Gallic acid induces HeLa cell death via increasing GSH depletion rather than ROS levels

Introduction

Gallic acid (GA; 3,4,5-triphydroxyl-benzoic acid) and its derivatives are broadly distributed in a variety of plants, fruits and foods. Especially, walnuts, green tea, grapes, strawberries, bananas, lemons, pineapples, wines and apple peels are recognized to be high in GA (1). GA is being used as food additives, and preservatives. GA is very well absorbed in humans; free and glucuronidated forms of GA and its main metabolite 4-O-methylgallic have been observed to a large extent in human blood plasma after intake of foods containing plenty of GA (2).

GA possesses various biological or pharmacological activities including anti-bacterial (3), anti-viral (4) and anti-inflammatory effects (5). The major attention given to GA is due to its antitumoral or anticancer effect. For example, GA inhibits the growth of various cancer cells such as lung cancer (6,7), leukemia (8), prostate cancer (9), gastric, colon, breast, cervical and esophageal cancers (10,11). GA can trigger apoptosis via stimulating oxidative stress and/or increasing intracellular Ca2+ levels (6–8,12). However, GA shows somewhat lesser cytotoxicity against normal endothelial and fibroblast cells (13). In addition, GA reveals an anti-apoptotic potential in normal human lymphocytes (14). GA has been considered as a useful phytochemical for cancer chemoprevention (15). Interestingly, GA can be a pro-oxidant or an antioxidant depending on iron or H2O2 in medium and plasma (16,17). Therefore, further studies need to be performed to re-evaluate its biological functions and roles under the different situations.

Reactive oxygen species (ROS) such as superoxide anion (O2•−), hydroxyl radical (•OH) and hydrogen peroxide (H2O2) are involved in many important cellular functions of cell proliferation, differentiation and apoptosis (18,19). Alteration in the redox status of tissues and cells influences the production or metabolism of ROS. They are generated as by-products of mitochondrial respiration or certain oxidases such as nicotinamide adenine dinucleotide phosphate oxidase and xanthine oxidase (20). The primary metabolic antioxidant enzyme is superoxide dismutase (SOD), which metabolize O2•− to H2O2 (21). Further metabolism by other antioxidant enzymes such as catalase and glutathione (GSH) peroxidase, yields O2 and H2O (22). Cells possess various antioxidant systems to control the redox state, which is important for their survival. Oxidative stress may be the result of either overproduction of ROS or accumulation of it due to the failure of antioxidant systems, consequently inducing cell dysfunction or cell death.

Cervical cancer is a foremost cause of cancer-related death in women worldwide. The carcinogenesis is considered to be connected with excessive inflammation mediated by ROS. It was previously demonstrated that GA induces the growth inhibition and death in GA-treated HeLa cervical cancer cells (11). However, the underlying mechanism remains unclear in view of redox state changes in GA-treated HeLa cells. Thus, this study assessed the effects of GA on ROS and GSH levels in HeLa cells and investigated the cellular effects of N-acetyl cysteine (NAC; a well known antioxidant) and buthionine sulfoximine (BSO; an inhibitor of GSH synthesis) on GA-treated HeLa cells in relation to cell death.

Materials and methods

Cell culture

The human cervix adenocarcinoma HeLa cells obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA) were cultured in RPMI-1640 supplemented with 10% fetal bovine serum (Sigma-Aldrich Chemical Co., St. Louis, MO, USA) and 1% penicillin-streptomycin (Gibco BRL, Grand Island, NY, USA). The primary human umbilical vein endothelial cells (HUVEC) purchased from PromoCell GmbH (Heidelberg, Germany) were cultured in complete endothelial cell growth medium (ECGM, Promocell) with 2% FBS. HUVEC were washed and detached with HEPES-BSS (30 mM HEPES), trypsin-EDTA and trypsin neutralization solution (Promocell). The HUVEC between passages four and eight were utilized for the experiments.

Reagents

GA was purchased from the Sigma-Aldrich Chemical Co. and was dissolved in 100% ethanol at 200 mM. NAC and BSO were also obtained from Sigma-Aldrich Chemical Co. NAC and BSO were obtained from Sigma-Aldrich Chemical Co. NAC was dissolved in the buffer [20 mM HEPES (pH 7.0)]. BSO was dissolved in water. Based on a previous study (23), exponentially growing cells were treated with the indicated amounts of GA for 24 or 72 h following one hour pre-incubation of 2 mM NAC or 10 µM BSO.

Growth inhibition assay

Changes in cell growth were assessed by measuring the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT, Sigma-Aldrich Chemical Co.) dye absorbance as previously described (24). Cells were exposed to the indicated amounts of GA with or without NAC or BSO for 24 or 72 h.

Detection of intracellular ROS levels

Intracellular ROS were assessed by a fluorescent probe dye, 2′,7′-dichlorodihydrofluorescein diacetate (H2DCFDA; Invitrogen Molecular Probes, Eugene, OR, USA). Dihydroethidium (DHE, Invitrogen Molecular Probes) is a fluorogenic probe which is highly selective for O2•− among ROS. Cells were incubated with the indicated amounts of GA with or without NAC or BSO for 0.5, 1, 2, 24 or 72 h. Cells were then washed in PBS and incubated with 20 µM H2DCFDA or DHE at 37°C for 30 min. DCF and DHE fluorescences were detected using a FACStar flow cytometer (Becton-Dickinson, Franklin Lakes, NJ, USA). ROS levels were expressed as mean fluorescence intensity (MFI).

Detection of the intracellular glutathione (GSH)

Cellular GSH levels were analyzed using a 5-chloromethylfluorescein diacetate dye (CMFDA, Invitrogen Molecular Probes) as previously described (25). Cells were incubated with the indicated amounts of GA with or without NAC or BSO for 0.5, 1, 2, 24 or 72 h. CMF fluorescence intensity was determined using a FACStar flow cytometer (Becton-Dickinson). Negative CMF staining (GSH depleted) cells were expressed as the percent of (−) CMF cells. CMF levels in cells except (−) CMF cells were expressed as MFI, which was calculated by CellQuest software (Becton-Dickinson).

Annexin V staining for apoptosis detection

Apoptosis was analyzed by staining cells with Annexin V-fluorescein isothiocyanate (FITC; Invitrogen Molecular Probes) as previously described (26). Cells were incubated with the indicated amounts of GA with or without NAC or BSO for 24 h. Annexin V-FITC staining cells were analyzed with a FACStar flow cytometer (Becton-Dickinson).

Measurement of mitochondrial membrane potential (MMP; ∆ψm)

MMP (∆ψm) levels were measured using a Rhodamine 123 fluorescent dye (Sigma-Aldrich Chemical Co.; Ex/Em = 485/535 nm) as previously described (27). Cells were incubated with the indicated amounts of GA with or without NAC or BSO for 24 h. Rhodamine 123 staining intensity was determined by flow cytometry (Becton-Dickinson). An absence of Rhodamine 123 from cells indicated the loss of MMP (∆ψm) in HeLa cells.

Statistical analysis

The data were assessed using Instat software (GraphPad Prism4, San Diego, CA, USA). The Student's t-test or one-way analysis of variance (ANOVA) was used for parametric data. Statistical significance was defined as p<0.05.

Results

Effects of GA on the growth of HeLa cells and HUVEC

The anti-growth effect of GA was examined in HeLa cells and HUVEC using MTT assays. In this study, HUVEC were used as normal control cells since GA shows no cytotoxicity against normal fibroblast and endothelial cells (13). After exposure to GA for 24 h, HeLa cell growth was dose-dependently diminished with an IC50 of ~80 µM GA (Fig. 1A). At 72 h, the growth of HeLa cells was completely inhibited at the concentrations of >100 µM GA (Fig. 1A). When the growth of HUVEC was assessed after treatment with GA, the dose-dependent reduction of cell growth was observed with an IC50 of ~400 µM GA at 24 h (Fig. 1B).

Figure 1. Effects of GA on the growth of HeLa cells and HUVEC in vitro. Exponentially-growing cells were treated with the indicated concentrations of GA for 24 or 72 h. Cell growth inhibition was assessed by MTT assays. (A) HeLa cells at 24 or 72 h. (B) HUVEC at 24 h. *p<0.05 as compared with the GA-untreated control group.

Effects of GA on intracellular ROS levels in HeLa cells and HUVEC

To assess ROS levels in GA-treated HeLa cells and HUVEC, H2DCFDA and DHE dyes were used for the detection of non-specific ROS and O2•− levels, respectively. As shown in Fig. 2A and B, intracellular ROS (DCF) levels increased in HeLa cells treated with 50–400 µM GA from the early time phase of 30 min to 24 h. ROS levels dose-dependently increased at 24 h (Fig. 2A and B). However, 50 or 100 µM GA decreased ROS levels in HeLa cells at 72 h (Fig. 2B). In HUVEC, 100 or 200 µM GA increased ROS levels at 24 h whereas 400 and 800 µM GA did not affect ROS levels at this time (Fig. 2C).

Figure 2. Effects of GA on ROS levels in HeLa cells and HUVEC. Exponentially-growing cells were treated with the indicated concentrations of GA for 0.5, 1, 2, 24 or 72 h. (A) Each histogram shows the levels of ROS (DCF) in GA-treated HeLa cells at 24 h. (B and C) Graphs indicate DCF (ROS) levels (%) in HeLa cells (B) and HUVEC (C) as compared with each control group cells. (D) Each histogram shows the levels of O2•− (DHE) in GA-treated HeLa cells at 24 h. (E and F) Graphs indicate DHE (O2•−) levels (%) in HeLa cells (E) and HUVEC (F) as compared with each control group cells. *p<0.05 as compared with the GA-untreated control group.

Intracellular O2•− levels slightly decreased in 200 or 400 µM GA-treated HeLa cells from 1 h to 2 h whereas O2•− levels were not significantly changed in 50 or 100 µM GA-treated HeLa cells during these times (Fig. 2E). At 24 h, O2•− levels dose-dependently increased in GA-treated HeLa cells (Fig. 2D and E). The O2•− levels increased by 50 or 100 µM GA lasted for 72 h (Fig. 2E). In addition, 200–800 µM GA increased O2•− levels in HUVEC at 24 h (Fig. 2F).

Effects of GA on intracellular GSH levels in HeLa cells and HUVEC

Next, changes in GSH levels were analyzed in GA-treated HeLa cells and HUVEC using CMF fluorescence dye. As shown in Fig. 3A and B, the numbers of GSH-depleted cells in GA-treated HeLa cells were dose-dependently increased at 24 or 72 h. A dramatic increase in GSH-depleted cell number was observed in above 100 µM GA-treated cells at 24 or 72 h (Fig. 3A and B). However, the tested doses of GA did not induce GSH depletion in HeLa cells at 1 h (Fig. 3B). In HUVEC, 100 or 200 µM GA did not increase the numbers of GSH-depleted cells at 24 h, but 400 or 800 µM GA strongly increased the numbers (Fig. 3C). When GSH levels were measured in GA-treated HeLa cells at the early time phases of 0.5, 1 or 2 h, GSH levels seemed to be decreased by GA during these times (Fig. 3D).

Figure 3. Effects of GA on GSH levels in HeLa cells and HUVEC. Exponentially-growing cells were treated with the indicated concentrations of GA for 0.5, 1, 2, 24 or 72 h. (A) Each histogram shows the levels of GSH (CMF) in HeLa cells at 24 or 72 h. M1 indicates the region of GSH depleted cells. (B) Graph shows the percents of (−) CMF (GSH-depleted; M1 region) cells in HeLa cells at 1, 24 or 72 h. (C) Graph shows the percents of (−) CMF (GSH-depleted) cells in HUVEC at 24 h. (D) Graph indicates mean CMF (GSH) levels (%) in HeLa cells at 0.1, 1 or 2 h as compared with each control group cell. *p<0.05 as compared with the GA-untreated control cell group.

Effects of NAC and BSO on cell death and MMP (∆ψm) in GA-treated HeLa cells

Because GA inhibited the growth of HeLa cells, this study investigated the effects of NAC or BSO on the growth and death of 50 or 100 µM GA-treated HeLa cells at 24 h. Treatment with NAC significantly decreased the growth of 50 µM GA-treated HeLa cells and BSO slightly decreased the growth (Fig. 4A). In addition, 50 µM GA slightly increased the numbers of Annexin V-FITC-positive cells in HeLa cells, but 100 µM GA strongly increased Annexin V-FITC-positive cell numbers (Fig. 4B). NAC, but not BSO, increased the numbers of Annexin V-FITC-positive cells in 50 µM GA-treated HeLa cells (Fig. 4B). Furthermore, mitochondrial membrane potential (MMP; ∆ψm) levels in GA-treated HeLa cells were analyzed in the presence or absence of NAC and BSO at 24 h. Similar to the Annexin V staining results, 100 µM, but not 50 GA µM, markedly triggered the loss of MMP (∆ψm) in HeLa cells (Fig. 4C). Both NAC and BSO significantly increased the loss of MMP (∆ψm) in 50 µM GA-treated HeLa cells (Fig. 4C). NAC or BSO alone did not trigger the loss of MMP (∆ψm) in HeLa control cells (data not shown).

Figure 4. Effects of NAC and BSO on cell growth, death and MMP (∆ψm) in GA-treated HeLa cells. Exponentially-growing HeLa cells were treated with 50 or 100 µM GA for 24 h following 1 h pre-incubation of 2 mM NAC or 10 µM BSO. (A) Graph shows the growth of HeLa cells, as assessed by an MTT assay. (B and C) Graphs show the percents of Annexin V-FITC staining cells (B) and Rhodamine 123-negative [MMP (∆ψm) loss] cells (C), as measured with a FACStar flow cytometer. *p<0.05 as compared with the control group. #p<0.05 as compared with cells treated with 50 µM GA only.

Effects of NAC and BSO on ROS and GSH levels in GA-treated HeLa cells

It was assessed whether ROS and GSH levels in GA-treated HeLa cells were changed or not by NAC or BSO at 24 h. As shown in Fig. 5A, ROS (DCF) level in 50 µM GA-treated HeLa cells was significantly decreased by NAC whereas BSO strongly increased ROS (DCF) level in these cells. NAC and BSO did not alter ROS (DCF) level in 100 µM GA-treated HeLa cells (Fig. 5A). In contrast, NAC intensified O2•− level in 50 µM GA-treated HeLa cells and slightly increased O2•− level in 100 µM GA-treated HeLa cells (Fig. 5B). BSO slightly decreased O2•− level in 50 µM GA-treated HeLa cells but it increased O2•− level in 100 µM GA-treated HeLa cells (Fig. 5B). In relation to GSH level, NAC and BSO significantly increased the numbers of GSH-depleted cells in 50 µM GA-treated HeLa cells at 24 h (Fig. 5C). Both agents also mildly increased GSH-depleted cell numbers in 100 µM GA-treated HeLa cells (Fig. 5C). NAC or BSO alone did not significantly change GSH and ROS levels including O2•−.

Figure 5. Effects of NAC and BSO on ROS and GSH levels in GA-treated HeLa cells. Exponentially-growing HeLa cells were treated with 50 or 100 µM GA for 24 h following 1 h pre-incubation of 2 mM NAC or 10 µM BSO. (A and B) Graphs indicate DCF (ROS) and DHE (O2•−) levels (%) as compared with control HeLa cells, respectively. (C) Graph shows the percents of (−) CMF (GSH-depleted) cells. *p<0.05 as compared with the control group. #p<0.05 as compared with cells treated with 50 µM GA only.

Discussion

This study focused on evaluating the effects of GA on the growth and death of HeLa cells in relation to ROS and GSH levels. This study also demonstrated that the susceptibility of HeLa cells to GA was higher than that of HUVEC. This result was similar to the report that GA shows the lower cytotoxicity against normal fibroblast and endothelial cells (13). GA is reported to induce apoptosis in prostate cancer cells via mitochondrial dysfunction (28). Likewise, GA seemed to induce apoptosis in HeLa cells and it triggered the loss of MMP (∆ψm).

GA has been reported to have both pro-oxidant and/or antioxidant properties (16,17). Increasing evidence suggests that apoptosis induced by GA is associated with oxidative stresses derived from ROS (8,12,28). According to our results, the intracellular ROS (DCF) levels increased in GA-treated HeLa cells from the early time phases. ROS levels also dose-dependently increased at 24 h. Interestingly, 50 or 100 µM GA showing an apoptotic effect at 72 h decreased ROS levels. In contrast, GA slightly decreased O2•− levels at the early time phases and it increased O2•− levels at 24 or 72 h. In relation to HUVEC, 100 or 200 µM GA increased ROS levels at 24 h whereas 400 and 800 µM GA showed a significant growth inhibition and cell death did not increase ROS levels. Treatment with the >200 µM GA increased O2•− levels in HUVEC at 24 h. In addition, GA increases ROS levels including O2•− at 24 h in lung cancer and normal cells (7,29). These results suggest that GA can individually affect different ROS levels depending on the incubation times and doses, and cell types.

NAC showing the reduction of ROS (DCF) level in 50 µM GA-treated HeLa cells significantly enhanced growth inhibition and cell death in these cells. In addition, NAC strongly increased O2•− level in GA-treated HeLa cells. Therefore, although NAC decreased ROS (DCF) level in GA-treated HeLa cells, NAC seemed to act as a pro-oxidant because of increasing O2•− level and cell death in these cells. Similarly, NAC intensified the growth inhibition and death in GA-treated lung cancer, which were accompanied by a decrease in ROS (DCF) level and an increase in O2•− level (7). BSO showing a strong increased effect of ROS (DCF) on GA-treated HeLa cells did not affect cell growth and death but it increased the loss of MMP (∆ψm) in these cells. Taken together, these results suggest that changes in ROS levels by GA are not tightly but at least partially related to HeLa cell death. The exact role of ROS, especially O2•− needs to be defined further in GA-induced HeLa cell death.

It has been reported that the intracellular GSH content has a decisive effect on anticancer drug-induced apoptosis, indicating that apoptotic effects are inversely comparative to GSH content (30,31). The intracellular GSH content also is involved in GA-induced cell death (7,29). Likewise, GA dose-dependently increased the numbers of GSH-depleted cells in HeLa cells and HUVEC. The decreased GSH levels in GA-treated HeLa cells at the early times probably resulted from ROS (DCF) level increased by GA. In addition, NAC showing the enhancement of cell death in GA-treated HeLa cells significantly increased the numbers of GSH-depleted cells. Similarly, NAC enhances GSH depletion in GA-treated lung cancer and normal cells (7,29). Although it is known that NAC as a GSH precursor contains a thiol group, NAC used in this study did not seem to be a GSH precursor in GA-treated HeLa cells. However, NAC significantly prevented GSH depletion in propyl gallate-treated HeLa cells (32). Therefore, it is considered that NAC can be a GSH precursor or not depending on co-incubated agents. BSO significantly increased the numbers of GSH-depleted cells in GA-treated HeLa cells. BSO also augmented GSH depletion and cell death in GA-treated lung cancer and normal cells (7,29). However, BSO enhanced the loss of MMP (∆ψm) in GA-treated HeLa cells without a significant increase in cell death, implying that GSH depletion in these cells was correlated with MMP (∆ψm) loss rather than cell death. Taken together, these results suggest that the intracellular GSH content seem to have a vital role on GA-induced cell death but changes in GSH levels are not sufficient enough to precisely predict cell death.

In conclusion, GA significantly inhibited the growth of HeLa cells. Changes in ROS levels, especially O2•− affected GA-induced HeLa cell death. GA-induced HeLa cell death correlated with GSH depletion.

Acknowledgements

This study was supported by a grant from the National Research Foundation of Korea (NRF) funded by the Korean government (MSIP; nos. 2008-0062279 and 2016R1A2B4007773).

Glossary

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References