Interleukin-2 is upregulated in patients with a prolapsed lumbar intervertebral disc and modulates cell proliferation, apoptosis and extracellular matrix metabolism of human nucleus pulposus cells
- Authors:
- Published online on: October 16, 2015 https://doi.org/10.3892/etm.2015.2809
- Pages: 2437-2443
Abstract
Introduction
The prolapse of a lumbar intervertebral disc is a common ailment that places pressure on the surrounding nerves and causes pain in the waist and leg. Intervertebral disc degeneration (IDD) has been demonstrated to be the main cause of lumbar intervertebral disc prolapse. Approximately 20% of teenage indiciduals have discs with mild signs of degeneration, while ~10% of 50-year-old individuals and ~60% of 70-year-old individuals posses discs that exhibit severe degeneration (1). However, the pathogenesis of IDD is associated with various cellular and biochemical alterations (2). IDD is associated with numerous risk factors, including lifestyle, co-morbidities, genetic predisposition and age (3).
Previous studies have detected high expression levels of cytokines in degenerated intervertebral disc tissues, including interleukin (IL)-1, interferon (IFN)-γ and tumor necrosis factor (TNF)-α, and these cytokines are associated with the pathogenesis of IDD (4–6).
IL-2, which is a pleiotropic cytokine primarily produced by T lymphocytes, has been implicated in the development and control of inflammatory disease (7,8). A previous study demonstrated that IL-2 mRNA expression was downregulated in the epidural compartment following intervertebral disc extrusion (9), and IL-2 expression levels in the disc samples of patients with lumbar degenerative disc disease were significantly increased, as compared with the controls (10). These findings suggested that IL-2 may be associated with intervertebral disc disease; however, the role of IL-2 in the cellular functions of intervertebral disc tissues remains unclear.
In the present study, the expression levels of IL-2 in the nucleus pulposus (NP) tissues, the avascular and aneural tissues in the center of the intervertebral disc, of patients with prolapsed lumbar intervertebral discs were investigated, and in vitro experiments were performed in order to investigate the role of IL-2 in the proliferation of human NP cells (HNPCs), apoptosis and extracellular matrix (ECM) metabolism. In addition, alterations in p38 mitogen-activated protein kinase (MAPK) signaling were examined in the HNPCs, a potential target for treating IDD, following IL-2 treatment.
Materials and methods
Clinical samples
The present study was approved by the Ethics Committee of The First Affiliated Hospital of Soochow University (Suzhou, China). Informed consent was obtained from all patients prior to enrollment onto the present study. Human NP tissues were obtained from 30 patients undergoing surgery for prolapsed lumbar intervertebral discs, whereas control NP tissues were obtained from 10 patients undergoing surgery for spinal trauma. The 30 patients diagnosed with prolapsed lumbar intervertebral discs included 15 males and 15 females, and the mean age was 51 years. The 10 patients with spinal trauma included 4 males and 6 females, with a mean age of 49 years.
Cell culture and treatment
HNPCs were purchased from ScienCell Research Laboratories (Carlsbad, CA, USA) and cultured in NP Cell Medium (ScienCell Research Laboratories) in an atmosphere containing 5% CO2 and 95% air. The NP Cell culture medium was changed every three days. IL-2 (Sigma-Aldrich, St. Louis, MO, USA) was dissolved in sterile distilled water, and the HNPCs were treated with 1, 5, 10 or 20 ng/ml IL-2.
Enzyme-linked immunosorbent assay (ELISA)
IL-2 expression levels in the NP tissues were determined using an IL-2 ELISA kit (R&D Systems, Inc., Minneapolis, MN, USA), according to the manufacturer's protocol. Briefly, the NP tissues were homogenized using a Dounce tissue grinder (Sigma-Aldrich) and centrifuged at 1,000 × g for 10 min at 4°C, and 100 µl of either standard, control (phosphate-buffered saline; PBS) or sample was subsequently pipetted into each well, and incubated with 100 µl assay diluent for 2 h at room temperature. Following washing, 200 µl conjugate was added and incubated for 2 h at room temperature prior to the addition of 200 µl substrate solution to develop the color. Reactions were terminated by adding 50 µl Stop solution and the absorbance was measured at 450 nm using a Multiskan Spectrum spectrophotometer (Thermo Fisher Scientific, Inc., Waltham, MA, USA).
Cell viability 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay
Cell viability was measured using an MTT assay. The cells were seeded into 96-well plates and incubated with 1, 5, 10 or 20 ng/ml IL-2 for 12, 24, 48 and 72 h, respectively. Following this, 0.5 mg/ml MTT solution (Sigma-Aldrich, St. Louis, MO, USA) was added to each well, and the plates were incubated for 4 h at 37°C. Subsequently, the medium was removed and 200 µl dimethyl sulfoxide (Invitrogen; Thermo Fisher Scientific Inc., Waltham, MA, USA) was subsequently added into each well. The absorbance was measured at 570 nm using a Multiskan Spectrum spectrophotometer (Thermo Fisher Scientific, Inc.).
Analysis of caspase-3 and caspase-8 activities
Caspase-3 and caspase-8 activities in HNPCs were measured using a Caspase Activity kit (Beyotime Institute of Biotechnology, Shanghai, China), according to the manufacturer's protocol. Briefly, the cells were washed and lysed prior to incubation of the supernatant with acetyl-Asp-Glu-Val-Asp p-nitroanilide and N-Acetyl-Ile-Glu-Thr-Asp-p-nitroanilide, respectively. The release of p-nitroaniline was determined by measuring the absorbance at 405 nm using a SpectraMax 190 microplate reading (Molecular Devices, LLC, Sunnyvale, CA, USA). The caspase activities were expressed as a percentage, relative to the control.
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
Tissues were homogenized using the Dounce tissue grinder. Total RNA was harvested from the NP tissues or the HNPCs using TRIzol® reagent (Invitrogen; Thermo Fisher Scientific Inc.), and subsequently reverse transcribed into cDNA using a First Strand cDNA Synthesis kit (Fermentas; Thermo Fisher Scientific Inc.), according to the manufacturer's instructions. The primers for RT-qPCR are outlined in Table I. PCR amplification was performed with 2 ng cDNA using a 7300 Sequence Detection system (Applied Biosystems; Thermo Fisher Scientific, Inc.) with a SYBR® Green PCR kit (Applied Biosystems; Thermo Fisher Scientific, Inc.). The cycling conditions were as follows: 5 min at 95°C, followed by 42 cycles of 5 min at 95°C, 15 sec at 58°C and 10 sec at 72°C, finally 10 min at 95°C. Relative mRNA expression levels were calculated using the 2−ΔΔCq method (11). Data are presented as fold changes, normalized to the control.
Western blot analysis
Proteins were isolated using a Total Protein Extraction kit (Nanjing KeyGEN Biotech Inc., Nanjing, China). Protein concentrations were determined using a BCA Protein Assay Kit (C503021; Sangon Biotech Co., Ltd., Shanghai, China). Total proteins (25 µg) were separated by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred via electroblotting onto polyvinylidene difluoride membranes (EMD Millipore, Billerica, MA, USA). The membranes were blocked with 5% bovine serum albumin at 4°C overnight and subsequently incubated at 37°C for 1 h with the following primary antibodies: Mouse monoclonal antibodies to p38 MAPK (#9217; 1:400), phosphorylated-p38 MAPK (#9216; 1:200) and Fas cell surface death receptor (Fas; #8023; 1:500; Cell Signaling Technology, Inc., Beverly, MA, USA); rabbit polyclonal antibody to matrix metalloproteinase (MMP)-13 (ab39012; 1:400); mouse monoclonal antibodies to collagen I (ab90395; 1:500), collagen II (ab185430; 1:500) and MMP-3 (ab17790; 1:400) Abcam, Cambridge, UK); rabbit polyclonal antibodies to a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)-4 (sc-25582; 1:800) and ADAMTS-5 (sc-83186; 1:400); and mouse monoclonal antibodies to aggrecan and glyceraldehyde 3-phosphate dehydrogenase (GAPDH; sc-365062; 1:1,000; Santa Cruz Biotechnology, Inc., Dallas, TX, USA). GAPDH was used as a housekeeping gene. Following this, the membranes were washed with PBS and incubated with a horseradish peroxidase-labeled goat anti-rabbit IgG/HRP (sc-2004; 1:5,000) and goat anti-mouse IgG/HRP (sc-2031; 1:5,000; Santa Cruz Biotechnology, Inc.) secondary antibody at 37°C for 1 h. Immunolabeling was detected using an enhanced chemiluminescence reagent and a Western Blotting kit (Pierce Biotechnology, Inc., Rockford, IL, USA). The blots were analyzed using Image-Pro Plus software (Media Cybernetics, Inc., Rockville, MD, USA)
Statistical analysis
Data were analyzed using SPSS 19.0 statistical software (IBM SPSS, Armonk, NY, USA) and presented as the mean ± standard deviation. Statistical differences between the two groups were analyzed using a Student's t-test. P<0.05 was considered to indicate a statistically significant difference.
Results
IL-2 expression levels are increased in patients with a prolapsed lumbar intervertebral disc
In order to determine the expression levels of IL-2 in the NP tissues, NP tissues were collected from the patients and controls as outlined, prior to RT-qPCR and ELISA analyses. IL-2 mRNA expression levels were significantly increased in the NP tissues of patients with a prolapsed lumbar intervertebral disc, as compared with the controls (P<0.01; Fig. 1). Furthermore, IL-2 protein expression levels were significantly increased in the NP tissues of patients with a prolapsed lumbar intervertebral disc (P<0.05; Fig. 2).
IL-2 inhibits the proliferation of HNPCs in a dose-dependent manner
To investigate the effects of IL-2 on the proliferation of HNPCs, the cells were treated with various concentration of IL-2 (1, 5, 10 and 20 ng/ml), and an MTT assay was performed. As demonstrated in Fig. 3, IL-2 inhibited the proliferation of the HNPCs in a dose-dependent manner. No significant effects on the viability of the HNPCs were observed at the lowest IL-2 concentration (1 ng/ml); however, 5, 10 and 20 ng/ml IL-2 significantly decreased the viability of the HNPCs.
IL-2 significantly increases the expression levels of apoptosis-related proteins in HNPCs
To investigate the effects of IL-2 on the apoptosis of HNPCs, the cells were treated with 20 ng/ml IL-2 for 24 h. Fas protein expression levels were analyzed by western blot analysis, and the activities of caspase-3 and −8 were analyzed in the HNPCs, using commercial kits. As demonstrated in Fig. 4, IL-2 significantly increased (P<0.05) the protein expression levels of Fas in the HNPCs; and the activities of caspase-3 and −8 were also increased in the HPNCs following treatment with IL-2 (Fig. 5A and B)
IL-2 affects ECM metabolism in HNPCs
HNPCs were treated with 20 ng/ml IL-2 for 24 h, and the mRNA expression levels of: Aggrecan; type I and type II collagen; ADAMTS-4 and −5; and MMP-3 and −13 were analyzed using RT-qPCR. As outlined in Fig. 6A, the mRNA expression levels of aggrecan were reduced by 58% following treatment with IL-2 in the HNPCs. Furthermore, following IL-2 administration, a 1.33-fold increase in the mRNA expression levels of type I collagen was detected; however, type II collagen mRNA expression levels were significantly decreased (P<0.05). Furthermore, IL-2 treatment significantly increased (P<0.05) the mRNA expression levels of ADAMTS-4 and −5, and MMP-3 and −13 (Fig. 6B).
The protein expression levels of: Aggrecan; type I and type II collagen; ADAMTS-4 and −5; and MMP-3 and −13 were examined by western blot analysis. Similar to the mRNA expression level results, IL-2 significantly increased (P<0.05) the protein expression levels of type I collagen, ADAMTS-4 and −5, MMP-3 and −13, whereas the protein expression levels of aggrecan and type II collagen were decreased (Fig. 7 and 8).
IL-2 induces the phosphorylation of p38 in HNPCs
The expression levels of p38 and its phosphorylated form were examined in the HNPCs following treatment with IL-2. As outlined in Fig. 9, the protein expression levels of p38 were not altered in response to IL-2 treatment; however, IL-2 successfully induced the phosphorylation of p38 in the HNPCs. The expression of phosphorylated-p38 protein was significantly upregulated in IL-2-treated HNPCs, as compared with the untreated control cells (P<0.05).
Discussion
The intervertebral disc contains a central NP encapsulated by endplates and the annulus fibrosus (12). The NP is an avascular and aneural tissue capable of resisting compressive loads, which acts as a pump in order to regulate the flow of liquids and gases in the disc. Therefore, the NP has a significant influence on the overall function and homeostasis of the intervertebral disc (13). In the present study, human NP tissues from patients presenting with a prolapsed lumbar intervertebral disc were harvested and the mRNA and protein expression levels of IL-2 were analyzed. The results demonstrated that IL-2 was highly upregulated in the NP tissues of patients with a prolapsed lumbar intervertebral disc, as compared with the control patients. These results suggested that IL-2 may have a pathogenic role in the prolapse of lumbar intervertebral discs.
Previous studies have demonstrated that the expression levels of cytokines, including IL-1, IL-17 and TNF-α, are elevated in pathological disc tissue, and they increase in line with the grade of degeneration (6,14). These cytokines interact with a large genetic program that is instrumental in maintaining the appropriate homeostasis of cells within the intervertebral disc. A previous in vivo study demonstrated that IL-2 is upregulated in patients with a prolapsed lumbar intervertebral disc (4); however, the mechanisms underlying the association between IL-2 and IDD have yet to be elucidated. In the present study, in order to further understand the role of IL-2 in the pathophysiological mechanisms associated with disc degeneration, in vitro experiments were performed to determine the effects of IL-2 on apoptosis, ECM metabolism and the proliferation of HNPCs.
In the present study, the HNPCs were cultured and treated with various concentrations of IL-2. An MTT assay demonstrated that IL-2 inhibits the proliferation of HNPCs in a dose-dependent manner, and 20 ng/ml IL-2 was determined to be the optimal concentration for the inhibition of HNPCs. Furthermore, 20 ng/ml IL-2 was applied to investigate the effect of IL-2 on the apoptosis and ECM metabolism of HNPCs.
The NP of the intervertebral disc contains a proteoglycan-rich ECM, which normally functions to retain water (15,16); however, degenerated intervertebral discs lose their normal architecture, leading to alterations in cell shape and biochemical characteristics. The role of apoptosis and apoptosis-related genes in the development of degenerative diseases has garnered much attention in recent years. The excessive apoptosis of NP cells, which are capable of producing ECM components, is one of the most discernable cellular and biochemical changes credited to degeneration (17–22). A previous study demonstrated that NP cells predominantly undergo apoptosis via the death receptor pathway, which contributes to degeneration of the intervertebral disc (23). The death receptor pathway is initiated by the binding of cell surface receptors, such as Fas, which activates initiator caspases, primarily caspase-8, which in turn activate effector caspases, predominantly caspase-3 (24). In the present study, IL-2 induced the expression of Fas protein and increased the activities of caspase-3 and −8 in the HNPCs, thus suggesting that the death receptor pathway may be activated by IL-2 in HNPCs in order to promote cell apoptosis.
NP cells secrete a complex ECM comprised mainly of type II collagen and proteoglycans (25). Disc degeneration results from an imbalance between the degradation and synthesis of ECM components. Alterations in collagen type, and a decrease in proteoglycan content may cause dehydration and desiccation within the NP, and the intervertebral disc may become a more fibrotic and less cartilaginous structure (26–29) as a result. Aggrecan is a large proteoglycan that forms aggregates, the loss of which is considered to be an early biochemical abnormality of IDD (30). Previous studies have demonstrated that destructive enzymes, such as MMPs or ADAMTS, are upregulated in NP cells, leading to the downregulation of aggrecan and collagen type II (31–35). In order to elucidate the effects of IL-2 on ECM metabolism in the HNPCs, the expression levels of degrading enzymes that have been demonstrated to hydrolyze aggrecan and collagen were measured. RT-qPCR and western blot analysis demonstrated that the expression levels of ADAMTS-4 and −5, and MMP-3 and −13 were significantly increased following treatment with IL-2. In addition, aggrecan expression levels were significantly decreased, and collagen was altered from type II to I. These findings suggested that IL-2 may promote ECM degradation in HNPCs.
Studer et al (36) demonstrated that the p38 MAPK signaling pathway is a potential target for the treatment of IDD. NP cells respond to inflammatory cytokines via p38 MAPK; therefore, inhibition of p38 MAPK signaling may decrease the factors that negatively affect the metabolic balance and viability of NP cells. In the present study, phosphorylated-p38 was significantly upregulated following IL-2 treatment, suggesting that IL-2 may activate p38 MAPK signaling in HNPCs.
In conclusion, the expression of IL-2 was significantly upregulated in the NP tissues of patients with a prolapsed lumbar intervertebral disc. In addition, the present study demonstrated that IL-2 inhibits cell proliferation, induces cell apoptosis and ECM degradation, and activates p38 MAPK signaling in HNPCs. These findings provide a novel insight into the molecular pathogenesis of IDD.
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