Apoptosis is not the major death mechanism induced by celecoxib on rheumatoid arthritis synovial fibroblasts
© Audo et al.; licensee BioMed Central Ltd. 2007
Received: 11 May 2007
Accepted: 12 December 2007
Published: 12 December 2007
Synovial hyperplasia in rheumatoid arthritis (RA) has been associated with apoptosis deficiency of RA fibroblast-like synoviocytes (FLSs). Celecoxib is a non-steroidal anti-inflammatory drug that has been demonstrated to induce apoptosis in some cellular systems. We have therefore examined the dose- and time-dependent effects of celecoxib on RA FLS viability. Treatment of RA FLSs with celecoxib for 24 hours reduced their viability in a dose-dependent manner. Analysis of celecoxib-treated RA FLSs for their content of apoptotic and necrotic cells by Annexin V staining and TO-PRO-3 uptake displayed only few apoptotic cells. Caspase 3, a key mediator of apoptosis, was not activated in celecoxib-treated RA FLSs, and the presence of specific caspase 3 or pan-caspase inhibitors did not affect celecoxib-induced cell death. Moreover, we could not detect other signs of apoptosis, such as cleavage of poly(ADP-ribose) polymerase, caspase 8 or 9, or DNA fragmentation. We therefore conclude that apoptosis is not the major death pathway in celecoxib-treated RA FLSs.
Cyclooxygenases (COXs) are key enzymes in the conversion of arachidonic acid to prostanoids, which mediate mitogenesis, apoptosis, angiogenesis, blood flow, secondary injury (lipid peroxidation and oxidative stress), and inflammation . The COX-1 isoform is constitutively expressed under physiological conditions, whereas expression of the COX-2 isoform is inducible under pathophysiological, mainly inflammatory, conditions . Consequently, the current pharmacological strategy is to selectively inhibit COX-2 and thereby avoid unfavorable effects of combined COX-1 and COX-2 blocking [1, 2].
Rheumatoid arthritis (RA) is an autoimmune disease characterized by chronic inflammation of joints, leading to a progressive and irreversible joint destruction [3, 4]. The aggressive front of synovial tissue, called pannus, invades and destroys the local articular structure [3, 4]. The pannus is characterized by a synovial hyperplasia that is mainly composed of fibroblast-like synoviocytes (FLSs) combined with a massive infiltration of lymphocytes and macrophages [3, 4]. Increased proliferation and insufficient apoptosis might contribute to the expansion of RA FLSs, and several reports suggest inducing apoptosis of RA FLSs as a therapeutic approach [3, 4].
Celecoxib (4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl] benzenesulfonamide) is an anti-inflammatory drug that specifically inhibits the COX-2. Celecoxib has been described as a pro-apoptotic factor in several human carcinoma cells [5–7]. In addition, it has been reported that high doses of celecoxib have a pro-apoptotic effect on RA FLSs . Here, we report that the cell death induced by high doses of celecoxib on RA FLSs is rapid without displaying characteristics of apoptosis.
Materials and methods
Celecoxib and valdecoxib were generously provided by Pfizer Inc (New York, NY, USA) and dissolved in dimethyl sulfoxide (DMSO) at 100 mM. Indomethacin (Sigma-Aldrich, St Quentin Fallavier, France) was dissolved in ethanol at a final concentration of 100 mM. Pan-caspase inhibitor (z-VAD-fmk [benzyloxycarbonyl-Val-Ala-Asp (OMe) fluoromethylketone]), caspase 3 inhibitor (z-DEVD-fmk [benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-FMK inhibitor]), and the caspase control inhibitor z-FA-fmk (benzyloxycarbonyl-phenyl-alanyl-fluoromethylketone) specific for cathepsins B and L (R&D Systems, Lille, France) were dissolved at 20 mM in DMSO. Annexin V was purchased from Roche Diagnostic (Meylan, France) and TO-PRO-3 from Invitrogen Corporation (Cergy Pontoise, France). Anti-caspase antibodies were obtained from Cell Signaling Technology (St Quentin Yveline, France), poly(ADP-ribose) polymerase (PARP) antibody from BD Pharmingen (BD Biosciences, Le-Pont-de-Claix, France), and peroxidase-conjugated secondary antibodies were purchased from Sigma-Aldrich.
Preparation of fibroblast-like synoviocytes of patients with rheumatoid arthritis
Fibroblasts were isolated from synovium obtained from patients who met the American College of Rheumatology criteria for RA (revised 1987) and who had undergone surgery for synovectomy or total joint replacement surgery . Fresh synovial tissues were minced and digested in a solution of dispase (Gibco, now part of Invitrogen Corporation) and collagenase (Sigma-Aldrich) and DNase (Calbiochem, now part of EMD Biosciences, Inc., San Diego, CA, USA). Synovial fibroblasts were cultured in RPMI 1640 supplemented with 10% fetal calf serum (FCS). Cells were used at passages 4 to 10, when they constitute a homogeneous population of fibroblasts, free of detectable T cells or macrophages. Upon reaching confluence, the cells were passaged by brief trypsinization. For experimentation, the content of FCS in the media was progressively decreased from 10% to 1% with final starvation for 12 hours in RPMI 1640 media containing 1% FCS, as described previously .
Analysis of cell viability and apoptosis
Cell viability was measured by taking metabolic activity as a readout using the Celltiter 96 AQueous cell proliferation (MTS) assay (Promega Corporation, Charbonnières, France) after 24 hours of cell culturing according to the manufacturer's instructions. Apoptotic RA FLSs were identified by resuspending 1 × 105 cells in 100 μL of Annexin V Binding buffer containing 5 μL of Annexin V-fluorescein isothiocyanate (10 μg/mL; R&D Systems) for 15 minutes at room temperature. Upon addition of TO-PRO-3 (1:2,000), cells were analyzed by flow cytometry (FACSCalibur; BD Biosciences) .
Cell proliferation assay
Proliferation was evaluated measuring DNA synthesis by incorporation of tritiated [3H]thymidine. FLSs were seeded in 96-well flat-bottom culture plates at a density of 1 × 104 cells per well. Cells were cultured in RPMI 1640 with decreasing concentrations of FCS (10% and 5%) and then synchronized for 24 hours with RPMI 1640 and 1% FCS. FLSs were stimulated for 72 hours. Every condition was tested in quadruplicate. [3H]thymidine (1 μCi/well) was added 24 hours before the end of the assay. FLSs were lysed using a round of freeze-thaw cycle and then transferred onto a membrane filter using Harvester 96 (Tomtec, Hamdem, CT, USA). [3H]thymidine incorporated into DNA was quantified using a scintillation counter 1450 MicroBeta Trilux (Wallac, now part of PerkinElmer Life and Analytical Sciences, Inc., Waltham, MA, USA').
Western blotting analysis
Synovial cells were seeded in six-well plates at 2 × 105 cells per well or in 6-cm dishes at 4 × 105 cells. After serum starvation, RA FLSs were treated as indicated. Both detached and adherents cells were collected, washed twice with cold phosphate-buffered saline (PBS), and treated with lysis buffer as described previously . Total cell extracts were resolved by SDS-PAGE and proceeded for immunoblot analysis as described previously . Primary antibodies were diluted according to the manufacturer's instructions (1:1,000 dilutions for anti-caspase and anti-PARP antibodies and 1:5,000 dilution for anti-β-actin antibody), and nitrocellulose membranes were incubated overnight at 4°C with the primary antibodies (or for 1 hour at room temperature for β-actin). Equal loading was confirmed by β-actin expression.
Ac-DEVD-AMC (caspase 3/7 fluorogenic substrate) protease assay
Synovial fibroblasts were seeded in six-well plates at 2 × 105 cells per well. After serum starvation, RA FLSs were treated with either celcoxib or tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), and caspase 3 activation was measured using the Ac-DEVD-AMC protease assay according to the manufacturer's instructions (BD Biosciences).
FLSs were seeded in 96-well flat-bottom culture plates at 1 × 104 cells per well, cultured with decreasing concentrations of FCS (10%, 5%, and 1%) as described above, and incubated for 12 hours with either celecoxib or TRAIL. Cells were collected, washed with PBS, and processed for quantification of DNA fragments using an enzyme-linked immunosorbent assay according to the manufacturer's instructions (Cell Death Detection ELISAPLUS; Roche Diagnostic).
Celecoxib decreases cell activity and proliferation of rheumatoid arthritis fibroblast-like synoviocytes
The decreased viability of celecoxib-treated RA FLSs was mirrored by their decreased proliferation capacity as measured by thymidine incorporation. Celecoxib inhibited RA FLS proliferation in a dose-dependent manner at all of the concentrations tested (20, 40, 50, and 60 μM), and only marginal thymidine incorporation was detectable in the presence of 60 μM celecoxib (Figure 1b).
Celecoxib-treated rheumatoid arthritis fibroblast-like synoviocytes bypass the state of early apoptosis
No caspase activity is detectable in celecoxib-treated rheumatoid arthritis fibroblast-like synoviocytes
One mechanism that is consistently implicated in apoptosis is the activation of a cascade of cytosolic proteases called caspases. Caspases are synthesized as inactive proenzymes that are processed by proteolytic cleavage to form an active enzyme. A member of this family, caspase 3 (CPP32, apopain, and YAMA), plays a central role in the execution of apoptosis in mammalian cells, and activation of caspase 3 is therefore a hallmark of apoptotic cells .
Active caspase 3 proteolytically cleaves and activates, among other targets, PARP involved in DNA repair and DFF40/CAD DNase, the executor of nuclear DNA fragmentation. Apoptotic cells are characterized by cleavage of the native 116-kDa form of PARP into 85-kDa and 25-kDa forms. Concurring with the observed absence of the active form of caspase 3, PARP cleavage was not observed in celecoxib-treated RA FLSs but was observed in those treated with TRAIL (Figure 7c). Moreover, we could not detect DNA fragmentation in RA FLSs treated for either 12 or 24 hours with celecoxib concentrations of 40, 50, or 60 μM, but we could in TRAIL-treated cells (Figure 7d). Taken together, our results suggest that the cell death pathway induced by celecoxib on RA FLSs occurs in a caspase-independent manner.
Apoptosis is a form of cell death in which a programmed sequence of events leads to the elimination of cells without releasing harmful substances into the surrounding area. Apoptosis plays a crucial role in controlling cell numbers by eliminating old cells, unnecessary cells, and unhealthy cells. Deregulation of apoptosis thus can lead to the survival and hyperproliferation of unwanted cells such as FLSs in RA. Therefore, one strategy for treatment is the design of drugs that can restore the normal apoptotic pathways in hyperproliferative cells.
The anti-inflammatory drug celecoxib, an inhibitor of COX-2, was reported by Kusunoki and colleagues  to be pro-apoptotic on RA FLSs. In that study, the viability of synovial cells was reduced by celecoxib in a dose-dependent manner similar to our observation. Kusunoki and colleagues observed that celecoxib strongly reduced cell viability of RA FLSs when used at concentrations of at least 30 μM. The authors concluded that celecoxib induces apoptosis in RA FLSs as they observed a strong DNA fragmentation in RA FLSs treated with 30 μM celecoxib.
We compared the characteristics of celecoxib-induced cell death in RA FLSs with those induced by the established pro-apoptotic factor TRAIL by Annexin V staining/TO-PRO-3 uptake. We have previously reported that 4 hours of co-culturing with TRAIL resulted in apoptosis of approximately 30% of RA FLSs as determined by Annexin V staining/TO-PRO-3 uptake. This technique allows investigators to distinguish early apoptotic cells (Annexin+/TO-PRO-3-) from late apoptotic/necrotic cells (Annexin+/TO-PRO-3+) . Annexin V is a Ca2+-dependent phospholipid-binding protein with high affinity for phospatidylserine and can be used as a sensitive probe for the early phase of apoptosis that is characterized by phospatidylserine exposure on the cell membrane. Because of increased permeability, Annexin V binding can also occur during cell necrosis, and uptake of DNA stain TO-PRO-3 is taken as a parameter to distinguish necrotic, and thus permeable, cells .
Whereas we observed pre-apoptotic cell death in RA FLSs upon 4 hours of TRAIL treatment, pre-apoptotic cells were hardly detectable in celecoxib-treated cells. We exposed RA FLSs to different concentrations of celecoxib for various incubation times, but under none of the tested conditions were pre-apoptotic (that is, Annexin V+ and TO-PRO-3-) cells detectable. Cell death was observed only at concentrations above 40 μM celecoxib (Figure 2), although we detected a decrease in the metabolic activity of FLSs treated with lower concentrations of celecoxib, which is in agreement with Kusunoki and colleagues . We also confirm that celecoxib strongly inhibited RA FLS proliferation, as shown in their study .
It has been suggested that cell death should be classified as apoptosis only if execution of cell death is dependent on caspase activity . We therefore tested whether caspase 3 is activated in celecoxib-treated cells as caspase 3 is a key executor of apoptosis. Whereas the cleaved (thus active) form of caspase 3 was detectable in cell lysates of TRAIL-treated RA FLSs, only the proform of caspase 3 was visible in celecoxib-treated cells. Concurring with this observation, neither a pan-caspase inhibitor nor a specific caspase 3 inhibitor could protect RA FLSs against celecoxib-induced cell death. Similar observations were made with caspase 8 and caspase 9 inhibitors (data not shown). We therefore conclude that celecoxib-induced cell death in RA FLSs is independent of caspases.
These results are in contrast to those of Kusunoki and colleagues , who observed DNA fragmentation in RA FLSs treated for 24 hours with celecoxib and an inhibition of this DNA fragmentation by the addition of caspase 3 inhibitors. A possible explanation for these differences might be the different cell systems used. Kusunoki and colleagues used the first two passages of fibroblasts prepared from synovial tissue for their experimentation. We, however, employed RA FLSs between passages 4 and 10 in order to exclude a contamination of other cell types because approximately 30% of the synovium is composed of macrophage-like synoviocytes.
Moreover, evidence is accumulating that taking DNA fragmentation as the readout of caspase inhibition is not sufficient to conclude the contribution of caspases to cell death . It is therefore possible that the caspase dependency of DNA fragmentation described by Kusunoki and colleagues is a secondary event during celecoxib-induced cell death, which could also explain their observed dose-independent effect of the caspase inhibitors. To conclude an apoptotic cell death, other parameters of cell death such as mitochondrial dysfunction, phosphatidylserine exposure, and plasma membrane permeabilization have to be considered . Nevertheless, DNA fragmentation can also be observed in non-apoptotic cell death pathways, as for example during necrosis .
We conclude from our results that apoptosis is not the major death pathway in RA FLSs induced by high concentrations of celecoxib. This observation is in line with that of a previous report, in which celecoxib was described as being able to induce non-apoptotic cell death in cardiac myocytes . Administration of antioxidants, such as dithiothreitol, N-acteyl-cysteine, or calcium-blocking reagents, did not alter celecoxib-induced cell death, excluding an implication of oxidative stress and intracellular calcium signals (data not shown). The morphological changes together with the rapid membrane permeabilization of RA FLSs during celecoxib treatment suggest rather a necrotic-like cell death. Necrosis, however, leads to the release of inflammatory cellular contents which is unfavorable in the treatment of RA. The proposed local administration of higher celecoxib concentrations in the synovial space of the joint of arthritis patients  must therefore be reconsidered.
= dimethyl sulfoxide
= fetal calf serum
= fibroblast-like synoviocyte
= poly(ADP-ribose) polymerase
= phosphate-buffered saline
= rheumatoid arthritis
= tumor necrosis factor-related apoptosis-inducing ligand
= benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-FMK inhibitor
= benzyloxycarbonyl-Val-Ala-Asp (OMe) fluoromethylketone.
This work was supported by Société Française de Rhumatologie and Pfizer Laboratory (New York, NY, USA). We thank Lourdes Planelles for help with the fluorescence-activated cell sorting analysis, Solange Desagher and Nelly Noraz for critical reading of the manuscript, and Michel Chammas and Bertrand Coulet for providing synovial tissues.
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