Alterations of metabolic activity in human osteoarthritic osteoblasts by lipid peroxidation end product 4-hydroxynonenal
© Shi et al.; licensee BioMed Central Ltd. 2006
Received: 26 April 2006
Accepted: 16 October 2006
Published: 16 October 2006
4-Hydroxynonenal (HNE), a lipid peroxidation end product, is produced abundantly in osteoarthritic (OA) articular tissues, but its role in bone metabolism is ill-defined. In this study, we tested the hypothesis that alterations in OA osteoblast metabolism are attributed, in part, to increased levels of HNE. Our data showed that HNE/protein adduct levels were higher in OA osteoblasts compared to normal and when OA osteoblasts were treated with H2O2. Investigating osteoblast markers, we found that HNE increased osteocalcin and type I collagen synthesis but inhibited alkaline phosphatase activity. We next examined the effects of HNE on the signaling pathways controlling cyclooxygenase-2 (COX-2) and interleukin-6 (IL-6) expression in view of their putative role in OA pathophysiology. HNE dose-dependently decreased basal and tumour necrosis factor-α (TNF-α)-induced IL-6 expression while inducing COX-2 expression and prostaglandin E2 (PGE2) release. In a similar pattern, HNE induces changes in osteoblast markers as well as PGE2 and IL-6 release in normal osteoblasts. Upon examination of signaling pathways involved in PGE2 and IL-6 production, we found that HNE-induced PGE2 release was abrogated by SB202190, a p38 mitogen-activated protein kinase (MAPK) inhibitor. Overexpression of p38 MAPK enhanced HNE-induced PGE2 release. In this connection, HNE markedly increased the phosphorylation of p38 MAPK, JNK2, and transcription factors (CREB-1, ATF-2) with a concomitant increase in the DNA-binding activity of CRE/ATF. Transfection experiments with a human COX-2 promoter construct revealed that the CRE element (-58/-53 bp) was essential for HNE-induced COX-2 promoter activity. However, HNE inhibited the phosphorylation of IκBα and subsequently the DNA-binding activity of nuclear factor-κB. Overexpression of IKKα increased TNF-α-induced IL-6 production. This induction was inhibited when TNF-α was combined with HNE. These findings suggest that HNE may exert multiple effects on human OA osteoblasts by selective activation of signal transduction pathways and alteration of osteoblastic phenotype expression and pro-inflammatory mediator production.
Lipid peroxidation (LPO) is a process initiated by lipid reaction with reactive oxygen species (ROS). ROS are generated during normal cellular metabolism or under oxidative stress stimuli (for example, cytokine and UV radiation). Polyunsaturated fatty acids of cellular membrane lipids are targets of ROS attack and undergo LPO, leading to the formation of chemically reactive lipid aldehydes capable of diffusing from their site of origin. Similar to ROS, aldehydes can cause severe damage to nucleic acids and proteins, altering their functions and leading to the loss of both structural and metabolic function of cells. Under intense oxidative stress, aldehyde levels increase and take part in numerous pathological conditions such as cancer, arthritis, arthrosclerosis, and cardiac diseases. 4-Hydroxynonenal (HNE) is the principal α, β-unsaturated aldehyde formed from LPO of both ω-3 and ω-6 polyunsaturated fatty acids. The accumulation of HNE exhibits a wide range of biological activities, including stimulation of neutrophil migration, mitochondrial enzyme inhibition, and activation of stress-signaling pathways via transcription factors and protein kinase pathways, as well as inhibition of the nuclear factor-κB (NF-κB) signaling pathway [3–6].
Osteoarthritis (OA) is a degenerative disease characterised by a progressive degradation of articular cartilage accompanied with secondary inflammation of synovial membranes. Although major progress has been made in the last few years, the aetiology, pathogenesis, and progression of this disease are not fully understood. Recent clinical and research findings suggest that oxidative stress-induced LPO products can play an important role in the pathogenesis of OA. Grigolo and colleagues  were the first to demonstrate that the formation of HNE and malondialdehyde (MDA) is enhanced in synoviocytes from patientswith OA. In a recent study, we have shown that HNE level is higher in synovial fluids of patients with OA compared with normal subjects and in human articular OA chondrocytes exposed to ROS donors. In addition, we have reported novel mechanisms linking HNE to OA cartilage degradation. These mechanisms emphasise the implication of HNE in transcriptional and post-translational modifications of type II collagen and matrix metalloproteinase-13 in human OA chondrocytes, and result in cartilage extracellular matrix (ECM) degradation. However, little is known about the role of HNE in bone.
Abnormal subchondral trabecular bone remodelling is present in patients with OA. The increased stiffness of OA bone with subchondral bone plate sclerosis results in increased trabecular thickening and decreased trabecular space volume/bone mineralisation with the bone cell defects. Type 1 collagen (Col I) and other specific osteoblast phenotypic markers, such as osteocalcin (OC) and alkaline phosphatase (ALPase), are released from osteoblasts during bone formation. It is believed that alterations in osteoblast metabolism play an important role in this disease by producing excess bone-resorbing cytokines and prostaglandins. Among the pro-inflammatory mediators, interleukin-6 (IL-6) is a multifunctional cytokine involved in osteoclast recruitment and differentiation into mature osteoclast. Prostaglandin E2 (PGE2), produced primarily by cyclooxygenase-2 (COX-2) , plays an important role in the local regulation of bone formation and bone resorption. These biologically active mediators are also considered to be biochemical markers of bone metabolism and are regulated in bone by pro-inflammatory cytokines.
The objective of this study was to investigate the role of HNE in OA osteoblast metabolism by determining its effect on the production of biological markers and pro-inflammatory mediators. Furthermore, we explored the signaling pathways involved in HNE-regulated IL-6 and PGE2 production.
Materials and methods
Normal human osteoblasts were purchased from PromoCell GmbH (Heidelberg, Germany) and were cultured according to the manufacturer's specifications. OA osteoblasts were isolated from trabecular bone specimens from patients suffering from advanced OA and undergoing primary total knee replacement. The experimental protocol was approved by the Research Ethics Board at Sacre-Cæur Hospital of Montreal. The osteoblast cell cultures were prepared as already described. Briefly, trabecular bone samples were cut into small pieces of 2 mm2 prior to their sequential digestion in the presence of 1 mg/ml collagenase type I (Sigma-Aldrich Canada Ltd., Oakville, ON, Canada) in BGJb media (Invitrogen Canada Inc., Burlington, ON, Canada) without serum at 37°C for 30, 30, and 240 minutes. After being washed with the same media, the digested bone pieces were cultured in 25 cm2 plastic cell culture flasks (Corning Incorporated, Corning, NY, USA) with BGJb media containing 20% foetal bovine serum (FBS) (Invitrogen Life Technologies). This medium was replaced every 2 days until cell outgrowths appeared around the explants. At confluence, cells were split once and plated at 50,000 cells per cm2 in culture plates (Falcon, Lincoln Park, NJ, USA) with Ham's F-12/Dulbecco's modified Eagle's medium (HAMF-12/DMEM) (Sigma-Aldrich Canada Ltd.) containing 10% FBS and 50 mg/ml ascorbic acid and grown to confluence again. Only first-passage cells were used in our experiments.
Normal and OA osteoblasts were incubated for 24 hours with or without increasing concentrations of H2O2 (1 to 100 μM). Total cellular levels of HNE/protein adducts were assessed in cellular extracts of osteoblasts using an in-house enzyme-linked immunosorbent assay (ELISA) as previously described .
Determination of OC level and ALPase activity
Osteoblasts were incubated for 24 hours in HAMF-12/DMEM containing 2% charcoal-stripped FBS, which yields maximal stimulation of ALPase activity and OC secretion. Cells were then incubated for 48 hours in the same medium in the presence of increasing concentrations of HNE (0 to 20 μM). The medium was collected at the end of the incubation and frozen at -80°C prior to assay. Cells were washed twice with phosphate-buffered saline, pH 7.4, and solubilised in ALPase buffer (100 mM glycine, 1 mM MgCl2, 1 mM ZnCl2, 1% Triton X-100; pH 10.5) for 60 minutes with agitation at 4°C. Cellular ALPase activity was determined as the release of p-nitrophenol hydrolysed from p-nitrophenyl phosphate (12.5 mM final concentration) at 37°C for 30 minutes after cell solubilisation in ALPase buffer as described above. Protein determination was performed by the bicinchoninic acid method. Nascent OC was determined by a specific enzyme immunoassay (Biomedical Technologies, Inc., Stoughton, MA, USA). The detection limit of this assay is 0.5 ng/ml, and 2% charcoal-treated FBS contains less than 0.1 ng/ml of OC.
IL-6 and PGE2assays
For the HNE dose-response curves, osteoblasts were incubated in 0.5% FBS/HAMF-12/DMEM for 48 hours with increasing concentrations of HNE (0 to 20 μM). After incubation, the culture medium was collected and the IL-6 and PGE2 levels were determined using specific commercial kits from R&D Systems, Inc. (Minneapolis, MN, USA) and Cayman Chemical Company (Ann Arbor, MI, USA), respectively, according to the manufacturers' specifications. The sensitivities of the assays were 3 and 9 pg/ml, respectively.
Protein detection by Western blotting
Osteoblasts were incubated in fresh medium containing 0.5% FBS/HAMF12/DMEM in the presence of increasing concentrations of HNE (0 to 20 μM) for 24 hours or in the presence of 20 μM of HNE for increasing periods of incubation. Twenty to 50 μg of cellular protein extract was subjected to discontinuous 4% to 12% SDS-PAGE under reducing conditions and transferred onto nitrocellulose membrane (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The membranes were immersed overnight at 4°C in a blocking solution consisting of TTBS (20 mM Tris, pH7.4, 150 mM NaCl, 0.1% Tween 20) and 5% skim milk and incubated again overnight in blocking buffer containing the polyclonal rabbit anti-COX-2 or anti-Col I (1:1,000 dilution; Oncogene Research Products, San Diego, CA, USA). The membranes were then washed three times with TTBS and incubated for 1 hour at 22°C with the second antibody (anti-rabbit immunoglobulin G-horse radish peroxidase; New England Biolabs Ltd., Mississauga, ON, Canada) and washed again. Detection was carried out using Supersignal west dura extended duration substrate (Pierce Biotechnology, Inc., Rockford, IL, USA). Membranes were prepared for autoradiography and exposed to clear-blue x-ray film (Pierce) and then subjected to a digital imaging system (Bio-Rad Laboratories, Inc.). For the total and phosphorylated level of mitogen-activated protein kinases (MAPKs) (p38, c-Jun NH2-terminal kinase [JNK] 1/2, and extracellular signal-regulated kinase [ERK] 1/2) as well as transcription factors (activating transcription factor-2 [ATF-2], CRE-binding factor-1 [CREB-1], and IκBα), we used specific PhosphoPlus kits (New England Biolabs Ltd.).
Real-time quantitative reverse transcriptase-polymerase chain reaction
Total RNA was extracted from OA osteoblasts using TRIzol® reagent (Invitrogen Life Technologies) according to the manufacturer's recommendations. The RNA was quantitated using the RiboGreen RNA quantitation kit (Molecular Probes, now part of Invitrogen, Carlsbad, CA, USA), dissolved in RNase-free H2O, and stored at -80°C until use. One microgram of total RNA was reverse-transcribed using Moloney murine leukaemia virus reverse transcriptase (Fermentas Canada Inc., Burlington, ON, Canada) as detailed in the manufacturer's guidelines. One fiftieth of the reverse transcriptase reaction was analysed by real-time quantitative polymerase chain reaction (PCR). The nucleotide sequence of primers are shown below:
ALPase : 5'-CCCAAAGGCTTCTTCTTG-3' (sense)
OC : 5'-ATGAGAGCCCTCACACTCCTC-3' (sense)
Col I α 1 : 5' CATCCTCGACGGCATCTCAGC-3' (sense)
IL-6 : 5'-TTCAAATGAGATTGTGGGAAAATTGCT-3' (sense)
COX-2 : 5'-TTCAAATGAGATTGTGGGAAAATTGCT-3' (sense)
5'-AGTTCATCTCTGCCTGAGTATCTT-3' (anti-sense), and
glyceraldehyde-3-phosphate dehydrogenase (GAPDH) :
5'-CAG AAC ATC ATC CCT GCC TCT-3' (sense)
5'-GCT TGA CAAAGT GGT CGT TGA G-3' (anti-sense).
Quantitative PCR analysis was performed in a total volume of 50 μl containing template DNA, 200 nM of sense and antisense primers, 25 μl of SYBR® Green master mix (Qiagen Inc., Mississauga, ON, Canada), and uracil-N-glycosylase (UNG) (0.5 Units; Epicentre Biotechnologies, Madison, WI, USA). After incubation at 50°C for 2 minutes (UNG reaction) and at 95°C for 10 minutes (UNG inactivation and activation of the AmpliTaq Gold enzyme), the mixtures were subjected to 40 amplification cycles (15 seconds at 95°C for denaturation and 1 minute for annealing and extension at 60°C). Incorporation of SYBR® Green dye into PCR products was monitored in real time using a GeneAmp 5700 Sequence detection system (Applied Biosystems, Foster City, CA, USA) allowing determination of the threshold cycle (CT) at which exponential amplification of PCR products begins. After PCR, dissociation curves were generated with one peak, indicating the specificity of the amplification. The CT value was obtained from each amplification curve using the software provided by the manufacturer (Applied Biosystems). Preliminary experiments showed that the amplification efficiency of COX-2, ALPase, OC, Col α1, IL-6, and GAPDH was similar.
Relative amounts of mRNA in normal and OA cartilage were determined using the standard curve method. Serial dilutions of internal standards (plasmids containing cDNA of target genes) were included in each PCR run, and standard curves for the target gene and for GAPDH were generated by linear regression using log (CT) versus log (cDNA relative dilution). The CT values were then converted to number of molecules. Relative mRNA expression in cultured chondrocytes was determined using the ΔΔCT method, as detailed in the manufacturer's guidelines (Applied Biosystems). A ΔCT value was first calculated by subtracting the CT value for the housekeeping gene GAPDH from the CT value for each sample. A ΔΔCT value was then calculated by subtracting the ΔCT value of the control (unstimulated cells) from the ΔCT value of each treatment. Fold changes compared with the control were then determined by raising 2 to the ΔΔCT power. Each PCR reaction generated only the expected specific amplicon as shown by the melting-temperature profiles of the final product and by gel electrophoresis of test PCR reactions. Each PCR was performed in triplicate on two separate occasions for each independent experiment.
Nuclear extract preparation and electrophoretic mobility shift assay
OA osteoblasts were incubated with HNE alone or in combination with 1 ng/ml tumour necrosis factor-α (TNF-α) for 1 hour. Nuclear extracts were prepared and electrophoretic mobility shift assay (EMSA) was performed as previously described. Double-stranded oligonucleotide probes for CRE (5'-AGAGATTGCCTGACGTCAGAGAGCTAG-3') and NF-κB (5'-AGTTGAGGGGACTT TCCCAGGC-3') were end-labeled with [γ-32P]-ATP using a kit (Promega Corporation, Madison, WI, USA). The binding reactions were conducted with 5 μg of nuclear extract and of 2 × 105 cpm of [γ-32P]-labeled oligonucleotide probe at 22°C for 20 minutes in a final volume of 10 μl, and complexes were resolved on non-denaturing 6% polyacrylamide gels. Then, gels were fixed, dried, and exposed to clear-blue x-ray film (Pierce).
Supershift assays were performed as described above with nuclear extracts from cells treated with HNE (20 μM) or TNF-α (1 ng/ml) for 1 hour. Two micrograms of the antibodies were added to the shift reaction mixture 20 minutes after the incubation period, followed by another incubation at 4°C overnight. The antibodies were specific for the transcription factors ATF-2, p65, and p50 (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA).
Plasmids and transient transfections
The human COX-2 promoter constructs used included a wild-type (WT) (-415)-Luciferase (Luc) COX-2 promoter plasmid, mutated ATF/CRE (-58/-53) (-415)-Luc COX-2 promoter plasmid, and mutated NF-κB (-223/-214) (-415)-Luc COX-2 promoter plasmid, as previously described . Expression vectors for WT (pCMV-Flag-p38) and dominant negative (DN) (pCMV-Flag-p38) p38 MAPK were a kind gift from Dr. R.J. Davies (University of Massachusetts). Expression vector for IKKα was generously given by Dr. M. Karin (University of California). A pCMV-β-galactosidase (pCMV-β-gal) reporter vector was purchased from Promega Corporation.
Human MG-63 osteoblast-like line cells (American Type Culture Collection, Manassas, VA, USA) (approximately 50% confluence) were transiently transfected in 12-well cluster plates using lipofectamine 2000™ reagent methods (Invitrogen Life Technologies) according to the manufacturer's protocol. Briefly, transfections were conducted for 6 hours with DNA lipofectamine complexes containing 10 μl of lipofectamine reagent, 2 μg DNA plasmid, and 0.5 μg of pCMV-β-gal (as a control of transfection efficiency). After washing, medium was replaced by a fresh medium containing 1% FBS and experiments were performed in this medium supplemented with the factors under study. For promoter study, Luciferase activity was determined in cellular extracts by a kit (Luciferase Assay System; Promega Corporation) using a microplate luminometer (Applied Biosystems) and normalised to β-gal level, which was quantified by a specific ELISA (Roche Diagnostics Canada, Laval, QC, Canada). To study the effect of p38 MAPK and IKKα overexpression on PGE2 and IL-6 production, cells were transfected with the appropriated WT p38 MAPK, DN p38 MAPK, or IKKα expression vector as described above and then culture medium was collected for PGE2 and IL-6 assay as described above.
The data are expressed as the mean ± standard error of the mean. Statistical significance was assessed by unpaired Student t test, and P < 0.05 was considered significant.
HNE production in OA osteoblasts
Changes in differentiation markers (ALPase and OC) and Col I
In contrast to the inhibition of ALPase, OC protein level was increased significantly in the presence of HNE (15%, 25%, and 20% at 5, 10, and 20 μM, respectively; p < 0.05) (Figure 2c). OC mRNA levels were also increased at different concentrations of HNE, with a maximum stimulation of 155% at 5 μM HNE (p < 0.01) (Figure 2d).
Finally, we explored the effect of HNE on Col I, which constitutes 90% of the total organic ECM in mature bone. Our data showed that HNE increased Col I protein expression by factors of 2.4, 2.1, 4.6, and 8.4 at concentrations of 1, 5, 10, and 20 μM, respectively (Figure 2e), although this inductive effect of HNE was not manifested at the mRNA level (Figure 2f).
HNE inhibits IL-6 expression
HNE induces PGE2release and COX-2 expression
To delineate the signaling pathways involved in HNE-induced COX-2 expression in pilot experiments, we used cell-permeable chemical inhibitor of p38 MAPK, SB202190. This inhibitor had no effect on the basal PGE2 release (data not shown). As shown in Figure 4d, HNE significantly induced PGE2 release by 340% in comparison with untreated cells. However, the p38 MAPK inhibitor significantly reduced HNE-stimulated PGE2 production. Identical results were obtained with COX-2 protein level (data not shown).
HNE modulates ALPase, OC, IL-6, and PGE2in normal osteoblasts
HNE activates p38 MAPK and JNK1/2, but not ERK1/2
HNE induced ATF-2/CREB activation but inhibited NF-κB
Next, we investigated the effect of HNE on p38 MAPK downstream transcription factors CREB-1 and ATF-2. Our data showed that exposure of 20 μM HNE resulted in an early phosphorylation of ATF-2 and CREB-1 after 5 minutes of incubation (Figure 6a). We also examined the effect of HNE on the total NF-κB/p65 and phosphorylated IκBα. Our data showed that HNE had no significant effect on the basal level of the phosphorylated IκBα and cytosolic and nuclear NF-κB/p65 in osteoblasts (data not shown). However, combined with TNF-α, HNE inhibited strongly NF-κB/p65 protein translocation in the nucleus in a dose-dependent manner (Figure 6b).
HNE increased DNA binding of ATF/CRE, but decreased DNA binding of NF-κB
To explore the effect of HNE on DNA-binding activity of ATF/CRE and NF-κB, OA osteoblasts were incubated for 60 minutes with 20 μM HNE or 1 ng/ml TNF-α. The latter was used as a positive control of NF-κB activation. EMSA data showed that HNE increased the DNA-binding activity of ATF/CRE to 170% compared with unstimulated cells (Figure 6c). However, TNF-α (but not HNE) induced the DNA-binding activity of NF-κB by 160% (Figure 6d). Basal and induced binding was displaced by adding 50-fold excess cold ATF/CRE and NF-κB oligonucleotide (competition).
To further identify the ATF/CRE and NF-κB protein complexes that bind on these motifs, specific anti-ATF-2, anti-p65, and anti-p55 antibodies were added to the shift reaction mixture. As illustrated in Figure 6c,d, the ATF-2 was supershifted in HNE-treated osteoblasts, and the p65 and p50 proteins were supershifted in TNF-α-treated osteoblasts.
HNE induced COX-2 promoter activity via CRE site
IL-6 and PGE2modulation by HNE is related to IKKα and p38 MAPK signaling pathways, respectively
To further confirm that p38 MAPK plays a principal role in mediating HNE-induced COX-2 in osteoblasts, we transfected expression vectors of WT p38 MAPK and DN p38 MAPK followed by HNE stimulation. Overexpression of WT p38 plasmid markedly increased PGE2 production, and HNE treatment further enhanced PGE2 release compared with control cells (Figure 8b). However, the overexpression of DN p38 MAPK abrogated this effect.
This study was aimed at clarifying the regulation of OA osteoblast activity by HNE, a very reactive aldehyde produced during ROS-induced LPO. One major finding of this study was an alteration in the production of ALPase, OC, and Col I by osteoblasts after HNE exposure. Also, HNE up to 20 μM did not alter the cell viability but at 50 μM was cytotoxic and significantly decreased the cell viability (approximately 40%) compared with untreated cells (data not shown). Based on these data, all subsequent experiments were conducted using HNE up to 20 μM. The mechanism of HNE cytotoxicity was demonstrated in various cell types and tissues and is believed to be related to the chemical modification of cellular proteins by HNE. Among a number of proteins modified by HNE, citric acid cycle enzymes and cytochrome C oxidase were detected as the major targets of HNE in cells[5, 24, 25]. On the other hand, exposure of cells to HNE resulted in rapid reduction of cellular glutathione levels, suggesting that HNE influences primarily the redox status of the cells.
Firstly, we demonstrated that HNE (at ≤10 μM) reduced ALPase activity without changing its expression. These data suggest the existence of a post-translational mechanism that decreases ALPase activity, possibly through HNE binding. This is based on previous reports showing that H2O2 and glucose mediate post-translational modification of this enzyme and, in turn, enzyme inactivation[27, 28]. Because bone ALPase is a transmembrane protein, and the membrane is a source of HNE production by LPO process, we suggest that ALPase would be more susceptible to attack by this aldehyde. With the ultimate goal of determining whether ALPase was a target for HNE, we have incubated bovine recombinant ALPase with increasing concentrations of HNE. Our preliminary data showed that this aldehyde inhibits enzyme activity in a dose-dependent manner (study in progress). Given that ALPase is one of the markers of osteoblast phenotypic differentiation and plays an important role in bone formation, the observed decrease in its activity in response to HNE exposure supports the hypothesis that this molecule prevents osteoblast differentiation/mineralisation. Our data are in agreement with those of Parhami and colleagues  and Mody and colleagues , showing that lipid oxidation products inhibit osteoblastic differentiation of marrow stromal cells as demonstrated by inhibition of ALPase activity. ALPase participates in the differentiation of osteoblasts and provides phosphate for hydroxyapatite mineral formation. Its inhibition by HNE could therefore lead to impaired bone mineralisation.
Secondly, in contrast to ALPase, OC expression at protein and mRNA levels was significantly increased after treatment with HNE (1 to 20 μM). OC is synthesised predominately by osteoblasts and represents the most osteoblast-specific gene. Glowacki and colleagues  supported the hypothesis that OC may function as a matrix signal in the recruitment and differentiation of bone-resorbing cells. Because OC is limited to the osteoblast, analysis of its expression in vitro provides important information about terminal osteoblast differentiation . Increased bone formation is observed in OC knockout mice. These findings underline the importance of OC in bone turnover, suggesting that OC retards bone formation/mineralisation. Therefore, the increased OC levels in HNE-treated osteoblasts indicate that HNE plays an important role in regulation of osteoblastic bone formation functions.
Thirdly, we demonstrated that HNE induces Col I α1 expression in human osteoblasts at the protein, but not at the mRNA, level. This may indicate that HNE upregulates Col I synthesis at the post-transcriptional step, but we cannot explain this finding at this time. Further investigations will be performed to explain why HNE does not affect the mRNA level of Col I by determining RNA-binding proteins. Among them, alphaCP protein was identified as having a critical role in mRNA stabilisation of Col I. The induction of Col I synthesis by HNE in osteoblasts suggests that this aldehyde contributes to the elevation of collagen deposition in OA bone and supports other reports. Parola and colleagues  were the first to demonstrate that HNE upregulates Col I in human hepatic fat-storing cells. In another study, Garcia-Ruiz and colleagues  demonstrated that MDA upregulates Col I through activation of Sp1 transcription factor. It has been reported that HNE acted as a potent pro-fibrogenic stimuli in the expression of genes involved in ECM deposition in hepatic fat-storing cells . Nevertheless, our findings that HNE potentially acts as a pro-fibrogenic stimulus to induce Col I production in osteoblasts suggest a possible link between oxidant stress and OA trabecular subchondral bone fibrosis.
In our study, we considered it essential to address several potential factors, such as IL-6 and PGE2, that play a critical role in bone resorption. Our previous study reported that OA subchondral and trabecular osteoblasts produce more IL-6 and PGE2 levels than normal cells. We demonstrate here that HNE inhibits basal and TNF-α-induced IL-6 expression at both protein and mRNA levels in osteoblasts via the NF-κB signaling pathway. We have detected significant changes in total IκBα and a slight decrease of phosphorylated IκBα. Moreover, no translocation of NF-κB/p65 from cytosol to the nucleus was observed in HNE-treated osteoblasts. This observation was confirmed by NF-κB-binding activity and IKKα overexpression. We demonstrated that HNE inhibits TNF-α-induced NF-κB binding. Interestingly, HNE completely blocked the IKKα-enhanced TNF-α-induced IL-6 production. These data are consistent with other studies suggesting that HNE exerts its inhibitory action at the IKKα level or upstream, thereby affecting subsequent IκBα phosphorylation/proteolysis. The inhibition of NF-κB system by HNE and prevention of degradation of IκBα are associated with certain alterations of expression of the NF-κB target gene product, such as inducible nitric oxide synthase  and IL-6. As indicated, the regulation of IL-6 expression is governed predominantly by the ubiquitously expressed transcription factor NF-κB, which is required for the inducible expression of genes associated with inflammatory responses. The report of Dendorfer and colleagues  indicated that mutations in the NF-κB site of IL-6 promoter completely abolished lipopolysaccharide-induced promoter activity in murine monocyte-macrophage cell line PU5-1.8. Altogether, our findings combined with the existing literature indicate that HNE inhibits IL-6 expression at the transcriptional level via NF-κB signaling pathways.
COX-2 and PGE2 levels were markedly increased in osteoblasts treated with HNE. We demonstrated that the p38 MAPK pathway played a key role in the mechanism of HNE-induced PGE2 expression. We observed that HNE stimuli elicited a rapid and significant phosphorylation of p38 MAPK in osteoblasts. Next, we tested the effect of a p38 MAPK-specific inhibitor, SB202190, on PGE2 release. Our data showed that SB202190 blocked completely the HNE-induced PGE2 production. Furthermore, the overexpression of WT p38 MAPK enhanced PGE2 expression, and conversely DN p38 MAPK decreased HNE-induced PGE2 levels. Kumagai and colleagues have proposed for the first time the implication of p38 MAPK in HNE-induced COX-2 in epithelial cells. The authors have demonstrated that HNE enhances COX-2 expression by the stabilisation of COX-2 mRNA via the p38 MAPK pathway. In COX-2 promoter, numerous cis-elements are identified to exert transcriptional control of COX-2[22, 44]. Among these elements, ATF/CRE was shown to act as the most critical of these regulatory elements for COX-2 transcription. Mutation in the ATF/CRE sequence attenuates HNE-stimulated COX-2 promoter activity. Mutating the more proximal NF-κB in the human COX-2 promoter construct was without effect in the basal and HNE-stimulated luciferase activity, suggesting that the NF-κB site in the promoter region of COX-2 gene is not involved in the HNE-induced COX-2 expression. In many cell types, the ATF/CRE site is activated by homodimers and heterodimers of c-Jun, c-Fos, and ATF/CRE family members subsequent to serum, 12-O-tetradecanoylphorbol-13-acetate, or growth factor stimulation. HNE was shown to induce ATF-2 and CREB-1 phosphorylation and DNA-binding activity of the ATF/CRE site. Under different cytokines and growth factors, NF-κB and ERK1/2 are known regulators of COX-2 expression[45, 46]. However, neither IκBα degradation nor translocalisation of NF-κB from cytoplasm to the nucleus was observed by western blotting analysis and ERK1/2 kinase was not phosphorylated by HNE treatment. This observation indicates that NF-κB and ERK1/2 are not involved in the HNE-induced COX-2 expression.
In this study, we identified for the first time a novel mechanism linking oxidative stress to nuclear signaling in OA osteoblasts through the action of HNE, an LPO end product. Our data suggest that HNE may contribute in OA development via its ability to alter cellular phenotype and metabolic activity of osteoblasts. In the light of the previous data on increased HNE levels in OA articular tissues, particular interest should be addressed to the pathophysiological role of this aldehyde in OA.
= alkaline phosphatase
= activating transcription factor-2
- Col I:
= type I collagen
= CRE-binding factor-1
= threshold cycle
= dominant negative
= extracellular matrix
= enzyme-linked immunosorbent assay
= extracellular signal-regulated kinase
= foetal bovine serum
= glyceraldehyde-3-phosphate dehydrogenase
= IkappaB kinase alpha
= c-Jun NH2-terminal kinase
= mitogen-activated protein kinase
= nuclear factor-κB
= lipid peroxidation
= polymerase chain reaction
= prostaglandin E2
= reactive oxygen species
= tumour necrosis factor-α
- TTBS = 20 mM Tris:
pH7.4, 150 mM NaCl, 0.1% Tween 20
We would like to thank Drs. M. Karin and R.J. Davis for their respective generous gifts of the IKKα/β and p38 MAPK expression plasmids. This study was supported by Fonds de la recherche en santé du Québec (FRSQ) (grant no. 5330). MB is a research scholar at the FRSQ.
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