Introduction
Periodontitis is a chronic inflammatory disease, which is characterized by bleeding, destruction of connective tissues and alveolar bone loss (1–3). In addition, periodontitis is reported to be implicated in the onset of a variety of diseases, including diabetes, rheumatoid arthritis and cardiovascular disease (4). The occurrence of periodontitis is ascribed to multiple factors. Of these, with the exception of bacterial infection and host contributing factors, the role of oxidative stress in the development and pathogenesis of periodontitis has been elucidated (5). Therefore, detailed investigation of the association between oxidative stress and periodontitis is of crucial importance.
Reactive oxygen species (ROS), which markedly contribute to cellular oxidative stress, are important signaling mediators in several biological processes (6). Living organisms have adapted to the efflux of ROS, in which antioxidants, including vitamin C (Vc) are important in counteracting the oxidative effects (7). These reactive species are generated from molecular oxygen and, if they are not cleared by the antioxidative system, these highly reactive species induce significant damage in the cellular environment (2). An imbalance between the upregulation of pro-oxidants and antioxidants can lead to severe impairment of critical cellular structures, membrane dysfunction and cell death by necrosis or apoptosis (8). Subtle alterations in the intracellular redox state initiates cellular events associated with altered gene expression and may eventually lead to destruction of or damage to the tooth supporting tissues secondary to the induction of proinflammatory processes.
The periodontal ligament (PDL) is an assembly of specialized tooth supporting tissue fibers that attach root cement to alveolar bone (9). The PDL is composed of diverse cell subpopulations, including fibroblasts and osteoblasts, with PDL cells (PDLCs) constituting the majority. PDLCs have fibroblast-like features and are able to produce collagen whilst simultaneously retaining osteoblastic features (10). The secreted collagens build up the PDL to ensure the attachment of root cement to alveolar bone and tissue recovery following injury. Human PDLCs also produce cytokines and chemokines in conditions of stress, which are characteristic of leucocytes and macrophages (9). In addition, the abnormal reduction or structural destruction of PDLCs increase the likelihood of pathogenesis in the periodontal tissues implying that PDLCs may be important in initiating periodontal inflammation.
Given the proinflammatory status of periodontal tissues, ROS can also be linked to the pathogenesis of periodontitis. Hydrogen peroxide (H2O2) is a type of ROS, which is generated by almost all types of oxidative stress and infiltrates cells through their membrane. H2O2 has a broad spectrum of biological effects, while the cellular responses to H2O2 may differ in a cell type and concentration-specific manner (11,12). H2O2 may induce growth inhibitory effects, whereas in a similar setting it may also promote proliferation in other cell types (13). In addition a dual association between apoptosis and the concentration of H2O2 has been demonstrated, which further complicates the exact functionality of H2O2 exposure to cellular events (14).
Materials and methods
Cell culture
The study was approved by the Ethics Committee of the Institute and Hospital of Stomatology, Nanjing University Medical School (Nanjing, China). Primary human PDLCs were obtained from premolars, which were extracted from healthy patients aged between 10 and 18 years with no evidence of gingivitis, periodontitis or caries. All patients provided informed consent prior to sample collection. In brief, the human PDL tissues were obtained from the central tooth root surface using a surgical scalpel. The obtained tissues were then cultured in Dulbecco’s modified Eagle’s medium supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin solution (50 g/ml streptomycin and 5,000 U/ml penicillin; Sigma Aldrich, St. Louis, MO, USA) at 37°C and 5% CO2 in a humidified atmosphere. The medium was replaced every 2–3 days. When the cultured PDLCs reached confluence, they were trypsinized and divided at a ratio of 1:2 with 0.25% trypsin solution (Sigma Aldrich). Cells at passages 4–5 were used in the present study.
MTT assay
The PDLCs were seeded into a 96-well-plate overnight at 37°C and were then washed with phosphate-buffered saline (PBS; Kangchen Biotech, Shanghai, China). The cells were treated with different concentrations of H2O2 (600, 800 or 1,000 μM) for the indicated time periods between 0 and 48 h. MTT solution (20 μl; 5 mg/ml; Kangchen Biotech) was then added to each well. After 4 h incubation at 37°C, the media was removed and 100 μl dimethyl sulfoxide (Kangchen Biotech) was added to each well in the plate to dissolve the purple formazan crystals. The plate was then agitated for 10 min for solubilization and the spectrophotometric absorbance at 540 nm was calculated using a Multilabel Counter (Safire; Tecan Austria GmbH, Grödig, Austria).
Flow cytometry
The cells were collected at specific time points (3 or 6 h) following H2O2 treatment, washed in PBS and fixed using 75% ethanol overnight at −20°C. The fixed PDLCs were then washed with cold PBS and stained using 5 μl annexin V-fluorescein isothiocyanate (Kangchen Biotech) and propidium iodide (PI) solutions (0.1% Triton X-100, 100 mg/ml PI and 0.01 mg/ml RNase; Kangchen Biotech) for 30 min at 4°C in the dark. The successfully stained PDLCs were further analyzed using a FACScan laser flow cytometer (Becton-Dickinson, Franklin Lakes, NJ, USA).
Western blot analysis
The PDLCs were incubated following treatment with various concentrations of H2O2 and Vc for either 3 or 6 h. Following incubation, the PDLCs were harvested and lysed. The proteins were then quantified using a bicinchoninic acid protein assay kit (Pierce Biotechnology, Inc., Rockford, IL, USA) according to the manufacturer’s instructions. The proteins were electrophoresed on a 12% SDS-PAGE gel for western blot analysis, followed by immunoblotting on a polyvinylidene difluoride membrane (Amersham Biosciences, Pittsburgh, PA, USA). Caspase-3 antibodies were purchased from Bioworld Technology, Inc. (St. Louis Park, MN, USA; cat no. BS1518). Mouse monoclonal antibodies for caspase-9 and PARP were obtained from Cell Signaling Technology, Inc. (Danvers, MA, USA; cat nos. 9508 and 9532, respectively). The proteins were incubated with the antibodies overnight at 4°C and subsequently with peroxidase-labeled anti-rabbit or anti-mouse antibodies (Kangchen Biotech) for 1 h at room temperature. Quantification of the blots was performed using a chemiluminescent method kit from Sino-American Biotechnology (Henan, China).
Statistical analysis
Statistical comparisons were performed using Welch’s t-test or analysis of variance followed by Dunnett’s test. P<0.05, P<0.01 and P<0.001 were considered to indicate statistically significant differences.
Results
Identifying the optimal H<sub>2</sub>O<sub>2</sub> concentration for decreased PDLC viability
ROS have been suggested to induce marked destruction in periodontal tissues. To identify whether H2O2 exerts a toxic effect on PDLCs and to determine which concentration of H2O2 causes a significant decrease in PDLC viability, the PDLCs were treated with different concentrations of H2O2 for the indicated time periods (Fig. 1). The results demonstrated a significant decrease in PDLC viability 3 h post-H2O2 treatment at concentrations >600 μM (Fig. 1A). At 600 μM H2O2, ~50% of the PDLCs were lost and the toxic effects of H2O2 were relatively stable at higher levels of H2O2 (Fig. 1A). Extending the treatment time to 6 h led to similar results (Fig. 1B) demonstrating that >600 μM H2O2 caused PDLC death within at least 6 h. Therefore, H2O2 concentrations of 600, 800 and 1,000 μM were selected for further investigation.
High levels of H<sub>2</sub>O<sub>2</sub> result in morphological alterations and apoptosis in PDLCs
To evaluate the cytotoxic effect of H2O2 on cell morphology, the PDLCs were treated with different concentrations of H2O2 (600–1,000 μM) for 3 or 6 h. Subsequently, morphological alterations in the PDLCs were monitored. The untreated cells remained intact (Fig. 2A), however, when the PDLCs were treated with high levels of H2O2 (800 and 1,000 μM), the basic structure of the cells was lost, particularly at 1,000 μM H2O2 (Fig. 2A). The cytotoxic effects on morphology were more evident 6 h post-stimulation (Fig. 2B) and the proportion of cells exhibiting shrinkage and loss of intact structure generally increased with increased H2O2 levels (Fig. 2A and B). Taken together, these results suggested that H2O2 induced PDLC death through apoptosis in a dose- and time-dependent manner.
Optimal concentrations of Vc antagonizes H<sub>2</sub>O<sub>2</sub>-induced cell death
Several studies have suggested that the high degree of free radicals generated by bacterial stimulation function as an integrated part of host defense to infection and result in marked oxidative damage of periodontal tissues (2,3,11). The damage mediated by free radicals can be mitigated by the antioxidant defense system. To gain further insights into the potential protective effect of antioxidants, PDLCs were treated with different concentrations of Vc and the viability of cells was evaluated (Fig. 3). Relatively high levels of Vc (50–200 μM) were found to be cytotoxic, even without additional H2O2 treatment, with the exception of 10 μM Vc (Fig. 3). These results suggested that Vc exerted pro-survival effects on H2O2-treated cells at specific concentrations only.
Optimal Vc antagonizes the adverse effect of H<sub>2</sub>O<sub>2</sub>
To understand the role of Vc, PDLCs were treated with different concentrations of Vc together with 800 or 1,000 μM H2O2. The viability of the PDLCs was monitored at 3 and 6 h. PDLCs did not retain their intact structure when treated with H2O2 for 3 or 6 h (Fig. 4A and B). However, Vc administration partially reversed the adverse effect of H2O2 treatment and this effect was more marked when the cells were treated with 1,000 μM H2O2 (Fig. 4A and B). The antioxidative effect of Vc was also evaluated using an MTT assay. The results demonstrated a clear cytoprotective effect of Vc even at <600 μM H2O2 for 3 h. (Fig. 4C). This antioxidative effect was even more clear when the PDLCs were treated with 1,000 μM H2O2 (Fig. 4C). The viability of challenged PDLCs was increased at all H2O2 concentrations 3 and 6 h post stimulation (Fig. 4C). These results suggested that optimal Vc administration increased the viability of PDLCs under oxidative stress and exerted a cytoprotective effect.
Optimal Vc rescues PDLCs under oxidative stress by decreasing apoptosis
The results of the present study demonstrated that treatment of PDLCs with >10μM Vc consistently exhibited a robust cytoprotective effect. Subsequent investigation was performed using flow cytometry to determine whether Vc had a potential anti-apoptotic function. The results demonstrated that 1,000 μM H2O2 was capable of initiating apoptosis in the PDLCs, while Vc protected the PDLCs from H2O2 exposure at 3 h post stimulation (Fig. 5A). In the cells treated with lower concentrations of H2O2 (600 and 800 μM), apoptosis was not attenuated by the addition of Vc at 3 h, possibly due to the limited time scale (Fig. 5A). Similar results were observed when the apoptotic effects were evaluated at 6 h (Fig. 5B). The apoptosis observed following H2O2 exposure at 800 and 1,000 μM was also verified by the occurrence of cleaved caspase-3, caspase-9 and PARP using western blot analysis (Fig. 6). However, following the addition of 10 μM Vc, the level of cleaved caspases-3, caspases-9 and PARP all decreased implying impairment of the apoptotic response (Fig. 6). These results suggested that optimal Vc administration antagonized the oxidative effect of H2O2 and effectively improved the survival of PDLCs at high levels of H2O2, even at earlier time points.
Discussion
Oxidative stress is central to periodontal tissue damage and periodontitis, either due to excess ROS production/activity, antioxidant deficiency or indirectly as a result of activating specific transcription factors that lead to a pro-inflammatory state. A significant association between abnormal oxidative status and periodontal diseases has been demonstrated implying that oxidative stress may be a determinant in the progression of periodontitis (13). Therefore, detailed investigation of the oxidative status in periodontal tissues may provide crucial insights into the pathological and pharmaceutical intervention of periodontitis. In the present study, the role of H2O2 was examined and H2O2 was found to induce the apoptosis of PDLCs in a dose- and time-dependent manner (Figs. 2 and 3). Furthermore, Vc supplementation partially reversed the adverse effect of H2O2 (Figs. 4, 5 and 6), however, the addition of Vc did not always improve survival of the PDLCs, supporting the existence of an optimal level of Vc to decrease PDLC death (Fig. 3).
Several studies have associated oxidative stress with the pathogenesis of periodontitis (15–17). For example, high levels of ROS in the gingivae and saliva are associated with the progression of periodontal diseases (14). In addition, excess ROS and a marked reduction in antioxidant levels in gingival crevicular fluid are responsible for chronic periodontitis (14,16). The local assembly of pro-inflammatory lymphocytes and the release of ROS are major triggers of host defense for those suffering from periodontitis (18). Evidence from animal studies has also demonstrated a significant association between higher levels of ROS and periodontitis (14). Despite these findings, to the best of our knowledge, no studies have established a role of ROS levels in PDLCs or investigated the mechanisms by which ROS may affect the viability of PDLCs. The present study demonstrated that H2O2 may decrease the viability of PDLCs by inducing programed cell death in a dose- and time-dependent manner. This apoptosis was verified using flow cytometric analysis and the occurrence of cleaved caspase-3, caspase-9 and PARP (Fig. 6). These observations suggest that at least the mitochondrial apoptotic pathway may be involved in eliminating PDLCs exposed to H2O2. This mechanistic investigation provides insights into how increased ROS levels may lead to periodontal tissue destruction and supports the hypothesis that ROS excess further exacerbates periodontal tissue damage by inducing the apoptosis of PDLCs. These findings also demonstrated the importance of ROS control in periodontitis. Therefore, administration of antioxidants may be favorable in the treatment of periodontitis, which prompted the present study to investigate the pharmacological effects of Vc exposure.
Few studies, to the best of our knowledge, have examined the role of the antioxidative effect of Vc in PDLCs. Therefore, the current study investigated how oxidative status affected the viability of PDLCs and whether stressed cells can be recovered by administration of the antioxidant Vc. Notably, Vc was found to rescue H2O2-challenged PDLCs in a dose-dependent manner. However, the viability of H2O2-challenged PDLCs did not monotonically increase with increasing Vc concentration. These results suggested that there may be an optimal Vc concentration for the maximal survival of PDLCs in conditions of H2O2 stress. Vc is able to either promote or inhibit apoptosis in a dose and cell type-specific manner (19–24). For example, Vc exacerbated rather than inhibited H2O2-induced apoptosis in epithelial and mesenchymal cells(19). Additionally, Vc alone has also been observed to exhibit cell type-specific effects in the regulation of apoptosis (19) and has a cytotoxic effect on the human gastric cancer cell line AGS, possibly by downregulating 14–3–3σ proteins (20). In human breast cancer cells, Vc acts through apoptosis inducing factor to initiate apoptosis (24). Therefore, the interpretation of Vc-induced cytotoxic effects may be complex and may depend on cell milieus, dose used and the availability of other cofactors. A dose-dependent effect of Vc addition has been demonstrated in L6 muscle cells, where micromolar quantities of Vc increased apoptosis but millimolar doses were notably protective (25). Therefore, the clinical use of antioxidants, particularly Vc, requires cautious administration, as the addition of Vc may be cytotoxic under certain conditions. In the present study, it was clear that optimal use of Vc lowered the risk of cellular apoptosis at as early as 3 h post stimulation (Figs. 4 and 5) and this observation provides a deeper understanding of clinical intervention for the treatment of periodontitis.
Several experimental limitations in the present study must be noted. Although the mitochondrial apoptotic pathway was found to be involved in inducing the apoptosis of PDLCs, the importance of other apoptotic pathways requires further investigation. In addition, whether PDLCs are subject to other programs of cell death may be examined in future studies. The mechanism underlying the decreased survival of PDLCs by excess Vc also requires investigation. Although the present study did not enable the inference of a causal association between H2O2 exposure and the development of periodontitis, the importance of optimal Vc administration was evident, even without prior knowledge of the exact association.
In conclusion, the present study demonstrated that H2O2 disrupted the morphology and decreased the viability of PDLCs via apoptotic pathways. In addition, the optimal dose of Vc in treating periodontitis was revealed to be important, as excess Vc usage may otherwise induce cell death and exacerbate the progression of periodontitis. These results also clarified evidence that ROS exert toxic effects on PDLCs. These findings may broaden current knowledge of the pathogenesis of periodontitis and may have significant implications for therapeutic intervention.