refilled with fresh culture medium containing 0.5 mg/mL MTT (M2003; Sigma-Aldrich). After 4 hours, the insoluble crystals were solubilized by dimethyl sulfoxide 150 µL/well, and the absorbance was read at 490 nm.

Measurement of Intracellular MDA

HaCaT cells (1 × 10⁵ mL⁻¹) were transferred to 24-well plates in 1 mL MEM and preincubated overnight. After preincubation, the cells were incubated at 37°C for 24 hours without or with 200 µg/mL nano-TiO₂. At the end of the treatment, cells were washed with PBS and homogenized in 300 µL 0.1% Triton X-100 (PBS, pH 7.4) through sonication on ice for 10 seconds. After incubation at 4°C for 10 minutes, the homogenates were centrifuged at 10,000 rpm for 10 minutes, and the supernatants were used for the assay. Malondialdehyde (MDA) content was measured with the MDA kit by a spectrophotometer (WFZ, UV-2102).

Measurement of Cell Death

Cell death was quantified by Evan blue. For 100% cell death, the culture was heated at 100°C for 5 minutes. The percentage of cell death in selected treatments was also verified by counting several hundred cells under a microscope.

Western Blot Analysis

Proteins from mitochondrial as well as cytosolic fraction (50 µg) were separated on 12.5% (wt/vol) sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The proteins were transferred on to nitrocellulose, blocked in Tris-buffered saline, 0.3% (wt/vol) Tween 20, and 3% (wt/vol) dried skimmed milk, and they were labeled with antibody against cytochrome c (1/1,000; Zymed Laboratories, South San Francisco) at 4°C overnight. After washing (3 times for 15 minutes) in block buffer, the membrane was incubated in rabbit antimouse horseradish peroxidase conjugate (1/5,000) in Tris-buffered saline/Tween 20 for 3 hours at room temperature and washed again. Labeling was detected by chemiluminescence.

Statistical Analysis

Statistical analyses were performed using Origin software (version 6.1; OriginLab). Experimental results were expressed as mean ± standard deviation (SD) for 3 different replicates at each test concentration. Statistical significance was established at P < 0.01.

Results

Characterization of Nano-TiO₂ Suspension

The morphology and size of nano-TiO₂ are shown in Figure 1A. There was no surface coating on nano-TiO₂. The size of nano-TiO₂ particles that were ultrasonicated ranged from 20 to 50 nm. The crystal structure of nano-TiO₂ is shown in Figure 1B, which was a mixture of anatase and rutile.

Figure 1.

Transmission electron micrographs and X-ray diffraction of nano-TiO₂ suspension. nano-TiO₂ indicates nanosized titanium dioxide.

Effects of Mitochondrial Respiratory Chain on the ROS Production Induced by Nano-TiO₂

The mitochondrial respiratory chain is a major source of ROS under pathological conditions. Oxidative stress is therefore implicated in cell injury, thereby causing inflammatory processes. As shown in Figure 2, the fluorescence in cells with nano-TiO₂ treatment significantly increased as compared with the control group. Pretreatment with ROT (Figure 2A) and AA (Figure 2B) increased the fluorescence by 32.26% and 22.69%, respectively, compared with the nano-TiO₂ group. On the contrary, our results also demonstrated that the fluorescence in cells pretreated with TTFA (Figure 2C) and NaN₃ (Figure 2D) alone was not altered.

Figure 2.

Effects of ROT (A), AA (B), TTFA (C), and NaN₃ (D) on intracellular ROS production induced by nano-TiO₂. Cells were treated with 200 µg/mL nano-TiO₂ only, or pretreated with ROT (10 μmol/L), AA (10 μmol/L), TTFA (25 μmol/L), and NaN₃ (1 mmol/L) for 30 minutes, respectively, followed by treatment with 200 µg/mL nano-TiO₂. Control received the culture medium only. All samples were irradiated with the UVA light for 1 hour and then cultured for 24 hours. Results are expressed as mean ± SEM of at least 4 different experiments. **P < 0.01 represents the comparison with the control group; ^# P < 0.05 and ^## P < 0.01 represent the comparison with the nano-TiO₂ group. AA indicates antimycin A; nano-TiO₂, nano titanium oxide; ROS, reactive oxygen species; ROT, rotenone; SEM, standard error of the mean; TTFA, thenoyltrifluoroacetone.

Effects of Uncouplers of Mitochondrial Oxidative Phosphorylation on the ROS Production Induced by Nano-TiO₂

To further study the effects of mitochondrial respiratory chain on intracellular ROS production induced by nano-TiO₂, CCCP was used as an inhibitor for uncouplers of mitochondrial oxidative phosphorylation. As shown in Figure 3, the fluorescence in cells was not altered significantly as compared with the control group. However, the fluorescence in cells of nano-TiO₂ pretreated with CCCP decreased by 32.26% compared with the nano-TiO₂ group.

Figure 3.

Effects of CCCP on intracellular ROS production induced by nano-TiO₂. Cells were treated with 200 µg/mL nano-TiO₂ only, or pretreated with CCCP (2.0 μmol/L) for 30 minutes, followed by treatment with 200 µg/mL nano-TiO₂. Control received the culture medium only. All samples were irradiated with the UVA light for 1 hour and then cultured for 24 hours. Results are expressed as mean ± SEM of at least 4 different experiments. **P < 0.01 represents the comparison with the control group; ^# P < 0.05 and ^## P < 0.01 represent the comparison with the nano-TiO₂ group. CCCP, carbonyl cyanide m-chlorophenylhydrazone; ROS, reactive oxygen species; nano-TiO₂, nanosized titanium dioxide; SEM, standard error of the mean.

Effects of NADPH Oxidase and NOS on the ROS Production Induced by Nano-TiO₂

Several intracellular sources contribute to the production of ROS, including NADPH oxidase, NOS, LOX, and xanthine oxidase.¹⁶ To test whether the NADPH oxidase and NOS were involved in the production of ROS in HaCaT cells induced by nano-TiO₂, HaCaT cells were preincubated with specific inhibitors of NADPH oxidase and NOS. During the addition of NADPH oxidase inhibitor, DPI chloride, the fluorescence in cells was not altered compared with the nano-TiO₂ group (Figure 4A). While addition of NOS inhibitor, Nω-nitro-l-arginine decreased the fluorescence by 12.23% compared with the nano-TiO₂ group (Figure 4B).

Figure 4.

Effects of DPI (A) and l-NNA (B) on intracellular ROS production induced by nano-TiO₂. Cells were treated with 200 µg/mL nano-TiO₂ only, or pretreated with l-NNA (1.0 mmol/L), DPI (10 μmol/L) for 30 minutes, respectively, followed by treatment with 200 µg/mL nano-TiO₂. Control received the culture medium only. All samples were irradiated with the UVA light for 1 hour and then cultured for 24 hours. Results are expressed as mean ± SEM of at least 4 different experiments. **P < 0.01 represents the comparison with the control group; ^# P < 0.05 and ^## P < 0.01 represent the comparison with the nano-TiO₂ group). DPI, diphenyleneiodonium chloride; l-NNA, Nω-nitro-l-arginine; nano-TiO₂, nanosized titanium dioxide; SEM, standard error of the mean.

Effects of Arachidonic Acid Metabolism on the ROS Production Induced by Nano-TiO₂

Reactive oxygen species are also generated by arachidonic acid metabolites, which are released from membrane phospholipids via the activity of cytosolic phospholipase A2.¹⁷ In this study, we describe recent studies concerning the generation of ROS by arachidonic acid metabolites. In particular, we have focused on the manner in which arachidonic acid metabolism via LOX and COX contributes to ROS generation. However, during the addition of LOX inhibitor, NDGA (Figure 5A) and COX inhibitor, INDO (Figure 5B), the fluorescence in cells was not altered compared with the nano-TiO₂ group.

Figure 5.

Effects of NDGA (A) and INDO (B) on intracellular ROS production induced by nano-TiO₂. Cells were treated with 200 µg/mL nano-TiO₂ only, or pretreated with NDGA (10 μmol/L), INDO (10 μmol/L) for 30 minutes, respectively, followed by treatment with 200 µg/mL nano-TiO₂. Control was received culture medium only. All samples were irradiated with the UVA light for 1 hour and then cultured for 24 hours. Results are expressed as mean ± SEM of at least 4 different experiments. **P < 0.01 represents the comparison with the control group; ^# P < 0.05 and ^## P < 0.01 represent the comparison with the nano-TiO₂ group. INDO, indomethacin; nano-TiO₂, nanosized titanium oxide; NDGA, nordihydroguaiaretic acid; ROS, reactive oxygen species; SEM, standard error of the mean.

Effects of ROT and AA on Cell Viability and MDA Content

Pretreatment with ROT (10 μmol/L) and AA (10 μmol/L) led to a significant (P < 0.01) loss of cell viability from 49.74% to 43.81%, 40.51% compared with cells treated with nano-TiO₂ alone (Figure 6A), whereas the MDA content was significantly increased from 0.9 to 1.44, 1.56, respectively (Figure 6B). The results also demonstrated that cell viability and MDA content were not significantly affected after treatment with ROT (10 μmol/L) or AA (10 μmol/L) alone under the conditions tested in this study.

Figure 6.

Effects of ROT and AA on cell viability (A) and MDA content (B) induced by nano-TiO₂. Cells were treated with 200 µg/mL nano-TiO₂ only, or pretreated with ROT (10 μmol/L), AA (10 μmol/L) for 30 minutes, respectively, followed by treatment with 200 µg/mL nano-TiO₂. Control received the culture medium only. All samples were irradiated with the UVA light for 1 hour and then cultured for 24 hours. Results are expressed as mean ± SEM of at least 4 different experiments. **P < 0.01 represents the comparison with the control group; ^# P < 0.05 and ^## P < 0.01 represent the comparison with the nano-TiO₂ group. AA indicates antimycin A; MDA, malondialdehyde; nano-TiO₂, nanosized titanium dioxide; ROT, rotenone; SEM, standard error of the mean.

Effects of CCCP and l-NNA on Cell Viability and MDA Content

Carbonyl cyanide m-chlorophenylhydrazone and l-NNA have been associated with ROS generation induced by nano-TiO₂, therefore, the cell viability and MDA content were examined. As shown in Figure 7A, the cell viability of HaCaT cells treated with nano-TiO₂ caused almost a 2-fold decrease as compared with the control. However, pretreatment with 2.0 μmol/L of CCCP induced a marked increase (P < 0.01) in cell viability from 49.74% to 82.8%. Pretreatment with 1.0 mmol/L of l-NNA increased the cell viability from 49.74% to 71.71% compared with nano-TiO₂ treatment alone (P < 0.01). Pretreatment with CCCP and l-NNA, the MDA content was decreased from 0.9 to 0.54, 0.46, respectively (P < 0.01; Figure 7B).

Figure 7.

Effects of CCCP and l-NNA on cell viability (A) and MDA content (B) induced by nano-TiO₂. Cells were treated with 200 µg/mL nano-TiO₂ only, or pretreated with CCCP (2.0 μmol/L), l-NNA (1 mmol/L) for 30 minutes, respectively, followed by treatment with 200 µg/mL nano-TiO₂. Control was received culture medium only. All samples were irradiated with the UVA light for 1 hour and then cultured for 24 hours. Results are expressed as mean ± SEM of at least 4 different experiments. **P < 0.01 represents the comparison with the control group; ^# P < 0.05 and ^## P < 0.01 represent the comparison with the nano-TiO₂ group. CCCP, carbonyl cyanide m-chlorophenylhydrazone; nano TiO₂, nanosized titanium dioxide; l-NNA, Nω-nitro-l-arginine; SEM, standard error of the mean.

Opening of Permeability Transition Pore and Release of Cytochrome c

One of the major molecular mechanisms that lead to profound changes in mitochondrial functioning is caused by an alteration in MPT, which protects the mitochondria from the loss of electrochemical potential for H⁺ by preventing nonspecific transfer of solutes of 1,500 D.¹⁸ To test the role of MPT in the oxidative stress induced by nano-TiO₂, we took advantage of the demonstrated inhibition of MPT by CsA. Staining the cells with Evan blue showed that CsA effectively reduced the amount of cell death from 64% to 33% (Figure 8A). The localization of cytochrome c in cells was studied by Western blotting. Cytosolic proteins from cells treated with nano-TiO₂ in the presence or absence of CsA were separated on 12.5% (wt/vol) SDS-PAGE and were probed with antibody against cytochrome c.¹⁹ Cyclosporin A effectively reduced the release of cytochrome c from mitochondria. However, CsA did not completely block the release of cytochrome c into the cytosol, and a small amount of cytochrome c was found also in the cytosol (Figure 8B).

Figure 8.

Effects of MPT pore in nano-TiO₂ induced cell death (A) and cytochrome c releasing (B) in HaCaT cells. Results are expressed as mean ± SEM of at least 4 different experiments. **P < 0.01 represents the comparison with the control group; ^## P < 0.01 represents the comparison with the nano-TiO₂ group. MPT, mitochondrial permeability transition pore; nano-TiO₂ nanosized titanium dioxide; SEM, standard error of the mean.

Discussion

Mitochondria are the main source for the generation of ROS.^1,20 More than 90% of the oxygen consumed by mammalian cells is utilized in mitochondria, and up to 4% of this oxygen is transformed into ROS.²¹ Dysfunction in electron transfer through the mitochondrial respiratory chain may result in the generation of ROS species such as superoxide anion radical (O₂ ^•), hydrogen peroxide (H₂O₂), and the hydroxyl radical (OH^•).^22,23 In most organisms, the mitochondrial respiratory chain contains the 4 classical components of the electron transport chain (complexes I, II, III, and IV), where the electron transport couples with translocation of protons from the mitochondrial matrix to the intermembrane space.^24,25 Complexes I and III in the electron transport chain are thought to be responsible for ROS production because O₂ ^• is formed from molecular oxygen (O₂) and then dismutated to H₂O₂ as electrons pass through the mitochondrial respiratory chain (ie, complexes I and III).²⁶ Mitochondrial electron transport is inhibited by the disappearance of metallothionein in human bronchial epithelial cells following exposure to silver nitrate. Nano-TiO₂ is usually present under 2 crystalline forms, anatase and rutile, that have a different photocatalytic power. The anatase crystal form is more photoreactive than the rutile one. The anatase–rutile mixture (consists of 75% anatase and 25% rutile, P25) is a widely used nano-TiO₂ in the world, which is applied in water treatment, self-cleaning windows, antimicrobial coatings and paints, and chemical industry. Owing to the existence of P25 in environment, skin is inevitable to become a potential target site. In our previous study, P25-induced cytotoxicity was evaluated using HaCaT cells. It was found that nano-TiO₂ (50-200 μg/mL) caused cytotoxicity through increasing ROS formation and matrix metalloproteinase collapse under UV irradiation. Ultraviolet irradiation, particularly UVA, has a capacity to generate ROS in cells; this may be due to the formation of ROS when TiO₂ is exposed to UV light.¹⁴ Notably, nano-TiO₂-induced cytotoxicity was prevented by antioxidants and ROS scavengers such as N-acetylcysteine, a sulfhydryl-containing antioxidant.²⁷ These findings suggest that mitochondria are the main target of nano-TiO₂-induced oxidative stress, and the mitochondrial respiratory chain plays an important role in the ROS generation induced by nano-TiO₂. Therefore, evaluating the direct effects of mitochondrial respiratory chain in the ROS generation induced by nano-TiO₂ seems to be important to better understand its mechanisms of cytotoxicity. Here, we observed the mitochondrial respiratory chain complexes I, II, III, and IV in the ROS generation by the addition of their inhibitors. Our results showed that cells pretreated with ROT (complexes I inhibitor) and AA (complexes III inhibitor) increased the ROS generation, whereas pretreatment with TTFA (complexes II inhibitor) and NaN₃ (complexes IV inhibitor) did not alter the ROS generation. Addition of CCCP, an inhibitor of uncouplers of mitochondrial oxidative phosphorylation, caused significant changes in ROS production. This reconfirms the role of the mitochondrial respiratory chain in the ROS generation induced by nano-TiO_2. Also, our findings about different effects of inhibitors on ROS production suggested that complexes I and III are main sites for superoxide production than complexes II and IV, which have been reported by others.^28,29 These may be that the inhibitor complexes I and III may have a role to induce an inflammatory response in primary cultured cells and complex II or IV may be not directly act on cells to induce inflammation, and mitochondrial-derived ROS production may be involved in inflammation response. In the murine microglial BV-2 cells model, the inhibition of mitochondrial respiratory chain Complex I and III indeed induced activation of p38, and NF-κB, which stimulatory effects were slightly more than complex II and the complex IV.²⁹

Besides mitochondrial respiratory chain, other possible sources contribute to the production of ROS, including endothelial arachidonic acid metabolism, NADPH oxidase, and NOS.¹⁶ Thus, the results of arachidonic acid metabolism, NADPH oxidase, and NOS on ROS generation induced by nano-TiO₂ were evaluated.

Arachidonic acid exerts a deleterious effect on mitochondria and ROS production.¹⁷ The manner in which arachidonic acid metabolism via LOX and COX has no effect on ROS generation. Furthermore, the addition of DPI, a specific inhibitor of NADPH oxidase, did not show any fall in ROS generation compared with that observed with sole pretreatment with nano-TiO₂, indicating that NADPH oxidase caused no significant changes in ROS generation.

Mitochondria have also been credited as a source of reactive nitrogen species derived from NO. Nitric oxide is generated enzymatically by a family of NOS, which includes neuronal NOS, eNOS, and inducible NOS.³⁰ All 3 NOS isoforms can also contribute to ROS production, since they have been shown to be susceptible to the “uncoupling” that leads to the formation of O₂ ⁻ (rather than NO).³¹ For eNOS, this process is triggered in vitro through the absence of the cofactors l-arginine and tetrahydrobiopterin. Uncoupling of eNOS has been demonstrated in the deoxycorticosterone acetate salt–induced hypertension.^32,33 However, others have demonstrated that vascular effects of eNOS uncoupling are due to the enhanced O₂ ⁻ production. Increased vascular ROS itself may induce eNOS uncoupling as a consequence of increased oxidation of tetrahydrobiopterin and inhibition of dimethylarginine dimethylaminohydrolase.³⁴ Our previous study showed the involvement of NO in ROS production and cytotoxicity in HaCaT cells induced by nano-TiO_2. ²⁷ In the present study, during the addition of NOS inhibitor, l-NNA decreased the ROS by 12.23% compared with the nano-TiO₂ treated alone. Purified NOS can produce O₂ ⁻ when the key NOS cofactor tetrahydrobiopterin (BH4) is oxidized to form dihydrobiopterin (BH2); phosphorylation of eNOS at serine 1177 increases O₂ ⁻ synthesis by the enzyme, whereas eNOS phosphorylation at threonine 495 does not.²⁶ These findings suggest that some of the effects of BH4 oxidation on NOS-dependent ROS synthesis may reflect changes in the NOS phosphorylation state.³⁵ Nitric oxide synthase-dependent O₂ ⁻ formation was first described in the studies of purified NOS proteins and was termed NOS “uncoupling,” because the usual catalytic electron flow within the enzyme is uncoupled from NO synthesis and is instead diverted to molecular oxygen to yield O2⁻.^34,36

In animal systems, it was shown that mitochondria are directly involved in the activation of cytosolic aspartate-specific Cys proteases (caspases) via release of cytochrome c.³⁷ The loss of cytochrome c from the inner mitochondrial membrane during apoptosis has been reported in many systems and is considered as a crucial regulatory step in apoptosis. At the early phases of apoptosis, the readdition of exogenous cytochrome c can markedly restore respiratory functions.³⁸ In Petunia (Petunia hybrida), the release of cytochrome c was found to be dispensable for the induction of a programmed cell death (PCD).³⁹ The increased cytochrome c following nano-TiO₂ treatment in the present study could promote caspase activation and apoptotic cell death.²⁰ Moreover, pretreatment with CsA attenuated both the rapid increase in apoptosis and membrane potential collapse following nano-TiO₂ administration. Therefore, it is possible to postulate that one or all of these events may be responsible for the toxicity and apoptosis of treatment with nano-TiO₂. Our result is in agreement with other reports suggesting that nano-TiO₂–induced ROS production leads to not only lipid peroxidation but also glutathione oxidation that could damage the mitochondrial membrane integrity and open the MPT pores.²⁷

Conclusion

In summary, we studied the effects of mitochondrial respiratory chain on the generation of ROS and cytotoxicity in HaCaT cells to extend our insights to the mechanisms of nano-TiO₂ toxicity. The experimental results suggest that mitochondrial respiratory chain may be the main source of intracellular ROS production induced by nano-TiO₂, the main sites were complexes I and III. The experimental results suggest that nano-TiO₂ induced mitochondrial oxidative stress and subsequently caused a gradual opening of MPT pore leading to the translocation of cytochrome c to the cytosol, terminating in PCD.

Footnotes

Authors’ Note

Guozhen Liu contributed equally to this work.

Author Contributions

Chengbin Xue contributed for the conception and design and for drafting the manuscript. Xiaonan Li and Guozhen Liu contributed for the conception and for critically revising the manuscript. Wei Liu contributed for analysis and for critically revising the manuscript. All authors gave final approval and agree to be accountable for all aspects of work ensuring integrity and accuracy.

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by Natural Science Foundation of Hubei Province (No. 2011CDB372), Wuhan Planning Project of Science and Technology (No. 2014070404010203). Project supported by the National Natural Science Foundation of China (Grant No. NSFC31470968) and Wuhan Middle-Aged and Young Backbone Personnel Training Project of Medicine.

References

Taavitsainen

Jalava

. Soft and harder multivariate modelling in developing the properties of titanium dioxide pigments. Chemometr Intell Lab Syst. 1995;29(2):307–319.

Sun

Meng

Loong

Hwa

. Removal of natural organic matter from water using a nano-structured photocatalyst coupled with filtrating membrane. Water Sci Technol. 2004;49(1):103–110.

Marta

Gabriela

Marcin

Wiesław

Wojciech

. Singlet oxygen generation in the presence of titanium dioxide materials used as sunscreens in suntan lotions. J Photochem. Photobiol. A. 2012;213(2-3):158–163.

Freyre-Fonseca

Delgado-Buenrostro

Gutierrez-Cirlos

. Titanium dioxide nanoparticles impair lung mitochondrial function. Toxicol Lett. 2011;202(2):111–119.

Liu

Zhao

J.F

. Biochemical toxicity of mice caused by nano-anatase TiO₂ particles. Biol Trace Elem Res. 2009;129(1-3):170–180.

Gui

Zhang

Zheng

. Molecular mechanism of kidney injury of mice caused by exposure to titanium dioxide nanoparticles. J Hazard Mate. 2011;195:365–370.

Palaniappan

Pramod

. Raman spectroscopic investigation on the microenvironment of the liver tissues of zebrafish (Danio rerio) due to titanium dioxide exposure. Vib Spectrosc. 2011;56(2):146–153.

Shin

Lee

Seo

Kim

Kang

Park

. Nanosized titanium dioxide enhanced inflammatory responses in the septic brain of mouse. Neuroscience. 2010;165(2):445–454.

Gonzalez

Lison

Kirsch

. Genotoxicity of engineered nanomaterials: a critical review. Nanotoxicology. 2008;2(4):252–273.

10.

Jaeger

Weissa

Jonas

Kriehuber

. Oxidative stress-induced cytotoxic and genotoxic effects of nano-sized titanium dioxide particles in human HaCaT keratinocytes. Toxicology. 2012;296(1-3):27–36.

11.

Yin

. Systematic influence induced by 3 nm titanium dioxide following intratracheal instillation of mice. J. Nanosci.Nanotechnol. 2010;10(12):8544–8549.

12.

Bhattacharya

Davoren

Boertz

. Titanium dioxide nanoparticles induce oxidative stress and DNA adduct formation but not DNA-breakage in human lung cells. Part Fibre Toxicol. 2009;6:17.

13.

Shukla

Sharma

Pandey

Singh

Sultana

Dhawan

. ROS-mediated genotoxicity induced by titanium dioxide nanoparticles in human epidermal cells. Toxicol In Vitro. 2011;25(1):231–241.

14.

Xue

Lan

. Nano titanium dioxide induces the generation of ROS and potential damage in HaCaT cells under UVA irradiation. J Nanosci Nanotechnol. 2010;10(12):8500–8507.

15.

Rampaul

Parkin

Cramer

. Damaging and protective properties of inorganic components of sunscreens applied to cultured human skin cells. J Photochem Photobiol A. 2007;191(2-3):138–148.

16.

Ruhul

Zarin

Katherine

. NADPH oxidase activity is required for endothelial cell proliferation and migration. FEBS Lett. 2001;486(3):252–256.

17.

Sang

. Inhibition of arachidonic acid and iron-induced mitochondrial dysfunction and apoptosis by oltipraz and novel 1,2-dithiole-3-thione congeners. Mol Pharmacol. 2009;75(1):242–253.

18.

Fortes

Castilho

Catisti

Carnieri

Vercesi

. Ca²⁺ induces a cyclosporin A-insensitive permeability transition pore in isolated potato tuber mitochondria mediated by reactive oxygen species. J Bioenerg Biomembr. 2001;33(1):43–51.

19.

Sun

Zhao

Hong

Zhai

. Cytochrome c release and caspase activation during menadione-induced apoptosis in plants. FEBS Lett. 1999;462(3):317–321

20.

Mashayekhi

Eskandari

Kobarfard

Khajeamiri

Hosseini

. Induction of mitochondrial permeability transition (MPT) pore opening and ROS formation as a mechanism for methamphetamine-induced mitochondrial toxicity. Naunyn Schmiedebergs Arch Pharmacol. 2014;387(1):47–58.

21.

Indo

Davidson

Yen

. Evidence of ROS generation by mitochondria in cells with impaired electron transport chain and mitochondrial DNA damage. Mitochondrion. 2007;7(1-2):106–118.

22.

Turrens

. Superoxide production by the mitochondrial respiratory chain. Biosci Rep. 1997;17(1):3–8.

23.

Wang

Fang

Leonard

Rao

. Cadmium inhibits the electron transfer chain and induces reactive oxygen species. Free Radic Biol Med. 2004;36(11):1434–1443.

24.

Fattal

Budur

Vaughan

Franco

. Review of the literature on major mental disorders in adult patients with mitochondrial diseases. Psychosomatics. 2006;47(1):1–7.

25.

Horn

Barrientos

. Mitochondrial copper metabolism and delivery to cytochrome c oxidase. IUBMB life. 2008;60(7):421–429.

26.

Chen

Druhan

Varadharaj

Chen

Zweier

. Phosphorylation of endothelial nitric-oxide synthase regulates superoxide generation from the enzyme. J Biol Chem. 2008;283(40):27038–27047.

27.

Xue

Liu

Yang

. Chemoprotective effect of N-acetylcysteine (NAC) on cellular oxidative damages and apoptosis induced by nano titanium dioxide under UVA irradiation. Toxicol in Vitro. 2011;25(1):110–116.

28.

Tahara

Navarete

Kowaltowski

. Tissue-, substrate- and site-specific characteristics of mitochondrial reactive oxygen species generation. Free Radic Biol Med. 2009;46(9):1283–1297.

29.

Feng

L.S

Ryan

Frank

. Updates of reactive oxygen species in melanoma etiology and progression. Arch Biochem Biophys. 2014;563:51–55.

30.

Alicia

Kowaltowski, Nadja

. Mitochondria and reactive oxygen species. Free Radic Biol Med. 2009;53(6):885–892.

31.

Andrew

Mayer

. Enzymatic function of nitric oxide synthases. Cardiovasc Res. 1999;43(3):521–531.

32.

Paravicini

Touyz

. NADPH oxidases, reactive oxygen species, and hypertension. Diabetes care. 2008;31(suppl 2):S170–S180.

33.

Landmesser

Dikalov

Price

. Oxidation of tetrahydrobiopterin leads to uncoupling of endothelial cell nitric oxide synthase in hypertension. J Clin Invest. 2003;111(8):1201–1209.

34.

Widder

Guzik

Mueller

. Role of the multidrug resistance protein-1 in hypertension and vascular dysfunction caused by angiotensin II. Arterioscler Thromb Vasc Biol. 2007;27(4):762–768.

35.

Sugiyama

Levy

Michel

. Tetrahydrobiopterin recycling, a key determinant of endothelial nitric-oxide synthase-dependent signaling pathways in cultured vascular endothelial cells. J.Biol Chem. 2009;284(19):12691–12700.

36.

Michel

. No way to relax: the complexities of coupling nitric oxide synthase pathways in the heart. Circulation. 2010;121(4):484–486.

37.

Tiwari

Belenghi

Levine

Oxidative stress increased respiration and generation of reactive oxygen species, resulting in ATP depletion, opening of mitochondrial permeability transition, and programmed cell death. Plant Physiol. 2010;27(8):647–660.

38.

Mootha

Wei

Buttle

. A reversible component of mitochondrial respiratory dysfunction apoptosis can be rescued by exogenous cytochrome c. EMBO J. 2001;20(4):661–671.

39.

Hanson

. Programmed cell death during pollination-induced petal senescence in petunia. Plant Physiol. 2000;122(4):1323–1333.

Evaluation of Mitochondrial Respiratory Chain on the Generation of Reactive Oxygen Species and Cytotoxicity in HaCaT Cells Induced by Nanosized Titanium Dioxide Under UVA Irradiation