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GSK-3β-mediated regulation of cadmium-induced cell death and survival
Cellular & Molecular Biology Letters volume 23, Article number: 9 (2018)
Previous studies indicated that cadmium (Cd) increases PI3-kinase/Akt phosphorylation, resulting in an alteration in GSK-3β activity. However, the mechanism of Cd-induced endoplasmic reticulum (ER) stress in neuronal cells has yet to be studied in needs further elucidation. We examined the role of GSK-3β in Cd-induced neuronal cell death and the related downstream signaling pathways.
SH-SY5Y human neuroblastoma cells were treated with 10 or 20 μM BAPTA-AM and 1 μM wortmannin for 30 min and then incubated with 25 μM Cd for 12 h. Apoptotic cells were visualized via DAPI and PI staining. Data were evaluated with one-way analysis of variance (ANOVA) followed by Student’s t-test. Data are expressed as the means ± SD of experiments performed at least three times.
Treatment of human neuronal SH-SY5Y cells with Cd induced ER, stress as evidenced by the increased expression of GRP78, which is a marker of ER stress. Cd exposure significantly increased the phosphorylation of Akt at thr308 and ser473 and that of GSK-3β at ser9 in a time-dependent manner, while the total protein levels of GSK-3β and Akt did not change. Cd-induced apoptosis was higher in GSK-3β-knockdown cells than in normal cells.
Our data suggest that Akt/GSK-3β signaling activated by Cd is involved in neuronal cell survival.
Cadmium (Cd) is a potent toxic metal that affects various cellular processes, such as cell proliferation and apoptosis. It can cause DNA damage, reactive oxygen species (ROS) production and endoplasmic reticulum (ER) stress [1, 2]. The latter two events are important triggers of the stress response in many cell types [1,2,3].
In neuronal cells, Cd activates c-Jun N-terminal kinase (JNK) or p38 through ROS production, resulting in apoptosis [3,4,5,6]. However, the signaling pathways involved in Cd-induced ER stress and apoptosis in neurons are poorly understood.
Previously, we found that Cd induces neuronal cell death through ROS production activated by GADD153. The exposure of SH-SY5Y cells to Cd led to an increase in intracellular GADD153 and Bak levels in dose- and time-dependent manners .
The ER regulates protein synthesis, folding and tracking , and is highly sensitive to alterations in calcium homeostasis and perturbations of its intralumenal environment. Calcium ionophores, ER Ca2+-ATPase inhibitors (e.g., thapsigargin), protein glycosylation inhibitors (e.g., tunicamycin) and misfolded proteins can all disrupt ER function. In response to such ER stresses, protective signal transduction mechanisms such as the induction of glucose-regulated protein 78 (GRP78) [6, 7] or molecular chaperones of the heat shock protein (Hsp70) family are activated. Alternatively, an apoptotic pathway may be initiated, via the activation of transcription factor GADD 153/CHOP or the ER-resident cysteine protease, caspase-12 [7, 9, 10]. Thus, ER stress has been linked to neurodegenerative diseases such as cerebral ischemia  and Alzheimer’s disease , which involve neuronal apoptosis. Autopsy studies suggest that the PERK-EIF2α pathway is hyperactive in the brains of patients with Alzheimer’s disease , implying the presence of ER stress.
Glycogen synthase kinase-3 (GSK-3) is a ubiquitously expressed serine/threonine kinase that regulates glycogen synthesis and controls multiple cell signaling pathways [14, 15]. Two mammalian GSK-3 isoforms, GSK-3α (51 kDa) and GSK-3β (47 kDa), are highly similar and share substrate specificity in vitro, but are encoded by different genes . GSK-3β is a constitutive active kinase that regulates many intracellular signaling pathways by phosphorylating substrates such as β-catenin , cAMP response element-binding protein (CREB)  and tau  in SH-SY5Y cells. GSK-3β activity is regulated through its phosphorylation by other protein kinases, including Akt. For example, in response to insulin and growth factor stimulation, GSK-3β activity is negatively regulated by phosphorylation at serine 9 (Ser9) by the survival-promoting kinase Akt, which is activated in response to various mitogens and growth factors. Other phosphorylation sites are threonine 390 and thyrosine 216 in GSK-3β, the activities of which are respectively negatively and positively regulated [20, 21].
There is evidence that Cd increases PI3-kinase/Akt phosphorylation , resulting in an alteration in GSK-3β activity. However, the mechanism of Cd-induced ER stress in neuronal cells has yet to be studied in needs further elucidation. Here, we investigated the role of intracellular calcium and Cd-induced ER stress in the regulation of GSK-3β activity.
Materials and methods
Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine serum (FBS) and antibiotics were purchased from Gibco BRL. Cadmium chloride (Cd), Nonidet-P40 (NP-40), wortmannin (PI3K inhibitor), thapsigargin (Ca2+-ATPase inhibitor) and N-acetyl-L-cysteine (NAC) were obtained from Sigma. [1,2-bis(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid tetrakis (acetoxy methyl ester)] BAPTA-AM (a Ca2+ Chelator) was obtained from Calbiochem-Novabiochem. GSK-3β antibodies were obtained from Cell Signaling Technology. GRP78, GRP94 and GADD153 were obtained from BD Biosciences.
SH-SY5Y cell culture
SH-SY5Y human neuroblastoma cells (ATCC CRL-2266) were cultured in DMEM supplemented with 10% FBS, 100 U/ml penicillin, 100 mg/ml streptomycin and 0.25 mg/ml amphotericin B. Cells were maintained at 37 °C in a humidified atmosphere of 95% air/5% CO2.
Western blot analysis
Cells were lysed in RIPA buffer consisting of 50 mM Tris-HCl (pH 7.5), 1% NP-40, 0.5% sodium deoxycholic acid and 0.1% SDS with proteinase inhibitors: 1 mM phenylmethylsulfonyl fluoride, 2 μg/ml aprotinin and 2 μg/ml leupeptin. Cellular debris was removed by centrifugation at 12,000×g for 20 min. An aliquot (40 μg) of the total protein was separated using 12.5% SDS-PAGE, and the proteins were transferred onto a nitrocellulose membrane (Amersham Bioscience). After the membrane was blocked with 5% fat-free milk in TBST buffer consisting of 25 mM Tris-HCl (pH 7.4), 137 mM NaCl, 5 mM KCl and 0.2% Tween 20 for 1 h, it was incubated with the appropriate primary and secondary antibodies for 1 h each and then developed using an enhanced chemiluminescence kit from Amersham Bioscience. All antibodies were used at a dilution of 1:1000.
Cells were treated with 25 μM Cd for the indicated times, then washed with phosphate-buffered saline (PBS), harvested using trypsin, suspended in PBS, and incubated with 4 μM fluo-4 at 37 °C for 1 h. The cells were centrifuged at 1000×g for 5 min, washed three times with PBS, resuspended in PBS, and incubated at 37 °C for 20 min. Intracellular Ca2+ was analyzed using flow cytometry (FACSCanto; BD Biosciences).
DAPI staining and annexin V assay
Cells were treated with 10 or 20 μM BAPTA-AM for 30 min and then incubated with 25 μM Cd for 12 h. The cells were washed with PBS, fixed for 30 min with 4% paraformaldehyde (PFA) prepared in PBS, treated with RNase (1 mg/ml), and incubated with 4′,6-diamindine-2-phenilindole (DAPI; 10 μg/ml) for 30 min. Apoptotic cells with condensed or fragmented nuclei were visualized under a fluorescence microscope. Approximately 100–200 cells per well were assessed. Apoptotic cells were detected by annexin V binding using a kit from Molecular Probes, Inc. according to the manufacturer’s instructions.
Cell staining with propidium iodide
Cells were treated with 1 μM wortmannin for 30 min and then incubated with 25 μM Cd for 12 h. The cells were washed with PBS, harvested using trypsin and stained with propidium iodide (PI; 5 μg/ml). The cells were analyzed using flow cytometry (FACSCanto; BD Biosciences) and the extent of apoptosis was determined based on the sub-G1 population.
Data were evaluated with one-way analysis of variance (ANOVA) followed by Student’s t-test. The data are expressed as the means ± SD of experiments performed at least three times. Statistically significant differences are reported as *p < 0.05, **p < 0.01 or ***p < 0.001. Data with values of p < 0.05 were generally accepted as statistically significant.
Cd induces neuronal cell apoptosis through ER stress
Cd induces cell death in many cell types . To assess Cd-induced apoptosis in human neuronal cells, SH-SY5Y cells were treated with 25 μM Cd for 0, 6, 12, 18 and 24 h. Nuclear staining with the fluorescent dye DAPI were revealed chromatin condensation and fragmentation in the Cd-treated cells (data not shown).
To determine whether Cd induces ER stress in SH-SY5Y cells, we examined the protein expression levels of three ER stress markers, GRP78, GRP94 and GADD153, after Cd treatment. The expression levels of GRP78 and GADD153 had increased and this increase was sustained for up to 24 h after Cd treatment (Fig. 1). The expression of GRP94 and β-actin had not changed following Cd treatment. Cells treated with thapsigargin (TG; 1 μM for 6 ~ 24 h) as a positive control for ER stress showed an increase in the cellular GRP78 protein level after 12 h (Fig. 1). These results are consistent with earlier results  suggesting that Cd induces not only ROS but also ER stress in neuronal cells.
The observable increase in cytoplasmic Ca2+ results from either an influx from the extracellular environment or efflux from intracellular ER stores, and is associated with the initiation of apoptosis in diverse in vivo and in vitro systems . To investigate the role of intracellular Ca2+ in Cd-induced ER stress, Ca2+ was measured over time via flow cytometry using the calcium indicator dye fluo-4 (Fig. 2a). Intracellular Ca2+ was significantly elevated after Cd treatment, increasing as early as 0.5 h after exposure. It oscillated, but reached a peak of around 8-fold higher than the baseline 18 h after Cd exposure. However, the increase in intracellular Ca2+ was blocked by pretreatment with 10 μM BAPTA-AM, a Ca2+ chelator. To examine the increase in intracellular Ca2+ associated with ER stress, the GRP78 protein level was assessed in cells pretreated with BAPTA-AM. As shown in Fig. 2b, Cd-induced upregulation of GRP78 was not inhibited by the Ca2+ chelator. In comparison, the apoptosis assay using annexin V were revealed that the pretreatment of cells with 10 μM BAPTA-AM did not protect cells significantly from Cd-mediated apoptosis (Fig. 2c). This result indicates that ER stress, which induces upregulation of GRP78, may play an important role in Cd-induced apoptotic cell death, but that the apoptotic pathway was independent of the intracellular Ca2+ level.
Cd increases GSK-3β phosphorylation via Akt
GSK-3β is a serine/threonine protein kinase known for its role in neuropathological disorders. In response to p90rsk1 and MEK1/2, GSK-3β is phosphorylated at ser9 to negatively regulate its activity or at tyrosine 216 (tyr216) to positively regulate its activity . Using an antibody directed against phospho-ser9, we examined whether Cd induced GSK-3β phosphorylation at ser9 in SH-SY5Y cells. Figure 3a shows that the phosphorylation of Akt at thr308 and ser473 and that of GSK-3β at ser9 were significantly increased by exposure to 25 μM Cd in a time-dependent manner, while the total protein levels of GSK-3β and Akt did not change. Thus, Cd negatively regulates GSK-3β activity and positively regulates Akt activity.
When cells were pretreated for 30 min with the Ca2+ chelator BAPTA-AM (10 μM) before treatment with 25 μM Cd, the Cd-induced upregulation of Akt and GSK-3β phosphorylation was found to have significantly decreased (Fig. 3b). When Akt activation was inhibited by wortmannin, the phosphorylation levels of both Akt (at thr308) and GSK-3β (at ser9) were significantly lower than those found when was used Cd alone (Fig. 3c). These results suggest that Cd inactivates GSK-3β through Akt activation. When neuronal cells were treated with wortmannin for 30 min before treatment with 25 μM Cd for 12 h, the number of apoptotic cells was significantly higher than for cells with no pretreatment (Fig. 3d). These findings indicate that the Akt/GSK-3β pathway plays a survival role in Cd-induced cell death in SH-SY5Y cells.
Knockdown of GSK-3β increases cd-induced apoptosis
Several studies have proposed that GSK-3β activation results in apoptosis. Although Cd induced increases in the phosphorylation of Akt and GSK-3β (Fig. 3a), the role of GSK-3β in Cd-induced apoptosis in SH-SY5Y cells was unclear. To investigate this, cells were transfected with small interfering RNA (siRNA) targeted against the GSK-3β coding region and then treated with Cd. Cd-induced apoptosis was increased in GSK-3β-knockdown cells compared to the level for normal cells (Fig. 4a and b). These results suggest that GSK-3β is likely to be a signal leading to cell death.
Discussion and conclusions
Owing to its central role in the induction of multiple signaling pathways, Ca2+ is crucial for the sustainability of biological functions, including learning and memory, fertilization, proliferation, development and cell death . Li et al. reported that Cd is a potent Ca2+ channel blocker that inhibits cellular Ca2+ uptake . By contrast, Cd also increases intracellular Ca2+ by inhibiting Ca2+-ATPase in the ER membrane. In addition, Cd activates some calcium-related enzymes such as protein kinase C , mitogen-activated protein kinase  and calmodulin-dependent kinase . Furthermore, the elevation of intracellular Ca2+ has been reported to disrupt mitochondrial Ca2+ equilibrium, resulting in the formation of ROS .
Recent studies have shown that an increase in intracellular Ca2+ attributable to Ca2+ release from the ER leads to the activation of calpain proteases and caspase-12, which leads in turn to cell death [25, 30]. Our previous data showed that SH-SY5Y cells with NAC showed reduced nuclear fragmentation and condensation and caspase activation . NAC did not affect the regulation of GRP78 or GSK-3β. However, BAPTA-AM significantly inhibited the activity of GSK-3β, demonstrating that Cd-induced ROS generation was not required for ER stress and that GSK-3β played a central role in the regulation of apoptosis. This discrepancy indicates marked differences in the regulation of stress responses (i.e., oxidative stress due to ROS vs. ER stress) depending on the cell type and stimulus.
GSK-3β is key node in modulating substrate recognition and kinase activity, which is inhibited by pro-survival PI3K-AKT signaling. Activated Akt plays a survival role in many cell types , whereas GSK-3β has a death signaling role after induction by other extracellular stimuli [32, 33]. In previous studies, Cd has been shown to increase Akt phosphorylation [34,35,36]. In this study, Cd increased Akt and GSK-3β phosphorylation, and an Akt inhibitor, wortmannin, decreased both Akt and GSK-3β phosphorylation (Fig. 3). Thus, Cd decreased GSK-3β activity through increased Akt phosphorylation. In addition, Cd-induced apoptosis was increased by wortmannin pretreatment and GSK-3β siRNA. These results suggest that the role of GSK-3β is not apoptosis but that the survival signal in Cd induces an increase in intracellular Ca2+ (Fig. 5).
The pro-survival activity of GSK-3 through NF-kB has been shown to play a role in chronic lymphocytic leukemia (CLL) . GSK-3 activity also contributes to pro-survival NF-kB signaling through the phosphorylation of the NF-kB inhibitory protein p100. GSK-3β is crucially involved in many signaling pathways. Its role in the regulation of apoptosis is not constant, and in some situations GSK-3β promotes cell survival .
In early ER stress, translational attenuation occurs to reduce the ER load. During the next phase, several groups of genes are transcriptionally induced for long-term adaptation to ER stress. If severe ER stress conditions persist, apoptosis signaling pathways are activated, including induction of CHOP and activation of JNK and caspase-12. Thus, the influence of ER stress on cell death and survival depends on the balance between apoptosis and survival .
These results provide evidence that Cd-induced apoptosis of neuronal cells is mediated, at least in part, by ER stress, and that regulation via a distinct GSK-3β pathway is implicated in the apoptotic process. As demonstrated in this study, Cd can produce both pro- and anti-apoptosis signals, although under the conditions of our experiments, Cd treatment ultimately resulted in apoptosis.
Glycogen synthase kinase-3 β
Kwon OY, Kim YJ, Choi Y, Kim H, Song C, Shong M. The endoplasmic reticulum chaperone GRP94 is induced in the thyrocytes by cadmium. Z Naturforsch C. 1999;54(7–8):573–7.
Timblin CR, Janssen YM, Goldberg JL, Mossman BT. GRP78, HSP72/73, and cJun stress protein levels in lung epithelial cells exposed to asbestos, cadmium, or H2O2. Free Radic Biol Med. 1998;24(4):632–42.
Kim SD, Moon CK, Eun SY, Ryu PD, Jo SA. Identification of ASK1, MKK4, JNK, c-Jun, and caspase-3 as a signaling cascade involved in cadmium-induced neuronal cell apoptosis. Biochem Biophys Res Commun. 2005;328(1):326–34.
Lee SA, Dritschilo A, Jung M. Role of ATM in oxidative stress-mediated c-Jun phosphorylation in response to ionizing radiation and CdCl2. J Biol Chem. 2001;276(15):11783–90.
Rockwell P, Martinez J, Papa L, Gomes E. Redox regulates COX-2 upregulation and cell death in the neuronal response to cadmium. Cell Signal. 2004;16(3):343–53.
Liu H, Bowes RC 3rd, van de Water B, Sillence C, Nagelkerke JF, Stevens JL. Endoplasmic reticulum chaperones GRP78 and calreticulin prevent oxidative stress, Ca2+ disturbances, and cell death in renal epithelial cells. J Biol Chem. 1997;272(35):21751–9.
Kim SW, Cheon HS, Kim SY, Juhnn YS, Kim YY. Cadmium induces neuronal cell death through reactive oxygen species activated by GADD153. BMC Cell Biol. 2013;14(4):1–9.
Rao RV, Ellerby HM, Bredesen DE. Coupling endoplasmic reticulum stress to the cell death program. Cell Death Differ. 2004;11(4):372–80.
Oyadomari S, Koizumi A, Takeda K, Gotoh T, Akira S, Araki E, et al. Targeted disruption of the Chop gene delays endoplasmic reticulum stress-mediated diabetes. J Clin Invest. 2002;109(4):525–32.
Nakagawa T, Zhu H, Morishima N, Li E, Xu J, Yankner BA, et al. Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-beta. Nature. 2000;403(6765):98–103.
Mattson MP, LaFerla FM, Chan SL, Leissring MA, Shepel PN, Geiger JD. Calcium signaling in the ER: its role in neuronal plasticity and neurodegenerative disorders. Trends Neurosci. 2000;23(5):222–9.
Sherman MY, Goldberg AL. Cellular defenses against unfolded proteins: a cell biologist thinks about neurodegenerative diseases. Neuron. 2001;29(1):15–32.
Unterberger U, Hoftberger R, Gelpi E, Flicker H, Budka H, Voigtlander T. Endoplasmic reticulum stress features are prominent in Alzheimer disease but not in prion diseases in vivo. J Neuropathol Exp Neurol. 2006;65(4):348–57.
Doble BW, Woodgett JR. GSK-3: tricks of the trade for a multi-tasking kinase. J Cell Sci. 2003;116(Pt 7):1175–86.
Harwood AJ. Regulation of GSK-3: a cellular multiprocessor. Cell. 2001;105(7):821–4.
Grimes CA, Jope RS. The multifaceted roles of glycogen synthase kinase 3beta in cellular signaling. Prog Neurobiol. 2001;65(4):391–426.
Chong ZZ, Li F, Maiese K. Cellular demise and inflammatory microglial activation during beta-amyloid toxicity are governed by Wnt1 and canonical signaling pathways. Cell Signal. 2007;19(6):1150–62.
Grimes CA, Jope RS. CREB DNA binding activity is inhibited by glycogen synthase kinase-3 beta and facilitated by lithium. J Neurochem. 2001;78(6):1219–32.
Lesort M, Jope RS, Johnson GV. Insulin transiently increases tau phosphorylation: involvement of glycogen synthase kinase-3beta and Fyn tyrosine kinase. J Neurochem. 1999;72(2):576–84.
Bhat RV, Shanley J, Correll MP, Fieles WE, Keith RA, Scott CW, et al. Regulation and localization of tyrosine216 phosphorylation of glycogen synthase kinase-3beta in cellular and animal models of neuronal degeneration. Proc Natl Acad Sci U S A. 2000;297(20):11074–9.
Thornton TM, Pedraza-Alva G, Deng B, Wood CD, Aronshtam A, Clements JL, et al. Phosphorylation by p38 MAPK as an alternative pathway for GSK3beta inactivation. Science. 2008;320(5876):667–70.
Thevenod F. Cadmium and cellular signaling cascades: to be or not to be? Toxicol Appl Pharmacol. 2009;238(3):221–39.
Berridge MJ, Bootman MD, Lipp P. Calcium--a life and death signal. Nature. 1998;395(6703):645–8.
Berridge MJ, Lipp P, Bootman MD. The versatility and universality of calcium signalling. Nat Rev Mol Cell Biol. 2000;1(1):11–21.
Li M, Kondo T, Zhao QL, Li FJ, Tanabe K, Arai Y, et al. Apoptosis induced by cadmium in human lymphoma U937 cells through Ca2+−calpain and caspase-mitochondria- dependent pathways. J Biol Chem. 2000;275(50):39702–9.
Long GJ. The effect of cadmium on cytosolic free calcium, protein kinase C, and collagen synthesis in rat osteosarcoma (ROS 17/2.8) cells. Toxicol Appl Pharmacol. 1997;143(1):189–95.
Wang Z, Templeton DM. Induction of c-fos proto-oncogene in mesangial cells by cadmium. J Biol Chem. 1998;1273(1):73–9.
Kostrzewska A, Sobieszek A. Diverse actions of cadmium on the smooth muscle myosin phosphorylation system. FEBS Lett. 1990;263(2):381–4.
Kim J, Sharma RP. Calcium-mediated activation of c-Jun NH2-terminal kinase (JNK) and apoptosis in response to cadmium in murine macrophages. Toxicol Sci. 2004;81(2):518–27.
Jayanthi S, Deng X, Noailles PA, Ladenheim B, Cadet JL. Methamphetamine induces neuronal apoptosis via cross-talks between endoplasmic reticulum and mitochondria-dependent death cascades. FASEB J. 2004;18(2):238–51.
Duronio V. The life of a cell: apoptosis regulation by the PI3K/PKB pathway. Biochem J. 2008;415(3):333–44.
Song L, De Sarno P, Jope RS. Central role of glycogen synthase kinase-3beta in endoplasmic reticulum stress-induced caspase-3 activation. J Biol Chem. 2002;277(47):44701–8.
Vene R, Larghero P, Arena G, Sporn MB, Albini A, Tosetti F. Glycogen synthase kinase 3beta regulates cell death induced by synthetic triterpenoids. Cancer Res. 2008;68(17):6987–96.
Brama M, Gnessi L, Basciani S, Cerulli N, Politi L, Spera G, et al. Cadmium induces mitogenic signaling in breast cancer cell by an ERalpha-dependent mechanism. Mol Cell Endocrinol. 2007;264(1–2):102–8.
Kim SM, Park JG, Baek WK, Suh MH, Lee H, Yoo SK, et al. Cadmium specifically induces MKP-1 expression via the glutathione depletion-mediated p38 MAPK activation in C6 glioma cells. Neurosci Lett. 2008;440(3):289–93.
Misra UK, Gawdi G, Pizzo SV. Induction of mitogenic signalling in the 1LN prostate cell line on exposure to submicromolar concentrations of cadmium+. Cell Signal. 2003;15(11):1059–70.
Ougolkov AV, Bone ND, Fernandez-Zapico ME, Kay NE, Billadeau DD. Inhibition of glycogen synthase kinase-3 activity leads to epigenetic silencing of nuclear factor kappaB target genes and induction of apoptosis in chronic lymphocytic leukemia B cells. Blood. 2007;110:735–42.
Maurer U, Preiss F, Brauns-Schubert P, Schlicher L, Celine C. GSK-3- at the crossroads of cell death and survival. J Cell Sci. 2014;127:1369–78.
Oyadomari S, Mori M. Roles of CHOP/GADD153 in endoplasmic reticulum stress. Cell Death Differ. 2004;11(4):381–9.
We would like thank Dr. Sun Don Kim for his suggestion on the study.
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Kim, S., Cheon, H., Kim, S. et al. GSK-3β-mediated regulation of cadmium-induced cell death and survival. Cell Mol Biol Lett 23, 9 (2018). https://doi.org/10.1186/s11658-018-0076-2