Mycophenolic acid (MPA) is one of many effective immunosuppressive drugs. However, MPA can induce cellular toxicity and impair cellular function in β-cells. To explore the effects of MPA and the relation between MPA and Trx-1, we used various methods, including an Illumina microarray, to identify the genes regulated during pancreatic β-cell death following MPA treatment. INS-1E cells (a pancreatic β-cell line) and isolated rat islets were treated with MPA for 12, 24, or 36 h, and subsequent microarray analysis showed that (Trx1) gene expression was significantly reduced by MPA. Further, Trx1 overexpression increased the cell viability, decreased the activations of c-jun N-terminal kinase (JNK) and caspase-3 by MPA, and attenuated ROS upregulation by MPA. Furthermore, siRNA knockdown of Trx1 increased MPA-induced cell death and the activations of p-JNK and caspase-3, and MPA significantly provoked the apoptosis of insulin-secreting cells via Trx1 downregulation. Our findings suggest that the prevention of Trx1 downregulation in response to MPA is critical for successful islet transplantation.
Mycophenolic acid (MPA) is a potent, noncompetitive, reversible inhibitor of inosine-5′-monophosphate dehydrogenase (IMPDH), a key enzyme in the purine de novo synthetic pathway of guanosine nucleotides,1, 2 and is widely used to prevent rejection after solid organ or islet transplantation.3, 4 MPA effectively induces cell-cycle arrest in the late G1 phase in lymphocytes and more potently inhibits lymphocyte proliferation than the proliferations of other cell types.1, 5, 6 However, prolonged guanosine triphosphate (GTP) depletion induces the apoptosis of insulin-secreting cells.6, 7, 8 Recently, it was suggested that MPA-mediated GTP depletion blocks DNA synthesis and induces β-cell death,6, 7, 9, 10 but the mechanism responsible for MPA-induced β-cell death was not determined. We previously reported the specific depletion of GTP via the MPA-induced apoptosis of insulin-secreting cells (HIT-T15, RIN-5, INS-1E, and isolated rat islets) and also confirmed that co-treatment with GTP completely blocked MPA-induced cell death, which suggest that MPA inhibits de novo GTP synthesis and depletes GTP.11, 12, 13 In addition, we identified genes expressionally altered during MPA-induced β-cell death and grouped these genes by cellular function. In particular, the expressions of 386 genes in INS-1E cells and of 234 genes in primary rat islet cells were found to be significantly altered by MPA as determined using an Illumina cDNA microarray.13 Further, the expressions of some genes, such as, RhoGDI-α, Thioredoxin 1 (Trx1), Bcl2-related protein, and programmed cell death 2 (pdcd 2), are known to be closely related to MPA-induced β-cell death.13, 14, 15
Trxs are small (∼12 kDa) proteins that are found in several types of cells. These proteins operate in combination with Trx reductase and nicotinamide adenine dinucleotide phosphate (NADPH) as protein disulfide/dithiol reducing systems.16, 17 In mammals, three members of the Trx family have been identified, namely, Trx1, Trx2 (the mitochondrially localized form), and Sptrx (sperm Trx, also designated p32TrxL).18, 19 Trx1 is a multifunctional protein that is present in the extracellular milieu, cytoplasm, and nucleus, and has distinct roles in these environments.20 The cellular activity of Trx1 is regulated by its total expression, localization (nucleus or cytosol) and protein–protein interactions, and by posttranslational modification.21 In the extracellular environment, Trx1 exhibits chemokine-like activity,22 whereas in the cytoplasm, by scavenging reactive oxygen species (ROS) and activating transcriptional factors, Trx1 is involved in a wide range of cellular responses, such as cell proliferation, apoptosis, and protection.23, 24, 25, 26 The harmful effects of oxidative stress are considered to be especially relevant for β-cells because they express only low levels of antioxidant enzymes, such as superoxide dismutase (SOD, which converts superoxide radicals to H2O2), catalase, cellular glutathione peroxidase (Gpx-1, which detoxifies H2O2), and Trx.27, 28 Further, the preventions of autoimmune and STZ-induced diabetes by Trx1 overexpression in β-cells suggest that Trx1 has important effects on β-cell destruction in type 1 diabetes (T1D) and on genetic susceptibility to T1D,27, 29 and indicate that Trx1 has a critical role during β-cell death in T1D.
The objective of this study was to investigate the apoptotic effect of MPA on insulin-producing cells and to examine the role of Trx1 in this process. To explore these effects of MPA, we used various methods, including an Illumina microarray, to identify those genes regulated during pancreatic β-cell death following MPA treatment. In order to identify the effects of Trx1 downregulation on MPA-induced apoptosis, we observed the effects of Trx1 overexpression and knockdown on MPA treatment in rat INS-1E cells (an insulin-producing cell line). In addition, we examined the relationship between Trx1 expression and ROS generation during MPA-induced apoptosis in INS-1E cells.
The identification of genes modulated by MPA using a microarray
Previously, we reported differentially expressed gene profiles during MPA-induced β-cell death.13 For this analysis, INS-1E cells and isolated primary islets from rats were treated with 40 μM MPA for 24 h or 48 h. INS-1E cells and isolated islets were analyzed using an Illumina RatRef-12 Expression BeadChip. Previous analysis identified genes related to the apoptosis signaling pathway and showed that decreased RhoGDI-α to Rac1 binding increased Rac1 activity.13, 30 Accumulating evidence indicates that Rac1 has a negative modulatory effect on the metabolic dysfunction of islet β-cells, especially with respect to the regulation of Nox activation.31 Further, recent studies have implicated Nox in the constitutive generation of ROS following the long-term exposure of β-cells to various stimuli known to cause metabolic dysregulation.32, 33, 34 In the present study, we grouped genes by molecular function and then focused on the oxidoreductase group, which accounted for many differentially expressed genes. It was found that 19 genes belonging to the oxidoreductase group were expressed at high values (>±twofold versus control cells) (P<0.05, n=4). In particular, this analysis confirmed that Trx1 gene expression was decreased by MPA (Table 1). These findings suggest that the downregulation of Trx1 by MPA in INS-1E cells is associated with MPA-induced β-cell apoptosis.
Changes in Trx1 expression during MPA-induced apoptosis
To confirm our microarray results, quantitative real-time PCR (qPCR) was performed after treating INS-1E cells with 10 μM MPA for 12, 24, or 36 h. In order to rescue GTP depletion after MPA treatment, 100 μM of GTP was co-treated into INS-1E cell for 36 h. Real-time PCR showed that mRNA expression levels decreased to 0.66±0.03 at 12 h, 0.43±0.09 at 24 h, and to 0.20±0.10 at 36 h versus the untreated control (CTL) (Figure 1a). Further, the gene expression level of Trx1 was time-dependently reduced by MPA. However, co-treatment with 10 μM MPA plus 100 μM GTP effectively prevented loss of Trx1 expression at 36 h (0.60±0.01). These results were in line with our Genechip results. To quantify Trx1 protein expression under the same experimental conditions, we immunoblotted total protein lysates. The protein expression of Trx1 was found to decrease in INS-1E cells during MPA-induced cell death, but co-treatment with GTP significantly prevented this Trx1 protein deletion (Figure 1b).
Primary rat islet cells correspond more closely than INS-1E cells to therapeutic islet transplants, and hence we evaluated the effects of MPA on rat islet cells and compared the mechanism of MPA-induced cell death in these primary cultures with that in the INS-1E cell line. Real-time PCR was performed after treating islet cells with 40 μM MPA for 12 h, 24 h, or 36 h and after co-treating them with 40 μM MPA plus 100 uM GTP for 36 h. As is shown in Figure 1a, mRNA expression levels decreased to 0.89±0.01 at 12 h, 0.66±0.03 at 24 h, and to 0.63±0.02 at 36 h versus the untreated control (CTL) (Figure 1c). Further, although Trx1 mRNA decreased time-dependently after MPA treatment, co-treatment with MPA plus GTP maintained Trx1 mRNA expression at a higher level (0.92±0.06 at 36 h) than treatment with MPA alone. In addition, treatment with MPA decreased Trx1 protein expression in primary islet cells, but co-treatment with MPA plus GTP suppressed this response (Figure 1d).
Using immunohistochemistry, we confirmed that Trx1 protein expression was downregulated during apoptosis in primary rat islets treated with 40 μM MPA. To identify β-cells, islet cluster sections were stained for insulin. It is known that the cytoarchitectures of pancreatic islets are species dependent. In particular, rodent islets are characterized by a predominance of insulin-producing β-cells in the cores of islet clusters and by scarce alpha, delta, and PP cells in peripheries.35, 36 As shown in Figure 2, Trx1 (red) expression level in β-cells (colored green; especially in islet cores) decreased over time after treatment with 40 μM MPA for 12, 24, or 36 h. Quantitative analysis of Trx1/insulin staining ratios showed reduced Trx1 expression in the β-cells of isolated rat islets. The number of Trx1 and insulin positive cells reduced with MPA treatment time, and the protein expression of Trx1 was especially reduced in β-cells. However, co-treatment with 40 μM MPA plus 100 μM GTP increased the number of β-cells expressing Trx1 protein. Consequentially, Trx1 expressions in β-cells (isolated rat islets) decreased after MPA treatment. These results agree with the results obtained using the INS-1E cell line and show that reduced Trx1 expression is linked to β-cell toxicity in response to MPA.
Effects of Trx1 expression on INS-1E cell survival during MPA-induced apoptosis
To investigate the effects of Trx1 expression on the survival of INS-1E cells, we established INS-1E cells stably expressing Trx1 from pcDNA 3.1 and transiently transfected these cells with Trx1 siRNA (Figure 3a). As shown in Figure 3b, although Trx1 overexpression reduced MPA-induced cell death versus the control (transfected with vector only), Trx1 knockdown increased cell death. More specifically, the viability of INS-1E cells decreased to 72±3.2% versus control cells after treatment with 10 μM MPA for 24 h, but the viability of Trx1-overexpressing cells was similar to that of the control (98.5±0.5% of control at 24 h). These results suggest that Trx1 is involved in MPA-induced β-cell apoptosis.
Changes in Trx1 expression were closely associated with MAPK-dependent apoptosis
In earlier studies, we found that MPA induced apoptosis in several pancreatic β-cell lines via JNK activation,12, 13, 37 and thus we investigated the effect of Trx1 expression on the MAPK signaling pathway. After treating INS-1E cells and the Trx1-overexpressing INS-1E cell line with 10 μM MPA for 12 h, 24 h, or 36 h, p-MKK4/7, p-JNK, and cleaved caspase-3 protein levels were measured by western blotting. p-MKK4/7 was observed at 12 h and its level was increased at 24 h. However, this increase was not observed at any time in Trx1-overexpressing cells (Figure 4a). p-JNK protein levels were dramatically increased at 24 h and slightly more increased at 36 h versus untreated controls, but its levels were increased only at 36 h in Trx1-overexpressing cells (Figure 4b). The expression of cleaved caspase-3 was markedly lower in Trx1-overexpressing cells than in INS-1E cells (Figure 4c). Further, Trx1 knockdown increased the activations of MKK4/7, JNK, and caspase-3 (Supplementary data 1). These results show that Trx1 expression regulates MPA-induced apoptosis via an MAPK-dependent signaling pathway.
ROS level measurements in INS-1E cells treated with MPA
The key biological activities of Trx1 include antioxidative, antiapoptotic, and growth-stimulatory effects, which are attributable to its interactions with nuclear factor-κB (NF-κB), apoptosis signal regulating kinase-1 (ASK-1), and hypoxia-inducible factor-1.24, 37, 38 The most distinctive role of Trx1 concerns the repair of proteins oxidized by reactive oxygen-containing intermediates. Therefore, we used DCF-DA to detect cellular ROS in INS-1E cells treated with MPA. Cellular ROS generation was observed by fluorescence microscopy after treating INS-1E and Trx1-overexpressing INS-1E cells with 10 μM MPA. As shown in Figure 5a, cellular ROS increased during MPA-induced apoptosis, whereas ROS generation was obviously less in Trx1-overexpressing cells. To quantify intracellular ROS levels more precisely, we used fluorescence spectrophotometry. Intracellular ROS levels in INS-1E cells increased in a time-dependent manner after treatment with 10 μM MPA for 12 h, 24 h, or 36 h (by 104.3±0.9%, 118.3±9.8%, and 137.0±8.7% of the untreated control levels, respectively). However, ROS generation in Trx1-overexpressing cells remained at the untreated control level at all times (99.7±4.5%, 107.0±9.0%, and 110.3±4.3% of untreated controls, respectively) (Figure 5b). These results show that Trx1 overexpression blocked ROS generation during MPA-induced β-cell apoptosis.
Although islet transplantation is more widely accessible and reproducible than pancreatic transplantation, it presents several issues in the clinical setting. In particular, transplants are susceptible to drug-induced toxicity and might be physiologically inadequate. MPA-induced β-cell toxicity can also affect islet graft survival,6, 7 but the signal transduction mechanisms responsible for MPA-induced β-cell toxicity have not been elucidated. In the present study, we investigated the role of Trx1 in MPA-induced β-cell apoptosis. In particular, we examined (1) changes in Trx1 expression during MPA-induced apoptosis, (2) the effects of Trx1 overexpression and knockdown on the effects of MPA treatment in the rat insulin-producing cell line INS-1E, and (3) the relationship between Trx1 expression and ROS generation in INS-1E cells during MPA-induced apoptosis. This study has two major findings. First, it demonstrates that MPA reduces Trx1 expression at the protein and gene levels in INS-1E cells and in isolated rat islets. Second, it shows that cell viability is restored by Trx1 overexpression, therefore preventing MPA-induced apoptosis via the MAPK pathway and suppressing ROS generation in response to MPA. Using the microarray technique, we found that numerous genes could be involved in the death of insulin-secreting cells exposed to MPA. As described in the introduction, Trx1 is a candidate antiapoptotic gene in insulin-secreting cells13 and probably exerts its antiapoptotic effect on the ischemic-reperfused hearts via its antioxidant and ASK-1 inhibitory effects. Further, treatment with Trx1 before reperfusion markedly inhibits p38 MAPK activity.39 In addition to its activity as an oxidoreductase, recent in vitro studies have demonstrated that Trx1 directly interacts with and inhibits the activity of ASK-1, a mitogen-activated protein kinase that activates the proapoptotic kinases, MAPK, and JNK.24, 404142 In this study, we found that modulations of Trx1 expression affected β-cell viability and the MAPK pathway after MPA treatment. Together, our findings and those described above indicate that Trx1 is associated with MPA-induced apoptosis via the MAPK signaling pathway in insulin-secreting cells.
Hotta et al.27 showed that Trx1 overexpression markedly reduced the incidence of diabetes but failed to prevent the development of insulitis. This result suggests that the autoimmune destruction of pancreatic β-cells in type 1 diabetes is at least partially mediated by reactive oxidative intermediates (ROIs) and that this mediation can be blocked by Trx1.28 In the islet transplantation experiment, Trx-overexpressed islets showed better glycemic control and longer graft survival, indicating that Trx has a strong cytoprotective effect on islets.29 These effects may reflect the multiple biological functions of Trx, which has both antioxidative and antiapoptotic activities. In the present study, Trx1 expression was inhibited by MPA, and the overexpression of Trx1 inhibited MPA-induced apoptosis by activating the JNK pathway, which suggests that pancreatic β-cell viability could be improved by Trx1 overexpression during MPA-induced apoptosis. In further studies, we suggest ASK-1 and TXNIP immunoassays be used to determine how MPA affects the expressions of these proteins, and that an additional study be undertaken to determine the nature of the relation between RhoGDI-α and Trx1, and the mechanism(s) responsible for regulating these genes.
Summarizing, we found MPA reduces the expression of Trx1 at the protein and gene levels, and that this downregulation leads to the apoptosis of insulin-secreting cells via the MKK4/7-JNK pathway. Further, our findings indicate Trx1 might mitigate MPA-induced islet cell death and indicate that further studies are needed to evaluate the effects of Trx1 modulation in transplant models.
Materials and Methods
Cells and culture reagents
Cells were maintained at 37 °C in a 5% CO2-humidified incubator. INS-1E insulinoma rat pancreatic β-cells were cultured in RPMI-1640 medium containing 10% fetal bovine serum (FBS) (Gibco, Grand Island, NY, USA), 100 units/ml penicillin, and 100 μg/ml streptomycin, and cells that overexpressed Trx1 were grown in RPMI-1640 medium containing 10% FBS and 0.2 mg/ml G418.
Islet isolation and primary cell culture
The pancreas of a Lewis rat (250–350 g) was digested using collagenase P (Roche, Indianapolis, IN, USA), and the islets so obtained were purified using three different Histopaque (Sigma Chemical Co., St Louis, MO, USA) gradients. Islets were maintained in RPMI-1640 medium containing 10% FBS (Gibco), 100 units/ml penicillin, and 100 μg/ml streptomycin in a humidified 5% CO2 atmosphere at 37 °C.
Illumina microarray gene analysis
Microarray analysis was performed using an Illumina RatRef-12 Expression BeadChip (Illumina, San Diego, CA, USA), according to the manufacturer's instructions (Macrogen, Seoul, Korea). Biotinylated cRNAs were prepared from 0.55 μg of total RNA using an Illumina Total Prep RNA Amplification Kit (Ambion, Austin, TX, USA). Following fragmentation, 0.75 μg of cRNA was hybridized to the Illumina RatRef-12 Expression BeadChip (Illumina). Arrays were scanned using an Illumina Bead Array Reader Confocal Scanner. Array data export processing and analysis were performed using Illumina BeadStudio v3.1.3 (Gene Expression Module v3.3.8, Stratagene, CA, USA).
Total RNA isolation
Following medium aspiration, INS-1E cells were lysed directly in culture dishes by adding TRIzol reagent (Invitrogen, Carlsbad, CA, USA). Lysed samples were incubated for 5 min at room temperature and then mixed with chloroform in a tube by vortexing for 15 s. Tubes were centrifuged at 12 000 × g for 15 min at 4 °C, and supernatants were transferred into new tubes containing isopropanol and then incubated at room temperature for 10 min. Samples were then centrifuged at 12 000 × g for 10 min at 4 °C. The supernatants obtained were discarded and pellets were washed in 70% ethanol and lysed in RNase-free water.
RT-PCR and quantitative real-time PCR
Total RNA was reverse transcribed using oligo-dT and a M-MLV Reverse Transcriptase (Invitrogen) protocol, and PCR was performed using Bioneer Accupower PCR PreMix (Bioneer, Korea). Real-time PCR was performed using cDNA, a TaqMan probe, and Real-time PCR master mix (QPK-101, TOYOBO, Osaka) using the Taqman assay protocol. Transcript values and Ct values were normalized against GAPDH and expressed as fold differences versus controls. The following Trx1 sequences were used: sense, 5′-IndexTermCTTTCATTCCCTCTGTGACAAGTATTC-3′, antisense, 5′-IndexTermTTATAGAACTGGAAGGTCGGCATG-3′, and the sequence of the Trx1 Taqman probe was 5′p-Fam-IndexTermCAGCAACATCCTGGCAGTCATCCACG-BHQ-1-3′F. The following GAPDH sequences were used: sense, 5′-IndexTermGTGATGCTGGTGCTGAGTATGTC-3′T, antisense 5′-IndexTermGCGGAAGGGGCGGAGATG-3′, and the sequence of the GAPDH Taqman probe was 5′a-Hex-IndexTermACCCTTCAGGTGAGCCCCAGCCTT-BHQ-1-3′H.
Western blot analysis
Protein extracts from the INS-1E cell line were prepared using RIPA buffer containing 50 mM Tris-HCl (pH 7.5), 150 mM NaCl, 1% Nonidet P-40, 0.5% sodium deoxycholic acid, and 0.1% SDS. Proteins were boiled for 5 min, separated by 10–15% SDS-PAGE, and blotted onto polyvinylidene difluoride membranes. Proteins were detected using the following primary antibodies: Trx1 (1 : 1000), cleaved caspase-3 (1 : 1000), p-Jun N-terminal kinase (JNK)/JNK (1 : 1000), p-MKK4/7 (1 : 1000) (Cell Signaling Technology, Beverly, MA, USA), and β-actin (1 : 10 000) (Sigma). Protein bands were detected using an Immobilon Western Chemiluminescent HRP substrate kit (Millipore Corporation, Billerica, MA, USA).
Primary isolated islets were treated with 40 μM MPA, fixed in 4% paraformaldehyde, and dehydrated using a 10, 20, and 30% sucrose series overnight. The sucrose solution was then removed from tubes, and ∼500 μl of Tissue Tek Optimal Cutting Temperature (OCT) solution (Thermo Fisher Scientific, Waltham, MA, USA) was added to islets. The OCT-embedded islets were stored at −80 °C. Sections (4-μm thick) were then cut on a cryostat, placed on silanized slides, and permeabilized and blocked with 0.5% BSA in PBS. Slides were incubated overnight at 4 °C with a primary polyclonal antibody against Trx1 (Cell Signaling) diluted 1 : 50 with blocking solution (0.5% BSA in PBS). Slides were then washed, incubated with an Alexa Fluor 568 goat anti-rabbit antibody (Invitrogen), and then with another primary polyclonal antibody against Insulin (Santa Cruz Biotechnology, Inc.) diluted 1 : 100. Slides were then washed and incubated with an Alexa Fluor 488 goat anti-mouse antibody (Invitrogen).
Fluorescence microscopic images of fixed cells were captured using an Olympus IX71 fluorescence microscope equipped with a DP71 camera and DP-BSW Application software (Olympus Corporation, Tokyo, Japan).
Trx1 gene cloning
In vitro Trx1 transcription templates were amplified by PCR from INS-1E cDNA using 5′-IndexTermTCCAATGTGGTGTTCCTTGA-3′ (forward) and 5′-IndexTermACCAGAGAACTCCCCAACCT-3′ (reverse). PCR products were cloned into mammalian and bacterial expression vectors using flanking restriction sites engineered into the PCR oligonucleotides. After subcloning cDNA into pcDNA 3.1 vector, the insert was fully sequenced using the dideoxy nucleotide chain termination method and Taq DNA polymerase. The vector was transfected into insulin-secreting cells over 2 h using 4 μl of Lipofectamine 2000 (Invitrogen) in 200 μl of serum-free culture medium.
INS-1E cells (1 × 106/well) cultured in six-well plates were transiently transfected with either small interfering RNAs (siRNAs) targeting Trx1 or scrambled negative control siRNAs. All siRNAs were purchased from QIAGEN Korea Ltd (Seoul, Korea). The following Trx1 sequences were used: sense, 5′-IndexTermGGGAGACAAGCUUGUGGUATT-3′ and antisense, 5′-IndexTermUACCACAAGCUUGUCUCCCGC-3′. Cells were transfected using Lipofectamine 2000 Reagent and Opti-MEM (Gibco) and analyzed by immunoblotting ∼24 h later.
Cell viability analysis
Cell viabilities were determined using an MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. Briefly, cells were seeded in a 24-well plate at a density of 2 × 105 cells/well and treated with 10 μM of MPA (Sigma) for 12 h, 24 h, or 36 h at 37 °C. MTT solution was added to each well to a final concentration of 1 mg/ml and incubated for 1 h at 37 °C. The formazan crystals formed were dissolved in Detergent Reagent (Trevigen, Gaithersburg, MD, USA), and absorbance at 540 nm was measured using an ELISA plate reader (Molecular Devices, Palo Alto, CA, USA).
Measurement of intracellular ROS production
The peroxide-sensitive fluorescent probe 2,7-dichlorodihydrofluorescein diacetate (DCF-DA; Molecular Probes, Carlsbad, CA, USA) was used to assess the generation of intracellular ROS. To observe intracellular ROS generation, treatment-naive INS-1E cells and cells overexpressing Trx1 were grown in six-well plates at a density of 7 × 105 cells/well, treated with 10, 40, or 80 μM of MPA for 12, 24, or 36 h, incubated at 37 °C for 30 min in the dark in serum-free medium containing 5 μM DCF-DA, and washed three times with phosphate-buffered saline (PBS). Fluorescence microscopic images were captured using an OlympusIX71 fluorescence microscope (Olympus Corporation). To quantify ROS levels, treatment-naive INS-1E cells and cells over-expressing Trx1 were grown in 96-well plates at a density of 4 × 104 cells/well, incubated with 10 μM DCF-DA at 37 °C for 30 min in the dark, and treated with 10μM MPA for 12, 24, or 36 h. Fluorescence was measured using a luminescence spectrophotometer (Perkin Elmer LS50B, Wellesley, USA) and at excitation and emission wavelengths of 485 and 530 nm, respectively. ROS levels were calculated as percentage increases versus untreated control levels.
Results are presented as means±SEMs. One-way ANOVA and the post hoc Student’s t-test were used to determine the significance of differences between means. Statistical significance was accepted for P-values of <0.05, and the analysis was conducted using GraphPad Prism software (GraphPad Software, Inc., CA, USA).
apoptosis signal-regulating kinase-1
Jun N-terminal kinase
nicotinamide adenine dinucleotide phosphate
programmed cell death 2
reactive oxidative intermediates
reactive oxygen species
small interfering RNA
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This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (2011-0023964).
The authors disclose the following relevant financial relationships: YC and JHD are research associates supported by Yonsei University IACF (7-2006-0253, 7-2012-0144); MSK has received grants from Novartis, Roche and Astellas; YSK has received grants from Astellas, Novartis, Wyeth, Pfizer, Roche, and CKD. The remaining authors declare no conflict of interest.
Edited by A Stephanou
KH Huh, Y-J Park, and YS Kim conceived and designed the experiments, Y Cho and JH Do performed the experiments, Y Cho, JH Do, KH Huh, and Y-J Park analyzed the data, and DJ Joo, KH Huh, MS Kim, and YS Kim contributed reagents, materials, or analysis tools. The paper was written by Y Cho, KH Huh, BS Kim, and YS Kim.
Supplementary Information accompanies this paper on Cell Death and Disease website
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