Endoplasmic reticulum stress associated apoptosis as a novel mechanism in indoxyl sulfate‑induced cardiomyocyte toxicity

Introduction

Cardiovascular disease remains the leading cause of morbidity and mortality in patients with chronic kidney disease (CKD), particularly in patients who elect to undergo dialysis treatment (1,2). Indoxyl sulfate (IS) is a typical protein-bound uremic toxin, which is challenging to remove using current dialysis techniques, and serves a central role in cardiac damage among patients with CKD (3). The authors' previous clinical research suggested that IS is associated with heart failure in patients undergoing hemodialysis (4). However, the mechanism underlying IS-induced cardiac tissue damage has yet to be fully revealed. Research has revealed that IS promotes cardiomyocyte hypertrophy and cardiac fibrosis via enhanced oxidative stress (5), and suppresses anti-oxidative mechanisms (6). Studies have also demonstrated that prolonged endoplasmic reticulum (ER) stress may serve an important role in cardiomyocyte hypertrophy and apoptosis (7–9). The ER is the cellular compartment in which proteins are synthesized and acquire the correct three-dimensional configuration needed for biological activity. When cells synthesize secretory proteins in quantities that exceed the capacity of the ER, unfolded proteins accumulate in the ER, inducing ER stress (ERS). In response to ERS, various ER chaperones, including glucose-regulated protein 78 (GRP78), are upregulated. When ERS is excessive and/or prolonged, the initiation of apoptosis is promoted by the transcriptional induction of CCAAT-enhancer-binding homologous protein (CHOP), and/or by the activation of c-Jun N-terminal kinase (JNK)-dependent pathways (10).

In the current study, the authors sought to examine whether IS causes cell apoptosis, and whether ERS participates in the molecular mechanism underlying IS-induced cardiac toxicity.

Materials and methods

Cells, culture and reagents

H9C2 cardiomyocytes (Type Culture Collection of the Chinese Academy of Sciences, Shanghai, China) were taken from liquid nitrogen and cultivated in Dulbecco's modified Eagle's medium (DMEM; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (Gibco; Thermo Fisher Scientific, Inc.), and maintained at 37°C in a humidified atmosphere containing 5% CO2. For different experiments, cells were seeded into 6-cm dishes or 6-well plates, or onto 12-mm-diameter glass coverslips in 24-well plates. IS and 4-phenylbutyric acid (4-PBA) were purchased from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany).

Experimental groups

To evaluate whether IS induces apoptosis in H9C2 cardiomyocytes, cells were exposed to increasing concentrations of IS (500, 1,000, and 2,000 µM) for 24 h, and apoptosis was detected by flow cytometry. To determine whether IS-induced apoptosis is associated with ERS, cells were divided into 4 groups: i) Control group (n=4): Cells were treated with serum-free DMEM for 48 h, culture medium was changed after the first 24 h; ii) PBA group (n=4): Cells were treated with PBA (1 mM) for 24 h, and then cultured with DMEM for 24 h; iii) IS group (n=4): Cells were treated with DMEM for 24 h, and then treated with IS (1 mM) for 24 h; and iv) PBA+IS group (n=4): Cells were pretreated with PBA (1 mM) for 24 h, prior to IS (1 mM) treatment for 24 h. Serum-free DMEM was used in all experimental groups. The present study determined 1 mM to be the optimal concentration of PBA, according to a previous study (11), and determined 1 mM to be the optimal concentration of IS with respect to its induction of apoptosis and ERS, which is presented in the results.

Flow cytometry

An apoptosis kit with Annexin-V Alexa Fluor™ 488 and propidium iodide (PI; Thermo Fisher Scientific, Inc.) was used to evaluate cell apoptosis. Cells were washed with cold PBS and binding buffer, and then stained with AnnexinV-FITC for 20 min at 4°C, followed by PI for 5 min per sample. Data were acquired using an Attune NxT Flow Cytometer (Thermo Fisher Scientific, Inc.), and FlowJo software (v.14.0; TreeStar, Inc. San Carlos, CA, USA) was used for data analysis.

Western blot assay

Protein samples from H9C2 cells were lysed in radio immunoprecipitation assay buffer (catalog no. KGP702, Keygen, Jiangsu, China). Lysates were centrifuged at 12,000 × g (4°C) for 5 min. Supernatants were collected, and equal amount of proteins (50 µg per sample) were subjected to 10% SDS-PAGE, followed by transference to Immobilon-PVDF membranes (Merck KGaA, Darmstadt, Germany) for 90 min at 110 V on ice. Membranes were incubated in 5% non-fat milk for 60 min at room temperature, and then reacted overnight at 4°C with specific antibodies: Anti-GRP78 (1:1,000, catalog no. 3183), anti-CHOP (1:1,000, catalog no. 2895), anti-phospho (p)-stress activated protein kinase (SAPK)/JNK (1:1,000, catalog no. 9255), anti-SAPK/JNK (1:1,000, catalog no. 9252), anti-cleaved-caspase 3 (1:1,000, catalog no. 9664) and anti-caspase3 (1:1,000, catalog no. 9662) were purchased from Cell Signaling Technology, Inc. Danvers, MA, USA. The membranes were rinsed in PBS 3 times (10 min each time), then incubated with the peroxidase-conjugated AffiniPure Goat anti-rabbit IgG antibody (1:10,000, catalog no. 111-035-003, Jackson ImmunoResearch Laboratories Inc., PA, USA) and peroxidase-conjugated AffiniPure Goat anti-mouse IgG antibody (1:10,000, catalog no. 115-035-003, Jackson ImmunoResearch Laboratories Inc., PA, USA) for 1 h at room temperature. Then, the membranes were rinsed 3 times (10 min each time) in PBS. Proteins were visualized by enhanced chemiluminescent reagents (Thermo Scientific, Inc.), and band intensity was analyzed using program Image-J software (v.1.4.3.67; National Center for Biotechnology Information).

Statistical analysis

All experiments were performed at least in triplicate. Data are presented as the mean ± standard deviation. Statistical differences were determined using analysis of variance coupled with Dunnett test or Tuckey's test. Statistical analysis was performed using SPSS software, version 22.0 (IBM SPSS, Armonk, NY, USA). P<0.05 was considered to indicate a statistically significant difference.

Results

IS stimulation induces apoptosis and ERS

Treatment of H9C2 cells was conducted using an IS concentration range of 0–2,000 µM, and cells were collected for apoptosis evaluation. IS (1,000–2,000 µM) significantly stimulated both early and late apoptosis (Fig. 1). Treatment of H9C2 cells occurred at IS concentrations ranging from 0–1,000 µM, and cells were collected for western blot analysis. Compared with the control group, the expression of the ER chaperone GRP78 was significantly increased in the IS 500 µΜ (P<0.05) and 1,000 µM (P<0.01) treated groups (Fig. 2). IS induced both apoptosis and ERS at a concentration of 1,000 µM. Therefore, 1,000 µM IS was used for subsequent experiments.

Figure 1. Determination of apoptosis in H9C2 cells. The apoptosis rate of H9C2 cells was measured following treatment with different concentrations of IS (n=4). ***P<0.001 vs. control group. IS, indoxyl sulfate; PI, propidium sulfide.

Figure 2. Protein expression level of GRP78. The protein expression level of endoplasmic reticulum chaperone GRP78 was determined in H9C2 cells following treatment with different concentrations of IS (n=4). *P<0.05, **P<0.01 vs. control group. IS, indoxyl sulfate; GRP78, glucose-regulated protein 78.

Apoptosis of H9C2 is associated with ERS in the context of IS stimulation

H9C2 cardiomyocytes were divided into 4 groups: i) Control group; ii) 4-PBA group; iii) IS group; and iv) 4-PBA+IS group. Compared with the control group, early apoptosis was significantly increased in the IS group (P<0.001), and early apoptosis was significantly attenuated in the 4-PBA+IS group, when compared with the IS group (P<0.001). A similar trend was observed with the late apoptosis phase, as presented in Fig. 3. Compared with the control group, the expression of cleaved-caspase-3 in the IS and 4-PBA+IS groups was significantly increased. Compared with IS group, the expression of cleaved-caspase-3 protein is significantly lower in 4-PBA+IS group (Fig. 4).

Figure 3. Determination of apoptosis in H9C2 cells under different treatment conditions. The apoptosis rate of H9C2 cardiomyocytes in groups 1 to 4 (control, 4-PBA, IS, and 4-PBA+IS) was determined (n=4). **P<0.01, ***P<0.001 IS, indoxyl sulfate; PI, propidium sulfide; 4-PBA, 4-phenylbutyric acid.

Figure 4. Protein expression levels of GRP78, CHOP, p-JNK and cleaved-caspase 3. The protein expression levels of GRP78, CHOP, p-JNK and cleaved-caspase 3 were determined in H9C2 cardiomyocytes in groups 1 to 4 (control, 4-PBA, IS, and 4-PBA+IS) (n=4). *P<0.05, **P<0.01, ***P<0.001. IS, indoxyl sulfate; 4-PBA, 4-phenylbutyric acid; GRP78, glucose-regulated protein 78; p, phosphorylated; CHOP, CCAAT-enhancer-binding protein homologous protein; JNK, c-Jun N-terminal kinase.

JNK-CHOP signaling pathway activity increases under IS stimulation

The protein expression levels of GRP78, CHOP and p-JNK in each group are presented in Fig. 4. Compared with the control group, the expression levels of GRP78 and CHOP in the IS and 4-PBA+IS groups were significantly increased, whereas the phosphorylation of JNK was only increased in the IS group. Compared with the IS group, the protein expression levels of GRP78 and CHOP were significantly decreased in the 4-PBA+IS group, as was the phosphorylation of JNK. No statistically significant difference was observed in the expression of these proteins between the control and the 4-PBA groups.

Discussion

The mechanisms of cardiovascular disease in hemodialysis patients are complex. Conventional risk factors, such as hypertension and volume overload, are considered to play prominent roles in uremic cardiomyopathy (12). However, previous research demonstrated that a reduction of blood pressure has little effect in preventing the development of uremic cardiac hypertrophy (13). The authors hypothesized that non-established risk factors, including uremic toxins, have been underestimated and are important in the progression of cardiovascular disease in CKD. IS is a typical protein-bound uremic toxin that cannot be removed by current hemodialysis techniques, and has been demonstrated to have a critical effect on the prognosis of cardiovascular disease induced by CKD, both in pre-clinical (5,14–16) and clinical (4,17–19) research. The conventional mechanism of pathological cardiac hypertrophy involves β-adrenergic receptor-, α-adrenergic receptor-, and Ca2+/calmodulin-related pathways, while the key mechanism of IS-induced cardiac hypertrophy is the direct induction of oxidative stress (5). It is important to further investigate the mechanism of IS-induced cardiomyocyte injury, and to explore potential therapeutic targets.

There is plenty of evidence to suggest that the key mechanism of IS cardiotoxicity is the induction of oxidative stress (5,16,20). ERS and oxidative stress are closely related in many physiological and pathological conditions (21). Protein misfolding in ERS conditions results in reactive oxygen species production, and oxidative stress disturbs the ER redox state and promotes protein misfolding (22). Therefore, the authors hypothesized that ERS may also play an important role in the harmful effects of IS. GRP78 is an ER molecular chaperone, and a specific marker of ERS (10). The present study analyzed the rate of apoptosis in H9C2 cardiomyocytes, and GRP78 protein expression, and it was demonstrated that IS dose-dependently induced ERS, and promoted the apoptosis of H9C2 cardiomyocytes. Previous studies demonstrated that, Indoxyl sulfate induces apoptosis of kidney mesangial cells (23), renal tubular cells (24,25) and osteoblast cells (26), which are in accordance with the present results. Importantly, the study showed that the ERS modulator 4-PBA attenuated the effect of IS on ERS and apoptosis induction, which indicated that the apoptosis induced by IS treatment is likely via ERS induction.

It was further demonstrated that IS increased the protein expression of GRP78, CHOP, and p-JNK, which could be suppressed by the ER inhibitor 4-PBA, and this indicating that the CHOP and JNK pathways may be associated with IS-induced ERS and apoptosis. The results identified ERS-related apoptosis as a novel mechanism in IS-induced cardiomyocyte toxicity, providing a potentially valuable therapeutic avenue for the treatment of IS-induced cardiovascular diseases.

However, various limitations of the present study should be mentioned. It is difficult to accurately recapitulate the conditions of CKD in vitro, as CKD is a long-term and complicated pathological progress, and the authors only treated cells with IS for 24 h in the present study. In addition, the concentration of IS used in the study is higher than would be expected in clinical circumstances, as a low level of IS would not cause damage in cardiomyocytes in the timeframe of the experiment. The authors intend to establish an animal model to further investigate the role of IS in uremic cardiomyopathy and its mechanism, particularly the effect on apoptosis and ERS.

In conclusion, the results suggested that IS, a protein-bound uremic toxin, induces ERS-related apoptosis in H9C2 cardiomyocytes via the CHOP and JNK pathways, and the effects were attenuated by the ERS modulator 4-PBA. The findings will aid the further understanding of the mechanisms of IS cardiotoxicity. As it is difficult to remove IS with current dialysis techniques, further findings regarding the mechanism may contribute to the development of a novel therapeutic strategy, particularly focused on ERS and apoptosis reduction.

Acknowledgements

Not applicable.

Funding

The present study was supported by the Science and Technology Commission of Shanghai Municipal (grant no. 14DZ2260200, the project of Shanghai Key Laboratory of Kidney and Blood Purification); Shanghai Committee of Science and Technology, China (grant no. 15DZ0503402); and the Shanghai Municipal Commission of Health and Family Planning (grant no. 2014 ZY3-CCCX-3-3043).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

XT and XSC performed the western blotting and flow cytometry experiments. PZ contributed to the cell culture. FFX and JT participated in experiment design and edited the manuscript. JZZ and XQD designed the present study.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References