Activation of neutral-sphingomyelinase, MAPKs, and p75 NTR-mediating caffeic acid phenethyl ester–induced apoptosis in C6 glioma cells
© Tseng et al.; licensee BioMed Central Ltd. 2014
Received: 25 March 2014
Accepted: 25 June 2014
Published: 5 July 2014
Caffeic acid phenethyl ester (CAPE), a component of propolis, is reported to possess anti-inflammatory, anti-bacterial, anti-viral, and anti-tumor activities. Previously, our laboratory demonstrated the in vitro and in vivo bioactivity of CAPE and addressed the role of p53 and the p38 mitogen-activated protein kinase (MAPK) pathway in regulating CAPE-induced apoptosis in C6 glioma cells.
C6 cancer cell lines were exposed to doses of CAPE; DNA fragmentation and MAPKs and NGF/P75NTR levels were then determined. SMase activity and ceramide content measurement as well as western blotting analyses were performed to clarify molecular changes. The present study showed that CAPE activated neutral sphingomyelinase (N-SMase), which led to the ceramide-mediated activation of MAPKs, including extracellular signal-regulated kinase (ERK), Jun N-terminus kinase (JNK), and p38 MAPK. In addition, CAPE increased the expression of nerve growth factor (NGF) and p75 neurotrophin receptor (p75NTR). The addition of an N-SMase inhibitor, GW4869, established that NGF/p75NTR was the downstream target of N-SMase/ceramide. Pretreatment with MAPK inhibitors demonstrated that MEK/ERK and JNK acted upstream and downstream, respectively, of NGF/p75NTR. Additionally, CAPE-induced caspase 3 activation and poly [ADP-ribose] polymerase cleavage were reduced by pretreatment with MAPK inhibitors, a p75NTR peptide antagonist, or GW4869.
Taken together, N-SMase activation played a pivotal role in CAPE-induced apoptosis by activation of the p38 MAPK pathway and NGF/p75NTR may explain a new role of CAPE induced apoptosis in C6 glioma.
Caffeic acid phenethyl ester (CAPE) is secondary products of propolis and thus possesses anti-oxidant, anti-angiogenic, anti-viral, anti-inflammatory, and anti-metastatic properties. CAPE also selectively represses the proliferation of several types of carcinoma cells, but show almost no toxic effects on normal peripheral blood cells or on normal hepatocytes [1–6]. Studies of previous studies have revealed a broad spectrum of biological activities that CAPE induced apoptosis in oral cancer cells and glioma cells [7, 8]. In in vitro and in vivo studies, CAPE inhibited the proliferation of C6 glioma cells . Further, CAPE enhanced all-trans retinoic acid-induced differentiation in human leukemia HL-60 cells . The mitogen-activated protein kinases (MAPKs) are a family of protein kinases that comprise a diverse superfamily of phylogenetically conserved serine/threonine kinases. There are three classical MAP kinase families: c-Jun N-terminal kinases (JNKs), Ras/extracellular signal-regulated kinase (ERK), and p38 MAPK. Although it is previously showed that activation of ERK1/2 leads to cell growth, ERK1/2 activation results in cell apoptosis under some conditions [11, 12]. JNK1/2 and p38 MAPK are highly effected in signalling to various stress signals, including TNFα, oxidative stress, and ultraviolet (UV) light. Their activation is most frequently associated with the induction of apoptosis [13, 14]. Our previous study showed that CAPE caused p53-dependent apoptosis in C6 glioma cells through the p38 MAPK signaling pathway . In addition to activating p38 MAPK in C6 glioma cells, CAPE increased the phosphorylation of ERK and JNK, whose involvement was previously unknown.
Nerve growth factor (NGF) regulates neurotrophic actions on many neurons in rats . NGF are involved a surprising variety of neurons, glia, and nonneural cells by a high-affinity receptor TrkA and a low-affinity receptor, p75 neurotrophin receptor (p75NTR) . TrkA and p75NTR collaborate to essentially takes place upon the binding to the cell surface as neurotrophins . It is now thought that p75NTR play a crucial role in the glioma apoptotic pathway . p75NTR cognate TNFα superfamily receptors Fas and CD40 are expressed in tissues to which these glioma cells commonly death .
Three mammalian isoforms of neutral sphingomyelinase (N-SMase) have been cloned to date. N-SMase is membrane-bound and Mg2+-dependent. Acidic sphingomyelinase (A-SMase) has three isoforms, an endosomal lysosomal A-SMase, a secretory Zn2+-dependent A-SMase, and a receptor-activated A-SMase . A ceramide is composed of sphingosine and a fatty acid that serves as a proapoptotic molecule . Ceramide has been involved in a variety of physiological functions including apoptosis, cell growth arrest, differentiation, cell migration and adhesion. Several studies have attempted to define the roles of SMase and ceramide on induction of NGF synthesis in primary astrocyte cultures, indicating it may be crosstalk between ceramide and NGF receptor (NGFR) signaling in the nervous cells . Further, N-SMase plays a role in chemotherapy-mediated cell death. In the present study, we examined whether SMase/ceramide induced up-regulation of NGF/p75NTR is mediated by CAPE-induced apoptosis, and we clarified the relationship between SMase/ceramide, NGF/p75NTR, and the MAPK signaling pathway in C6 glioma cells.
Chemical reagents and antibodies
All culture materials were purchased from Invitrogen (Carlsbad, CA). The Amplex Red Sphingomyelinase kit was purchased from Sigma (St. Louis, MO, USA). Sodium dodecyl sulfide (SDS), bis-acrylamide, ammonium persulfate, N,N,N’,N’-tetramethylethylenediamine (TEMED), and nitrocellulose (NC) paper were from Bio-Rad (Hercules, CA). Caffeic acid phenethyl ester, Triton X-100, Tris base, β-actin antibody, non-hydroxy fatty acid ceramide, and 4’,6-diamidino-2-phenylindole (DAPI) were from Sigma (St. Louis, MO). GW4869, a specific inhibitor of N-SMase, was also purchased from Sigma. Antibodies against NGF, p75NTR, Trk, poly [ADP-ribose] polymerase (PARP), and caspase-3 were from Santa Cruz Biotechnology (Santa Cruz, CA). The p75 antagonist peptide YCDIKGKECY (the cysteine-cysteine bond that results in cyclization is underlined), which is reportedly specific to p75NTR, was synthesized by Protech Technology (Reno, NV) to a minimum of 90% purity . High-performance thin-layer chromatography (HPTLC) silica gel 60 plates were obtained from Merck (Whitehouse Station, NJ).
The rat C6 glioma cell line was originally derived from an N-nitrosomethylurea-induced rat brain tumor . Cells were cultured in minimal essential medium supplemented with 10% fetal calf serum and antibiotics (100 U/ml of penicillin and 100 mg/ml of streptomycin) at 37°C in a humidified atmosphere of 5% CO2 and 95% air. All experiments were performed in plastic tissue culture flasks and dishes or in microplates (Nunc, Naperville, Denmark).
Assessment of cell viability
Cell viability was assessed with the MTT colorimetric assay. The cells were seeded at 2 × 104 cells/ml and incubated with various concentrations of CAPE (0, 5, 10, 25, 50, and 100 μM) for 24 and 48 h. The medium was changed, and the cells were incubated with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT; 0.5 mg/ml) for 4 hr. The viable cell number was directly proportional to the production of formazan, which was solubilized with isopropanol and measured spectrophotometrically at 563 nm.
Analysis of DNA fragmentation
C6 glioma cells cultured in 100-mm dishes were resuspended in 200 ml of hypotonic lysis buffer (0.2% Triton X-100, 1 mM ethylenediaminetetraacetic acid (EDTA), 10 mM Tris–HCl, pH 7.5) and incubated for 20 min at 4°C. After centrifugation for 5 min at 14,000 × g, the supernatant was collected, incubated with RNase A (400 mg/ml) for 30 min at 37°C, and digested with proteinase K (200 mg/ml) for 30 min at 50°C. The fragmented DNA was then precipitated overnight at −20°C in 50% isopropanol and 0.5 M NaCl and centrifuged for 10 min at 14,000 × g. The dried pellets were dissolved in 20 ml of ultra-pure water, and DNA was separated by electrophoresis on a 1.8% agarose gel at 50 V for 1 h.
Preparation of total cell extracts and immunoblot analysis
Cells were plated on 10-cm2 dishes at a density of 1 × 106 cells/ml in the presence or absence of CAPE (50 μM) for 0–24 h and harvested. To prepare whole-cell extracts, cells were washed with phosphate-buffered saline (PBS) plus zinc ion (1 mM) and suspended in lysis buffer (50 mM Tris, 5 mM EDTA, 150 mM NaCl, 1% NP-40, 0.5% deoxycholic acid, 1 mM sodium orthovanadate, 81 μg/ml aprotinin, 170 mg/ml leupeptin, 100 mg/ml phenylmethylsulfonyl fluoride (PMSF); pH 7.5). Lysates were mixed for 30 min at 4°C and centrifuged at 10,000 × g for 10 min. The supernatants were collected as whole-cell extracts. The protein content was determined with Bio-Rad protein assay reagent using bovine serum albumin as a standard. Western blotting with enhanced chemiluminescence (ECL) detection was performed as follows. Total cell lysates with equal protein content from control and CAPE-treated samples was resolved on 8%–12% SDS-PAGE gels along with a prestained protein molecular weight standard (Bio-Rad). Proteins were then blotted onto NC membranes (Sartorious) and reacted with primary antibodies (anti-caspase-3, anti-PARP, anti-Trk, anti-NGF, anti-p75, anti-ERKs, anti-JNKs, anti-p38 MAPK, anti-phosphoserine, anti-phospho-ERKs (Thr183/Tyr185), anti-phospho-JNKs (Thr183/Tyr185), and anti-phospho-p38 (Thr180/Tyr182), and anti-phospho-Trk from Santa Cruz Biotechnology (Santa Cruz, CA); anti-β-actin from Sigma as an internal control). The secondary antibody was a peroxidase-conjugated goat anti-mouse antibody. After antibody binding, the bands were visualized using a commercial ECL kit.
SMase activity assay
SMase activity was analyzed with an Amplex Red Sphingomyelinase Assay Kit. Cells were washed with PBS and pelleted by centrifugation at 1500 × g for 10 min at 4°C. The cell pellet was resuspended, lysed in buffer containing 1% Triton X-100, 1 μg/ml aprotinin, 1 mM EDTA, and 100 μg/ml PMSF for 60 min on ice, and then centrifuged at 17,000 × g for 10 min at 4°C to remove the nuclei. The protein concentration in the supernatant was measured with the Bio-Rad Protein Assay. To analyze the activity of N-SMase, the supernatant was diluted with 1× reaction buffer containing 0.1 M Tris–HCl and 10 mM MgCl2, pH 7.4, and then inoculated into 96-well plates (100 μl/well). The total amount of protein in each well was 25 μg. The solution was added to 100 μl of working solution (containing 8 U/ml alkaline phosphatase, 0.2 U/ml choline oxidase, 2 U/ml horseradish peroxidase, and 0.5 mM sphingomyelin) and incubated for 45 min at 37°C. The H2O2 generated reacted with Amplex Red to elicit fluorescent resorufin. The fluorescent intensity was measured with a fluorescence multi-well reader (HTS 7000) immediately at excitation/emission wavelengths of 571/585 nm. Acid sphingomyelinase (A-SMase) activity was analyzed with a two-step assay. First, the supernatant was diluted with 50 mM sodium acetate (not 1× reaction buffer), and 100 μl of the diluted supernatant was inoculated to each well of a 96-well plate. To generate phosphorylcholine and ceramide, 10 μl of 5 mM sphingomyelin solution was added to each well and then incubated for 1 h at 37°C. Working solution (100 μl) containing 8 U/ml alkaline phosphatase, 0.2 U/ml choline oxidase, and 2 U/ml horseradish peroxidase was then added to each well and reacted with phosphorylcholine for 45 min at 37°C. The H2O2 generated from the two-step procedure then reacted with Amplex Red to elicit resorufin, which was measured with a fluorescence multi-well reader as described above.
Quantitative measurement of ceramide content
Cells were harvested in lysis buffer containing 50 mM Tris–HCl, pH 6.8, 10% glycerol, 2% SDS, and 5% β-mercaptoethanol and vortexed for 1 hr at 4°C. The lipids were extracted by the following procedure. In brief, 1 ml of cell lysate was suspended with 1.25 ml of chloroform and 2.5 ml of methanol, vortexed, and incubated overnight at 4°C. After centrifugation for 5 min at 1700 × g, 1.25 ml of chloroform and 1.25 ml of 0.88% KCl were added to the supernatant. The tubes were then vortexed and centrifuged for 5 min at 1700 × g. The organic lower phase was transferred to a fresh tube and evaporated. The lipids were dissolved into chloroform-methanol [2:1 (v/v)] and analyzed using an HPTLC silica gel 60 plate. Dichloromethane-methanol-glacial acetic acid [100:2:5 (v/v)] was used to separate the lipid. Individual lipid classes were visualized by dipping each plate into CuSO4 (3%)/H3PO4 (8%) for 30 sec. The plate was then incubated in an oven at 180°C for 10 min. The bands were scanned and the data were evaluated with an LAS-3000 imager (Fuji Photo Film Co., Ltd., Tokyo, Japan). In addition to the three sample replicates, C2-ceramide was added to each plate as the lipid standard.
Determining the effects of MAPK inhibitors, SMase inhibitors, and a p75NTR antibody inhibitor
C6 glioma cells were pretreated with 50 μM PD98059, 5 μM SB203580, 10 μM SP600125, 10 or 20 μM GW4869, or a p75NTR antibody inhibitor for 1 hr and then treated with 50 μM CAPE for 0–24 hr. The cell extracts were analyzed by immunoblotting with specific antibodies (anti-CPP32, anti-PARP, anti-NGF, anti-p75, anti-ERKs, anti-JNKs, anti-p38 MAPK, anti-phosphoserine, anti-phospho-ERKs (Thr183/Tyr185), anti-phospho-JNKs (Thr183/Tyr185), and anti-phospho-p38 (Thr180/Tyr182), as previously described.
We used DAPI staining to assess morphological changes in chromatin structure in C6 glioma cells undergoing apoptosis. Cells were trypsinized, mounted on glass slides, fixed in 4% paraformaldehyde for 30 min, and stained with 1 μg/ml DAPI for 30 min. Apoptosis was characterized by chromatin condensation and fragmentation, which were visualized with fluorescence microscopy.
Data were reported as the mean ± SD of three independent experiments and evaluated by one-way ANOVA. Differences were considered significant at P < 0.05.
Involvement of MAPKs in CAPE-mediated caspase 3 activation and PARP cleavage
Involvement of NGF/p75NTR in CAPE-mediated caspase 3 activation and PARP cleavage
Association of MAPKs and NGF/p75NTR after treatment with CAPE
Activation of N-SMase by CAPE
MAPKs and NGF/p75NTR signal downstream of N-SMase
CAPE induces apoptosis through N-SMase activation
Apoptosis, an active process that leads to cell death, is mediated by programmed signaling pathways that can be initiated by various extracellular or intracellular stimuli. The ability to efficiently induce apoptosis is essential for the development of effective cancer therapies. In the present study, we demonstrated that CAPE-induced apoptosis involves the activation of N-SMase and the accumulation of ceramide. Blocking the activation of N-SMase decreased CAPE-induced caspase 3 activation and PARP cleavage. These results demonstrate the pivotal role of N-SMase in CAPE-induced apoptosis. SMases are activated in response to several stimuli . In particular, the neutral Mg2+-dependent N-SMase is regulated by glutathione (GSH) . Moreover, the reduction in cellular GSH levels induced by TNF-α signaling activates N-SMase . Consistently, in our study, GSH was depleted in CAPE-treated C6 glioma cells (data not shown), and N-SMase was activated. However, the mechanism by which CAPE reduces GSH levels requires further investigation.
p75NTR induces cell death in primary trigeminal, sympathetic neurons as well as in Schwann and neuroblastoma cells. The signaling events that link p75NTR activation to apoptosis have begun to emerge. p75NTR-dependent apoptosis is associated with an increase in JNK activity and caspase activation [27, 28]. Consistently, our results demonstrated that CAPE-induced p75NTR expression was associated with the activation of JNK and caspase 3. CAPE increased the expression of p75NTR, but not TrkA, within 6 h. The rapid increase in p75NTR might be regulated at the translational or post-translational level. However, it might also result from a decrease in p75NTR degradation, which may occur under physiological conditions. On the other hand, the NGF level also increased after treatment with CAPE. NGF exerts different effects by binding with its receptors, TrkA and p75NTR. TrkA transduces NGF signals for survival and differentiation, whereas p75NTR induces cell death. The increase in NGF and p75NTR shown in the present study indicates an amplification of apoptotic signals.
Our previous paper demonstrated that CAPE activated p38 MAPK and that p38 kinase formed a complex with p53, resulting in the release of cytochrome C after treatment with CAPE for 0.5 h. Furthermore, we suggest that N-SMase/ceramide is the upstream target of p38 MAPK. Increasing the apoptotic potential of cancer cells through rational manipulation of ceramide levels may improve the efficacy of chemotherapy agents. Although CAPE induces apoptosis in C6 glioma cells by activating multiple signaling pathways (Figure 7), the activation of N-SMase/ceramide plays an essential role. In conclusion, the N-SMase/ceramide pathway is an important target of novel chemotherapy agents for the treatment of glioma.Our previous paper demonstrated that CAPE activated p38 MAPK and that p38 kinase formed a complex with p53, resulting in the release of cytochrome C after treatment with CAPE for 0.5 h. Furthermore, we suggest that N-SMase/ceramide is the upstream target of p38 MAPK. Increasing the apoptotic potential of cancer cells through rational manipulation of ceramide levels may improve the efficacy of chemotherapy agents. Although CAPE induces apoptosis in C6 glioma cells by activating multiple signaling pathways (Figure 7), the activation of N-SMase/ceramide plays an essential role. In conclusion, the N-SMase/ceramide pathway is an important target of novel chemotherapy agents for the treatment of glioma.
This study was supported by grants CSMU-INT-102-16, CZRPG880253, CMRPF6A0073, CMRPF6C0032, and EZRPF6C0011 from Chung Shan Medical University, Chang Gung Memorial Hospital, and Chang Gung University of Science and Technology, Chia-Yi Campus, Taiwan and by the National Science Council and Ministry of Science and Technology, Taiwan (NSC100-2320-B-040-006, NSC101-2622-B-255-001-CC3, NSC102-2313-B-255-002 and MOST103-2622-B-255-001-CC3).
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