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Sargassum horneri methanol extract rescues C2C12 murine skeletal muscle cells from oxidative stress-induced cytotoxicity through Nrf2-mediated upregulation of heme oxygenase-1
- Ji Sook Kang†1,
- Il-Whan Choi†2,
- Min Ho Han3,
- Su Hyun Hong4,
- Sung Ok Kim5,
- Gi-Young Kim6,
- Hye Jin Hwang1, 3, 7,
- Byung Woo Kim1, 3, 8,
- Byung Tae Choi9,
- Cheol Min Kim10 and
- Yung Hyun Choi1, 3, 4Email author
© Kang et al.; licensee BioMed Central. 2015
Received: 13 September 2014
Accepted: 20 January 2015
Published: 5 February 2015
Sargassum horneri, an edible marine brown alga, is typically distributed along the coastal seas of Korea and Japan. Although several studies have demonstrated the anti-oxidative activity of this alga, the regulatory mechanisms have not yet been defined. The aim of the present study was to examine the cytoprotective effects of S. horneri against oxidative stress-induced cell damage in C2C12 myoblasts.
We demonstrated the anti-oxidative effects of a methanol extract of S. horneri (SHME) in a hydrogen peroxide (H2O2)-stimulated C2C12 myoblast model. Cytotoxicity was determined using the 3-(4,5-dimetylthiazol-2-yl)-2,5-diphenyl-tetrazolium assay and mode of cell death by cell cycle analysis. DNA damage was measured using a comet assay and expression of phospho-histone γH2A.X (p-γH2A.X). Levels of cellular oxidative stress as reactive oxygen species (ROS) accumulation were measured using 2’,7’-dichlorofluorescein diacetate. The involvement of selected genes in the oxidative stress-mediated signaling pathway was explored using Western blot analysis.
SHME attenuated H2O2-induced growth inhibition and exhibited scavenging activity against intracellular ROS that were induced by H2O2. The SHME also inhibited comet tail formation, p-γH2A.X expression, and the number of sub-G1 hypodiploid cells, suggesting that it prevents H2O2-induced cellular DNA damage and apoptotic cell death. Furthermore, the SHME significantly enhanced the expression of heme oxygenase-1 (HO-1) associated with induction of nuclear factor-erythroid 2 related factor 2 (Nrf2) in a time- and concentration-dependent manner. Moreover, the protective effect of the SHME on H2O2-induced C2C12 cell damage was significantly abolished by zinc protoporphyrin IX, a HO-1 competitive inhibitor, in C2C12 cells.
These findings suggest that the SHME augments cellular antioxidant defense capacity through both intrinsic free radical scavenging activity and activation of the Nrf2/HO-1 pathway, protecting C2C12 cells from H2O2-induced oxidative cytotoxicity.
Oxidative stress is defined as a disturbance in the balance between the production of reactive oxygen species (ROS) and antioxidant defenses. ROS are ions or small molecules including oxygen species, that are produced as normal products of cellular metabolism. Substantial data have shown the essential role of oxidative stress in the regulation of diverse cellular events [1,2]. Furthermore, some ROS act as cellular messengers during redox signaling. However, disturbances in the normal redox state of cells and/or a concomitant decline in antioxidant scavenging capacity can cause toxic effects through the production of peroxides and free radicals that damage all components of the cell, including proteins, lipids, and nucleic acids. Moreover, elevated production of ROS increases oxidative stress, leading to cellular dysfunction and, eventually, apoptotic cell death [3-5]. Thus, oxidative stress can cause disruptions in normal cellular signaling mechanisms.
Because ROS formation occurs naturally, mammalian cells have developed several adaptive mechanisms to limit ROS formation or to detoxify ROS. These mechanisms use antioxidant enzymes or antioxidant compounds. Among the various antioxidant enzymes, the protective role of heme oxygenase-1 (HO-1), an inducible isoform of the first and rate-limiting enzyme of heme degradation, against oxidative stress, has been emphasized [6-8]. HO-1 is regulated by the nuclear factor-erythroid 2-related factor 2 (Nrf2)-antioxidant response element (ARE) pathway, and induction of this enzyme protects cells against oxidative stress-induced cell death and tissue injury. Antioxidants are essential substances that possess the ability to protect cells from damage caused by ROS-mediated oxidative stress [9-11]. For this reason, many investigators have searched for natural antioxidants that have safe and effective pharmacological activity with low cytotoxicity and that prevent oxidative stress-mediated cellular damage.
Seaweeds have been rich sources of minerals, vitamins, and dietary fiber in East Asia for centuries [12,13]. Today, they are highlighted as multifunctional foods for maintaining health. Among them, Sargassum horneri (Turner) C. Agardh, an edible brown alga, is usually found in the coastal seas of Korea and Japan. Generally, S. horneri demonstrates antivirus [14-16], antioxidant [17,18], and anticoagulant activities , and preventative effects on bone loss by stimulating osteoblastic bone formation . The protective actions of S. horneri against ultra violet (UV) A-induced damage have been reported; in particular, the chromene compound isolated from S. horneri shields human dermal fibroblasts from UV A-induced oxidative stress [21,22]. However, little research has been reported regarding the protective effects of S. horneri against oxidative stress. Thus, the aim of this study was to examine the ability of a S. horneri methanol extract (SHME) to protect C2C12 murine skeletal muscle cells from hydrogen peroxide (H2O2)-induced cell damage and to determine the mechanism underlying these protective effects.
Preparation of the SHME
The SHME (stock number AC023) was purchased from Jeju Bio-Resource Extract Bank (Jeju HI-Tech Industry Development Institute, Jeju, Republic of Korea). Briefly, fresh S. horneri, which was authenticated by Professor S.H. Hong, Department of Biochemistry, Dongeui University College of Oriental Medicine (Busan, Republic of Korea), collected along the Jeju Island coast of Korea in July 2005, was washed three times with tap water to remove salt, epiphytes, and sand before storage at -20°C. The frozen samples were lyophilized and homogenized using a grinder before extraction. The dried powder was extracted with 70% methanol (SHME) and evaporated in vacuo and dissolved in dimethyl sulfoxide (DMSO, Sigma-Aldrich Chemical Co., St. Paul, MN, USA). A voucher specimen (accession number DEU-25) was deposited at the Natural Resource Bank of Dongeui University College of Oriental Medicine.
Cell culture and treatment
Mouse-derived C2C12 myoblasts obtained from the American Type Culture Collection (Manassas, VA, USA) were cultured in Dulbecco’s modified Eagle’s medium (DMEM, Gibco-BRL, Gaithersburg, MD, USA) supplemented with 10% heat-inactivated fetal bovine serum (FBS, Gibco-BRL), 100 U/ml penicillin G, 100 μg/ml streptomycin, and 0.25 μg/ml amphotericin fungizone at 37°C in a humidified atmosphere of 5% CO2 in air. The SHME was dissolved in DMSO as a stock solution at 50 mg/ml, and the stock solution was then diluted with medium to the desired concentration prior to use.
Cell viability assay
C2C12 cells were seeded in 6-well plates at a density of 1 × 105 cells per well. After a 24-h incubation, the cells were treated with various concentrations of SHME in the absence or presence of H2O2 and/or zinc protoporphyrin IX (ZnPP, Sigma-Aldrich) for the times indicated. An MTT (3-(4,5-dimetylthiazol-2-yl)-2,5-diphenyl-tetrazolium, Sigma-Aldrich) working solution was added to the culture plates and incubated for 3 h at 37°C. The culture supernatant was removed from the wells, and DMSO was added to completely dissolve the formazan crystals. The absorbance of each well was measured at 540 nm with a microplate reader (Molecular Devices, Palo Alto, CA, USA). The effect of the SHME on cell growth was assessed as the percentage of cell viability, where the vehicle-treated cells were considered 100% viable.
Morphological changes were monitored by obtaining photomicrographs under an inverted phase contrast microscope (Carl Zeiss, Oberkochen, Germany).
Comet assay (single-cell gel electrophoresis)
The cell suspension was mixed with 0.5% low melting agarose (LMA) at 37°C, and the mixture was spread on a fully frosted microscopic slides precoated with 1% normal melting agarose. After solidification of the agarose, the slide was covered with 0.5% LMA and then immersed in a lysis solution (2.5 M NaCl, 100 mM Na-EDTA, 10 mM Tris, 1% Triton X-100, and 10% DMSO, pH 10) for 1 h at 4°C. The slides were then placed in a gel electrophoresis apparatus containing 300 mM NaOH and 10 mM Na-EDTA (pH 13) for 40 min to allow for DNA unwinding and expression of alkali-labile damage, and then an electrical field was applied (300 mA, 25 V) for 20 min at 4°C to draw the negatively charged DNA toward the anode. After electrophoresis, the slides were washed three times for 5 min at 4°C in a neutralizing buffer (0.4 M Tris, pH 7.5), followed by staining with 20 μg/ml propidium iodide (PI, Sigma-Aldrich). The slides were examined under a fluorescence microscope (Carl Zeiss).
Protein extraction and Western blot analysis
After removing the media, the cells were washed with ice-cold PBS and gently lysed for 20 min in ice-cold lysis buffer (40 mM Tris, pH 8.0, 120 mM, NaCl, 0.5% NP-40, 0.1 mM sodium orthovanadate, 2 μg/ml leupeptin, and 100 μg/ml phenymethylsulfonyl fluoride). The supernatants were collected and protein concentrations were determined using a Bio-Rad protein assay kit (Bio-Rad, Hercules, CA, USA). For Western blotting, equal amounts of protein extracts (typically 30 μg) were separated by denaturing SDS-polyacrylamide gel electrophoresis and transferred electrophoretically to PVDF membranes (Schleicher & Schuell, Keene, NH, USA). The membranes were incubated overnight at 4°C with primary antibodies, probed with enzyme-linked secondary antibodies (Amersham, Arlington Heights, IL, USA) for 1 h at room temperature, and detected using an enhanced chemiluminescence (ECL) detection system (Amersham). Antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and Cell Signaling Technology (Danvers, MA, USA).
Measurement of ROS
The cells were incubated with 10 μM 2’,7’-dichlorofluorescein diacetate (DCF-DA, Molecular Probes, Eugene, OR, USA) for 20 min at room temperature in the dark to monitor ROS production. ROS production in the cells was monitored with a flow cytometer (Becton Dickinson, San Jose, CA, USA) and the Cell-Quest Pro software .
Detection of apoptotic sub-G1 hypodiploid cells
Harvested cells were fixed in 75% ethanol at 4°C for 30 min and incubated at room temperature for 30 min in the dark in PBS containing PI and RNase A. Sub-G1 hypodiploid cells were assessed using a flow cytometer.
Assessment of apoptosis by flow cytometry
To assess the induced cell apoptosis rate quantitatively, a fluorescein-conjugated Annexin V (Annexin V-FITC) staining assay was performed according to the manufacturer’s protocol (BD Biosciences Pharmingen, San Jose, CA, USA). Briefly, cells were stained with 5 μl Annexin V-FITC and 5 μl PI in each sample. After incubation for 15 min at room temperature in the dark, the degree of apoptosis was quantified as a percentage of the Annexin V-positive and PI-negative cells by flow cytometry.
Data are expressed as means ± standard error of the mean (SEM). The results were subjected to an analysis of variance using Tukey’s test to analyze differences. A p value < 0.05 was considered to indicate statistical significance.
SHME increases the viability of H2O2-treated C2C12 cells
SHME attenuates H2O2-induced apoptosis in C2C12 cells
SHME reduces H2O2-mediated DNA damage
SHME upregulates HO-1 and Nrf2 protein expression
HO-1 is involved in SHME protection against H2O2 treatment
The antioxidative effects and bioactivities of several different crude extracts and certain components of various marine algae have been evaluated both in vitro and in vivo. Because oxidative stress plays important roles in the occurrence and progress of various human diseases, natural marine algal products are attractive targets for the development of novel health-promoting agents [12,13]. In this study, as part of our screening program for therapeutic antioxidative agents from seaweeds, we investigated whether SHME, a methanol extract derived from S. horneri, had protective effects against H2O2-induced cytotoxicity in C2C12 cells.
Generally, mild ROS conditions stimulate cellular antioxidant systems, which protect against oxidative stress, but extreme ROS can destroy the cytoprotective defense mechanisms, such as antioxidant and DNA repair systems. Such oxidative damage to cells ultimately leads to cell death, including programmed cell death or apoptosis [9-11]. In the present study, C2C12 cells exposed to H2O2 exhibited significantly decreased cell viability and increased apoptosis. Notably, SHME increased cell viability significantly by inhibiting H2O2-induced apoptosis and reduced ROS generation generated by H2O2 treatment in C2C12 cells (Figures 2 and 3). Additionally, H2O2 treatment increased the expression of p-γH2A.X, an indicator of DSB formation , and DNA tail length in the comet assay, whereas each event was mitigated in C2C12 cells by treatment with SHME prior to H2O2 exposure (Figure 4). These results suggest that the SHME protected cellular DNA against oxidative stress damage.
Among the various antioxidant/cytoprotective enzymes, HO-1 has received considerable attention. HO-1 is readily induced in response to oxidative stress, and the induction of HO-1 results in a relatively higher resistance to oxidative damage. Transcriptional regulation of the HO-1 gene is linked to the transcription factor Nrf2, which plays a key role in cellular defenses [9-11]. Nrf2 is localized in an inactive form in the cytoplasm, where it is anchored by its inhibitor protein, Kelch-like ECH-associated protein 1 (Keap1). In response to oxidative stress, Nrf2 is released from Keap1 and transmits a stress signal to the nucleus for the activation of a distinct set of genes encoding phase II detoxifying enzymes as well as several stress responsive proteins, including HO-1 [7,8]. Therefore, we were further interested in determining the potential role of HO-1 in H2O2-induced C2C12 cell damage and SHME-mediated cytoprotection. We have provided evidence for the induction of HO-1 by SHME and showed that SHME-induced HO-1 protein expression occurred in a concentration- and time-dependent manner, with a concomitant increase in Nrf2 expression (Figure 5). We further confirmed that exogenous induction of HO-1 by SHME was useful in H2O2-induced oxidative damage of C2C12 cells. Our data indicate that inhibiting HO-1 function using the HO-1 inhibitor ZnPP effectively reduced the protective effect of the SHME against H2O2-induced DNA damage (Figure 6) as well as cytoprotection and ROS generation (Figure 7). The present results demonstrate that the induction of HO-1 by SHME was responsible for protecting C2C12 cells against H2O2-induced oxidative stress, consistent with other studies showing that HO-1 plays an important role protecting cells against oxidative stress [25,26]. The results also suggest that SHME-induced cytoprotection of C2C12 cells against oxidative stress was critically dependent on activation of the Nrf2/HO-1 pathway.
Taken together, our results suggest that SHME may have multiple mechanisms of action against oxidative damage that affect cytoprotection both by reducing ROS generation and boosting HO-1 induction for ROS detoxification. These results support the potential therapeutic mechanism of SHME in protecting against oxidative stress-related diseases with additional research using experimental in vivo disease models.
This work was supported by the R&D program of MOTIE/KIAT (10040391, Development of Functional Food Materials and Device for Prevention of Aging-associated Muscle Function Decrease) and Blue-Bio Industry Regional Innovation Center (RIC08-06-07) at Dongeui University as a RIC program under Ministry of Trade, Industry & Energy and Busan city.
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