- Open Access
Valproate pretreatment protects pancreatic β-cells from palmitate-induced ER stress and apoptosis by inhibiting glycogen synthase kinase-3β
© Huang et al.; licensee BioMed Central Ltd. 2014
- Received: 1 February 2014
- Accepted: 29 April 2014
- Published: 4 May 2014
Reduction of pancreatic β-cells mass, major secondary to increased β-cells apoptosis, is increasingly recognized as one of the main contributing factors to the pathogenesis of type 2 diabetes (T2D), and saturated free fatty acid palmitate has been shown to induce endoplasmic reticulum (ER) stress that may contribute to promoting β-cells apoptosis. Recent literature suggests that valproate, a diffusely prescribed drug in the treatment of epilepsy and bipolar disorder, can inhibit glycogen synthase kinase-3β (GSK-3β) activity and has cytoprotective effects in neuronal cells and HepG2 cells. Thus, we hypothesized that valproate may protect INS-1 β-cells from palmitate-induced apoptosis via inhibiting GSK-3β.
Valproate pretreatment remarkable prevented palmitate-mediated cytotoxicity and apoptosis (lipotoxicity) as well as ER distension. Furthermore, palmitate triggered ER stress as evidenced by increased mRNA levels of C/EBP homologous protein (CHOP) and activating transcription factor 4 (ATF4) in a time-dependent fashion. However, valproate not only reduced the mRNA and protein expression of CHOP but also inhibited GSK-3β and caspase-3 activity induced by palmitate, whereas, the mRNA expression of ATF4 was not affected. Interestingly, TDZD-8, a specific GSK-3β inhibitor, also showed the similar effect on lipotoxicity and ER stress as valproate in INS-1 cells. Finally, compared with CHOP knockdown, valproate displayed better cytoprotection against palmitate.
Valproate may protect β-cells from palmitate-induced apoptosis and ER stress via GSK-3β inhibition, independent of ATF4/CHOP pathway. Besides, GSK-3β, rather than CHOP, may be a more promising therapeutic target for T2D.
- Endoplasmic reticulum stress
- Glycogen synthase kinase-3β
- Pancreatic β-cells
Type 2 diabetes (T2D) is a major cause of morbidity and mortality, decreasing both the quality of life and life expectancy. Modern lifestyles, characterized by the over consumption of high-calorie and high-fat food which is rich in the saturated free fatty acid palmitate (C16 : 0) and reduced physical activity, have dramatically boosted the rate of T2D[1–3]. Insulin resistance has long been regarded as a central factor for its development. Recently, reduction of β-cells mass, mainly due to increased apoptosis, is increasingly recognized as one of the key contributing factors to the pathogenesis of T2D[4, 5]. However, the precise mechanisms of β-cells apoptosis are not well established.
The endoplasmic reticulum (ER) is a highly dynamic organelle with a central role in lipid and protein biosynthesis and Ca2+ storage. Knowing the importance of ER for normal cellular function, the maintenance of ER homeostasis is essential to cell survival. Loss of homeostasis activates an adaptive response, which is called unfolded protein response (UPR), also known as ER stress. However, if homeostasis fails to be restored, the ER stress would initiate apoptosis pathways. β-cells, due to their heavy engagement in insulin secretion, have been found to be very sensitive to disruptions in ER homeostasis[7, 8], and accumulating evidence suggests that saturated free fatty acids (FFAs), such as palmitate, have been shown to trigger ER stress that may contribute to promoting β-cells apoptosis.
Glycogen synthase kinase-3β (GSK-3β), a multifunctional serine/threonine protein kinase, is considered as a negative regulator of β-cells mass[10, 11]. Mice with conditional ablation of GSK-3β in β-cells results in expansion of β-cells mass accompanied by enhanced proliferation and decreased apoptosis by promoting the insulin receptor/phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathway. But, the explicit mechanisms that GSK-3β promotes β-cells apoptosis have not been clearly clarified. Several groups have identified the obligatory role of GSK-3β in ER stress-induced apoptosis in HepG2 cells and a variety of neuronal cells[12–14]. While, whether GSK-3β also plays a central role in ER stress-induced β-cells apoptosis has not been exactly verified.
Valproate (VPA), the most widely used anticonvulsant and mood-stabilizing drug like lithium, has been demonstrated to have neuroprotective effects in neurodegenerative conditions[16–18]. Although the mechanisms of action of this drug have not been yet elucidated, several candidate pathways have been implicated, including direct inhibition of histone deacetylases (HDAC) and GSK-3β inhibition[18, 20].
In the present study, we hypothesized that valproate may protect β-cells from palmitate-induced apoptosis via inhibiting GSK-3β.
Rat INS-1 pancreatic β-cells were obtained from the China Center for Type Culture Collection and cultured as previously described.
Palmitate (Sigma-Aldrich, St Louis, MO) was added to the INS-1 cells by conjugating palmitate with fatty acid-free bovine serum albumin (BSA), and the stock solution of palmitate was prepared as described previously. Briefly, A 5 mM palmitate/5% BSA (5 mM PA) stock solution was prepared by mixing 1 ml 100 mM palmitate with 19 ml 5.26% BSA in a 55°C water bath. During experiment, 5 mM PA was diluted in RPMI 1640 without fetal bovine serum (FBS) to desired concentrations (palmitate: BSA: molar ratio of 6.6:1).
Cell viability assay
Cell viability was measured with cell counting kit-8 (CCK-8; Beyotime, Jiangsu, China) following the manufacturer’s instructions. The percentage of cell viability was calculated as follows: cell viability (%) = (OD of treatment - OD of blank control)/(OD of control - OD of blank control) × 100.
Hoechst 33342 and propidium iodide (PI) staining
For qualitative analysis of apoptosis, the cells were washed twice with PBS and then incubated with 10 μg/ml of Hoechst 33342 (Sigma-Aldrich, St Louis, MO) for 10 min at 37°C, following incubation with 10 μg/ml of PI (Sigma-Aldrich, St Louis, MO) for 15 min at room temperature. Images were collected on a fluorescence microscopy at 400 × magnification (Olympus, Tokyo, Japan).
Quantitative analysis of apoptosis was evaluated by flow cytometry with Alexa Fluor® 647 Annexin V (Annexin V; Biolegend, San Diego, CA ) and PI double staining according to the guidelines. A total of 15,000 events were collected and analyzed by flow cytometry (BD, San Diego, USA). Cells that bound Annexin V but excluded PI were considered apoptotic, and cells permeant to PI were deemed necrotic.
Transmission electron microscopy
The morphology of ER and apoptosis were assessed by transmission electron microscope (TEM) as described previously. Images were collected with a FEI Tecnai G2 12 TEM (FEI Company, Eindhoven, Netherlands).
Real-time quantitative PCR
Total RNA was extracted from cultured cells with Trizol reagent (Invitrogen) following the guidelines. Real-time quantitative PCR (RT-PCR) was performed as previously described. Primer sequences used to amplify rat activating transcription factor 4 (ATF4) and C/EBP homologous protein (CHOP) were as follows: ATF4, 5′-GAGCTTCCTGAACAGCGAAGTG-3′ (forward), and 5′-TGGCCACCTCCAGATAGTCATC-3′ (reverse); CHOP, 5′-TGGAAGCCTGGTATGAGGATCTG-3′ (forward), and 5′-GAGGTGCTTGTGACCTCTGCTG-3′ (reverse); GAPDH, 5′-GGCACAGTCAAGGCTGAGAATG-3′ (forward) and 5′-ATGGTGGTGAAGACGCCAGTA-3′ (reverse). Relative gene expression was calculated according to the comparative threshold cycle (2−∆∆Ct) method.
Western blot analysis
Cell proteins were extracted in radioimmunoprecipitation assay (RIPA) lysis buffer containing phenylmethyl sulfonylfluoride, and protein concentrations were determined by the BCA protein assay kit (Beyotime, Jiangsu, China), according to the manufacturer’s instructions. Western blot was performed as previously described. The following antibodies were used: CHOP, GSK-3β, phospho-GSK-3β (Ser9), caspase-3 (Cell Signaling Technology, Danvers, MA; 1: 1,000) and GAPDH (Santa Cruz Biotechnology; 1: 2,000).
Small interfering RNA transfection
CHOP knockdown was performed using small interfering RNA (siRNA) in INS-1 cells. Two siRNA duplexes targeting encoding regions of rat CHOP and one cy3-labeled scrambled siRNA (Mock) were designed and chemically synthesized (Ribobio, Canton, China). The oligonucleotide sequences were as follows: siCHOP-1 (targeting sequence: GGCTCAAGCAGGAAATCGA), 5′-GGCUCAAGCAGGAAAUCGAdTdT-3′ (forward), and 3′-dTdTCCGAGUUCGUCCUUUAGCU-5′ (reverse); siCHOP-2 (targeting sequence: CCAGATTCCAGTCAGAGTT), 5′-CCAGAUUCCAGUCAGAGUUdTdT-3′ (forward), and 3′-dTdTGGUCUAAGGUCAGUCUCAA-5′ (reverse).
INS-1 cells were transfected with the two CHOP siRNAs or scrambled siRNA using Lipofectamine RNAiMAX reagent (Invitrogen, Carlsbad, CA) following the manufacturer’s instructions. A final 50 nM siRNA was added to INS-1 cells for 48 h, then the efficiency of silence was assessed by RT-PCR and Western blot.
All data are presented as mean ± SD. Statistical significance between two conditions was analyzed by the independent-sample t-test and between three or more groups using one-way ANOVA, where P < 0.05 was considered statistically significant.
Palmitate reduces INS-1 cells survival in a time-concentration dependent fashion, primarily due to increased β-cells apoptosis
Valproate pretreatment prevents palmitate-induced cytotoxicity
Valproate pretreatment protects INS-1 cells from palmitate-induced apoptosis and ER distension
Then we observed the morphology of ER and apoptosis by electron microscopy. Palmitate-treated cells exhibited marked chromatin condensation, an indication of apoptosis. Meanwhile, we observed electron-lucent clefts extending throughout the cytoplasm which were continuous with abnormal nuclear envelope, suggesting that ER appears distended in the process of palmitate-induced INS-1 cells apoptosis. As expected, we rarely observed apoptosis and dilated ER in valproate pretreatment group (Figure 3C). These findings are consistent with our previous results and further support the hypothesis that valproate treatment increases the resistance of INS-1 cells to palmitate-induced apoptosis as well as ER distension.
Valproate ameliorates palmitate-induced caspase-3 dependent apoptosis by GSK-3β inhibition
To confirm the cytoprotection of GSK-3β inhibition, we examined the influence of two other GSK-3β inhibitors, LiCl and TDZD-8, on palmitate-induced cytotoxicity. 2 mM LiCl and 10 μM TDZD-8 had no cytotoxic effect on INS-1 cells (Additional file1: Figure S1). 10 μM TDZD-8, similar with valproate, had a strong cytoprotective effect against palmitate-induced toxicity at different time points (P < 0.001). Unexpectedly, 2 mM LiCl partially protected against palmitate-induced cytotoxicity after 24 h (P < 0.001), but not after 36 or 48 h (Figure 4B).
Valproate prevents palmitate-induced ER stress, independent of ATF4/CHOP pathway
Next, we focused on whether valproate could decrease palmitate-induced CHOP protein expression and found that valproate pretreatment weakened palmitate-induced CHOP protein level (P < 0.05; Figure 5D). These findings suggest that valproate blocks palmitate-induced ER stress by reducing CHOP expression, independent of ATF4/CHOP pathway.
Valproate pretreatment, rather than CHOP knockdown, prevents palmitate-induced INS-1 cells lipotoxicity
50 nM CHOP siRNAs has no cytotoxic effect on INS-1 cells, and our results showed that CHOP siRNAs protected against palmitate-induced cytotoxicity after 24 h (P < 0.05), but not after 48 h treatment (Figure 6C), indicating that CHOP knockdown delays, but does not prevent palmitate-induced cytotoxicity. Finally, we compared the cytoprotection of CHOP siRNAs with valproate by flow cytometry, and agreed with CCK-8 assay, only valproate but not CHOP siRNAs protected INS-1 cells from palmitate-induced apoptosis after 48 h treatment (P < 0.01, Figure 6D).
Strong evidence indicates that the global epidemic of T2D is tied to escalating rates of obesity in adults as well as in youths, and obesity, associated with elevated levels of circulating FFAs, is a major risk factor for the development of T2D. Palmitate is one of the most abundant dietary saturated FFAs, which are reflected in plasma and tissue lipids, furthermore, several studies have demonstrated that saturated FFAs such as palmitate induce β-cells apoptosis, which is increasingly recognized as one of the main influence factors to the pathogenesis of T2D[4, 5, 9, 22]. Our study confirmed that treatment with 0.25-1.0 mM palmitate for 6–48 h reduced INS-1 cells survival in a time-concentration dependent manner, largely due to enhanced β-cells apoptosis.
GSK-3β is considered as a promoter of β-cells apoptosis, but the explicit mechanisms that GSK-3β promotes β-cells apoptosis have not been clearly elucidated. Several groups have identified that GSK-3β is involved in ER stress-induced apoptosis in a variety of cells, including neuronal cells, HepG2 cells and mouse insulinoma (MIN6) cells[12–15]. Furthermore, valproate has been identified to protect HepG2 cells from tunicamycin or A23187 induced apoptosis partly mediated by directly inhibiting GSK-3β. In the present study, we examined whether valproate protects β-cells from palmitate-induced apoptosis via GSK-3β inhibition.
Our results showed that only valproate pretreatment revealed a strong cytoprotective effect against palmitate-induced toxicity. According to the reported findings, the possible reason that the cytoprotection of valproate requires extended pretreatment is that the effect of valproate has time dependency in a certain time. In addition, we found that valproate pretreatment, at clinically relevant doses, protected INS-1 cells from palmitate-induced apoptosis as well as ER distension, which may be an indicator of ER stress. Meanwhile, co-treatment with valproate and palmitate significantly decreased palmitate-induced caspase-3 activation as well as GSK-3β activation. Our results suggest that GSK-3β is involved in palmitate-induced caspase-3 dependent apoptosis in INS-1 cells, whereas valproate may protect INS-1 cells from palmitate-induced apoptosis via GSK-3β inhibition.
If valproate could protect INS-1 cells from palmitate-induced dysfunction by virtue of its ability to inhibit GSK-3β, then other inhibitors of GSK-3β should confer similar protection. As expected, TDZD-8, a specific GSK-3β inhibitor, also showed prominent cytoprotective effect against palmitate-induced cytotoxicity. Whereas, LiCl only partially protected against palmitate-induced cytotoxic effect in INS-1 cells. This result is somewhat different from several reported findings that 10 or 20 mM LiCl have cytoprotective properties against an array of insults in neuroblastoma cells and preadipocytes[31, 32]. Although the cytoprotection of LiCl and valproate varies between cell types and cellular stresses. The other possible reason is that the ability of GSK-3β inhibition of LiCl has concentration dependency. Because LiCl has cytotoxic effect on INS-1 cells at a lower concentration, and apparent toxicity was observed at concentrations over 10 mM. We performed the pretreatment with 2 mM LiCl, while 2 mM LiCl may not be effective to inhibit GSK-3β in INS-1 cells. Furthermore, compared with LiCl, valproate is a more effective inhibitor of GSK-3β. Together these results suggest that GSK-3β plays a critical role in palmitate-induced β-cells apoptosis, furthermore, GSK-3β inhibition could be one of the main mechanisms that valproate prevents palmitate-induced apoptosis in INS-1 cells. However, according to the present study, we cannot exclude the possibility that HDAC inhibition or other effects contribute to the observed cytoprotective effect of valproate.
ER stress is a double-edged sword. When homeostasis is disturbed, ER stress has three master transducers which serve to mitigate stress: inositol requiring enzyme 1 (IRE1), activating transcription factor 6 (ATF6), and PKR-like ER kinase (PERK). In PERK branch, the persistent phosphorylation of eukaryotic translation initiation factor 2α (eIF2α) by PERK increases CHOP expression via ATF4. However, if homeostasis fails to be maintained, the ER stress would trigger apoptosis. To date, several proteins involved in ER stress-induced apoptosis have been identified, including CHOP, c-Jun NH2-terminal kinase (JNK), and caspase-12. Furthermore, proapoptotic marker CHOP plays an important role in palmitate-induced β-cells apoptosis, which is mainly dependent on PERK pathway[9, 34, 35].
Although some groups have identified the obligatory role of GSK-3β in ER stress-induced apoptosis, the effects of GSK-3β on ER stress are inconsistent. In neuronal cells, the GSK-3β inhibitor LiCl strongly attenuates CHOP expression induced by ER stress agent tunicamycin treatment, but the mechanism by which GSK-3β regulates CHOP expression does not involve regulation of the two most prominent transcription factors that can induce CHOP, ATF4 and ATF6, while in HepG2 cells and MIN6 cells, down-regulation of GSK-3β prevents cells from ER stress-induced apoptosis without altering the level of ER stress proapoptotic marker CHOP[13, 15].
In the current study, we confirmed that ER stress contributed to palmitate-induced caspase-3 dependent apoptosis in INS-1 cells. The PERK pathway was activated as evidence that the mRNA expressions of ATF4 and CHOP were significant up-regulated by palmitate in a time-concentration dependent manner. Interestingly, compared with palmitate-treated group, pretreatment with either valproate or TDZD-8 before challenge with palmitate significantly decreased CHOP level, whereas, the expression of ATF4 was not affected. Our results suggest that valproate and TDZD-8 prevent palmitate-induced ER stress by reducing CHOP expression, independent of ATF4/CHOP pathway.
In addition, according to our results, we speculated that GSK-3β is upstream of ER stress-induced CHOP expression in INS-1 cells. Though GSK-3β may promote palmitate-induced ER stress via CHOP, up-regulation of CHOP expression cannot be the only mechanism that GSK-3β promotes the apoptosis during palmitate treatment, because CHOP knockdown delayed, but did not prevent palmitate-induced cytotoxicity. Furthermore, compared with CHOP knockdown, valproate displayed better cytoprotection against palmitate. Thus, we deduced that GSK-3β rather than CHOP may be a more efficient target to prevent palmitate-induced apoptosis. Nevertheless, how GSK-3β facilitates apoptosis remains unclear, several candidate pathways have been involved, including p53, pancreas/duodenum homeobox protein-1 (PDX-1), heat shock factor-1 (HSF-1), eukaryotic initiation factor 2B (eIF2B) and cyclic AMP response element-binding protein (CREB)[10, 36–38].
In summary, our work suggests that both GSK-3β and ER stress are involved in palmitate-induced caspase-3 dependent apoptosis in INS-1 cells. Valproate, at clinically relevant doses, may protect β-cells from palmitate-induced apoptosis and ER stress via GSK-3β inhibition, independent of ATF4/CHOP pathway. Besides, GSK-3β, rather than CHOP, may be a more promising therapeutic target for T2D. Further studies will be required in different types of β-cells and in animal models to explore the potential efficacy of GSK-3β on β-cells apoptosis and the explicit mechanisms that GSK-3β promotes β-cells apoptosis.
This work was supported by a research grant from the 12th Five-year Plan National Key Technology R&D Program (2012BAI09B04), Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT1131), and a Health Section Fund from the Ministry of Health of China (201002006).
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