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(American Journal of Pathology. 2003;162:943-951.)
© 2003 American Society for Investigative Pathology

Short-Term Exposure of Cartilage to Blood Results in Chondrocyte Apoptosis

Michel Hooiveld^*, Goris Roosendaal, Marion Wenting^*, Marijke van den Berg, Johannes Bijlsma^* and Floris Lafeber^*

From the Department of Rheumatology and Clinical Immunology^* and the Van Creveldkliniek (National Hemophilia Center), University Medical Center Utrecht, Utrecht, The Netherlands

	Abstract

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Studies have shown that joint bleeding leads to cartilage degradation independent of concurrent synovitis. We hypothesized that the blood-induced cartilage damage is because of increased chondrocyte apoptosis after short-term exposure of whole blood or isolated mononuclear cells plus red blood cells to cartilage. Human cartilage tissue samples were co-cultured for 4 days with whole blood (50% v/v) or with mononuclear cells plus red blood cells (50% v/v equivalents). Cartilage matrix proteoglycan synthesis (³⁵SO₄^2- incorporation) was determined after 4 days as well as at day 16 (after a 12-day recovery period in the absence of any additions). To test the involvement of apoptosis a specific caspase-3 inhibitor (acDEVDcho, 0 to 500 µmol/L) as well as a pan-caspase inhibitor (zVADfmk, 0 to 500 µmol/L) were added. Chondrocyte apoptosis was evaluated by immunohistochemical staining of single-strand DNA and by terminal dUTP nick-end labeling. Cartilage co-cultured with whole blood as well as mononuclear cells plus red blood cells induced a long-term inhibition of proteoglycan synthesis (74% and 78% inhibition on day 16, respectively). Immunohistochemistry showed a threefold increase in apoptotic chondrocytes in cultures with 50% whole blood as well as with mononuclear cells plus red blood cells. Both the specific caspase-3 inhibitor and the pan-caspase inhibitor partially restored proteoglycan synthesis in the cartilage after blood exposure. This effect was accompanied by a decrease in the number of apoptotic chondrocytes. These data suggest that a single joint hemorrhage (a 4-day exposure of cartilage to 50% v/v blood) results in induction of chondrocyte apoptosis, responsible for the observed inability of the chondrocytes to restore the proteoglycan synthesis during recovery from a short-term exposure to blood. This reduced restoration could eventually lead to cartilage degeneration and ultimately joint destruction.

Currently little is known about the pathogenesis of this blood-induced cartilage damage, although several mechanisms have been proposed. It has been suggested that accumulation of iron from red blood cells (RBCs), ie, hemosiderine, in synovial tissue results in the production of proteolytic enzymes. Also the production of proinflammatory cytokines released by synoviocytes and recruited phagocytes are thought to be primarily responsible for cartilage damage and joint destruction.^6,7 However, it became clear that, although these processes do contribute significantly to joint damage after repeated bleeding as in hemophilia, they are not the first to occur.^2-4

We showed that a short intra-articular bleeding episode in vivo or a short exposure of cartilage to blood in vitro induces lasting degenerative changes in cartilage independent of synovial inflammation and proinflammatory cytokine production.^4,8 Synthesis and release of matrix components such as proteoglycans are inhibited by blood in a concentration-dependent manner. It seems that these changes are the result of the combined presence of mononuclear cells (MNCs) and RBCs, whereas both cell types individually do not result in lasting changes.^3,8 The changes in cartilage after a relatively short exposure to blood were degenerative in nature and showed similarities to osteoarthritis, ie, a centrifugal pattern of cartilage damage, loss of cartilage matrix components, as well as chondrocyte clustering.² Although primarily degenerative in nature, the exact mechanisms behind the induction of these long-lasting alterations in chondrocyte activity and cartilage damage are not yet understood.

Apoptosis in chondrocytes has been shown to adversely affect cartilage matrix turnover and chondrocyte apoptosis is associated with osteoarthritis.^9-11 Similar adverse degenerative changes in cartilage matrix turnover are also observed after blood exposure. This suggests chondrocyte apoptosis might be involved in the prolonged disturbed cartilage matrix turnover after joint hemorrhage.

Therefore we evaluated the hypothesis that exposure of cartilage to blood results within days in chondrocyte apoptosis, without the interference of synovial inflammation. We tested this in an in vitro co-culture system of human cartilage with blood.

	Materials and Methods

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Cartilage Culture Technique

Healthy full-thickness articular cartilage tissue was obtained postmortem from human humoral heads within 24 hours after death of the donor. The donors (n = 18; mean age, 69.8 ± 14.3 years; 12 males and 6 females) had no known history of joint disorders. Macroscopic analysis revealed completely intact articular cartilage that previously has been shown to represent healthy cartilage.¹² When histology was performed in our experiments (see below), data corroborated that the cartilage used was intact and healthy. Slices of cartilage were cut aseptically from the articular surface, excluding the underlying bone, and kept in phosphate-buffered saline (PBS, pH 7.4). Cartilage was treated and handled as described.¹² Briefly, within 1 hour of dissection the slices were cut into square pieces and weighed aseptically (range, 5.0 to 15.0 mg) and each sample was individually put into culture in 96-well round-bottom microtiter plates (200 µl of culture medium, 5% CO₂ in air, 37°C, pH 7.4). The culture medium consisted of Dulbecco’s modified Eagle’s medium supplemented with glutamine (2 mmol/L), penicillin (100 IU/ml), streptomycin sulfate (100 µg/ml), ascorbic acid (85 µmol/L), and 10% heat-inactivated pooled human male AB⁺ serum.

Preparation of Blood (Components)

For each individual experiment fresh blood from healthy donors (n = 12; mean age, 30.0 ± 7.1 years; six males and six females) was collected into heparinized vacutainer tubes (143 USP Li-heparin/10 ml, Becton Dickinson). To obtain a concentration of 50% v/v whole blood was diluted in culture medium.

MNCs were isolated by density centrifugation, using Ficoll-Paque (Pharmacia, Uppsala, Sweden), and washed twice in ice-cold Dulbecco’s modified Eagle’s medium. RBCs of the same donor were isolated by filtration (PALL, The Netherlands). MNCs and RBCs were redistributed in culture medium to their original cell number before isolation, based on cell counts before and after isolation (Coulter Counter). The amounts of cells used are equivalent to a concentration of 50% v/v whole blood, which previously has been proven to evoke the same lasting changes in cartilage matrix turnover.³

Experimental Design

Cartilage samples were cultured, without a preculture period, for 4 days in the presence of whole blood or MNCs plus RBCs, with or without additions. Inhibition of proteoglycan synthesis was determined as a measure of inhibition of cartilage matrix synthesis. To measure the reversibility of the inhibition, after a 4-day exposure, the cartilage was washed twice (200 µl of culture medium, 45 minutes, under culture conditions) and cultured for an additional 12 days (referred to as recovery period) in the absence of blood cells. The culture medium was changed every 4 days. On both days, day 4 and 16, proteoglycan synthesis was measured. In addition, cartilage samples after 4 and 16 days of culture were fixed in methanol/PBS (6:1) and used for immunohistochemical detection of apoptosis. For each experiment a separate cartilage donor and blood donor was used, the n values represent the number of these experiments.

Proteoglycan Synthesis Inhibition

Proteoglycan synthesis was measured as the rate of sulfate incorporation during the last 4 hours of the 4- and 16-day culture period. At the end of both time points Na₂³⁵SO₄ (37 MBq/ml, NEX-041-H, carrier-free; DuPont, The Netherlands) was used as a tracer and added in 10-µl aliquots (74 kBq) to the 200 µl of culture medium. In the case of the 4-day culture, cartilage samples were placed in fresh medium before addition of ³⁵SO₄^2- without blood or isolated cells (to prevent interference of the blood cells with the incorporation rate). Procedures were followed as described previously.¹³ In short, after 4 hours, the tissue samples were rinsed twice in ice-cold PBS, digested with 2% papain (Sigma, The Netherlands), and the glycosaminoglycans were precipitated with cetylpyridinium chloride (Sigma). The amount of ³⁵SO₄^2- incorporated was analyzed by liquid scintillation analysis. The ³⁵SO₄^2- incorporation rate was normalized to the specific activity of the medium and is expressed as nmol of sulfate incorporated per hour per gram wet weight of cartilage tissue.

Interleukin (IL)-1ß and Tumor Necrosis Factor (TNF)- Production

Supernatants from control cartilage and cartilage co-cultured with whole blood or MNCs plus RBCs were harvested and rendered cell-free by centrifugation (500 x g, 10 minutes). Concentrations of IL-1ß and TNF- were measured by using an enzyme-linked immunosorbent assay according to the manufacturer’s instructions (Medgenix, The Netherlands). Detection limits were 20 pg/ml for both IL-1ß and TNF-.

Apoptosis Induction

The role of chondrocyte apoptosis during co-culture of cartilage with whole blood or MNCs plus RBCs was investigated by addition of caspase inhibitors. acDEVDcho (0 to 500 µmol/L; BioSource), a caspase-3-specific inhibitor, and zVADfmk (0 to 500 µmol/L; Enzyme Systems Products), a pan-caspase inhibitor, were added during the first 4 days of culture when whole blood or MNCs plus RBCs were present. As a positive control, and to compare the effects of apoptosis on the proteoglycan synthesis, cartilage samples were incubated during the first 4 days of culture with the apoptogen staurosporine (10 µmol/L; BioMol).¹⁴

For immunohistochemical detection of apoptotic chondrocytes, human cartilage samples harvested after 4 and 16 days of (co)culture, were fixed in methanol/PBS (6:1) for 3 days at -20°C. Fixed samples were dehydrated with absolute methanol, prepared with xylene, and embedded in paraffin. Sections (4 µm) were cut and deparaffinized. Apoptotic chondrocytes were either detected with anti-single-strand DNA monoclonal antibody (clone F7–26/apostain; Alexis Corporation, The Netherlands) or by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL; Roche, Germany). Both techniques had hematoxylin counterstaining to detect total DNA content at the chondrocyte locations. The amount of red-positive cells was calculated as a percentage of the total amount of chondrocytes per slice, excluding empty lacunae.

The histological sections used for ssDNA staining were prepared as described before.¹⁵ Briefly, cartilage sections were rehydrated in PBS, followed by incubation with PBS (with 5 mmol/L of MgCl₂) containing 0.2% Triton X-100 for 5 minutes. After transfer of the slides in plastic tubes containing PBS supplemented with 5 mmol/L of MgCl₂, the slides were heated in a water bath at 99°C for 7 minutes to denature unstable DNA. Immediately after heating, the sections were placed in tubes containing ice-cold PBS. The sections were incubated with the anti-ssDNA monoclonal antibody and stained with alkaline phosphatase conversion.

For the TUNEL assay slices were rehydrated in PBS and slides were placed in 200 ml of 0.1 mol/L citrate buffer (pH 6), heated in a microwave oven (750 W, 1 minute) and rapidly cooled by immediately adding 80 ml of distilled water (room temperature). Slides were transferred in PBS and preincubated with 3% bovine serum albumin/Tris-HCl (pH 7.5) and normal bovine serum (20% v/v). Then slides were rinsed with PBS at room temperature and TUNEL mixture was applied during 1 hour, subsequently sheep anti-fluorescein isothiocyanate-alkaline phosphatase antibody was added, which converted alkaline phosphatase-substrate into red detectable spots.

Chondrocyte Apoptosis and Inhibition of Proteoglycan Synthesis

In a separate set of experiments the effect of both caspase inhibitors was tested on cartilage explants exposed to blood and MNCs plus RBCs, quantifying in the same experiment apoptosis and inhibition of proteoglycan synthesis. Conditions and techniques were identical as described above. The concentrations of acDEVDcho and zVADfmk were 500 µmol/L.

Calculations and Statistical Analyses

Each experiment in which proteoglycan synthesis was measured was performed with cartilage of a single donor with at least 10 tissue samples for each culture condition, each taken at random and handled individually. The mean value of the 10 explants was taken as representative for that condition per experiment. For the co-cultures of cartilage with MNCs plus RBCs repeated experiments were performed with cartilage and blood cells of three different donors of which mean values (±SEM) are given. Previous experiments have shown that the effects of these MNCs plus RBCs are similar to that of whole blood. Nevertheless, co-cultures of cartilage with whole blood were performed to verify the effects of the isolated MNCs plus RBCs. For these cultures averages of the 10 cartilage samples of a single experiment with intra-assay variation (±SEM) are given.

For histological examinations, four slices of eight consecutive slices, taken at approximately a quarter of the edge of each tissue sample, were scored by two independent observers blind to the culture condition of the cartilage. Of each culture condition from each cartilage donor the average values were considered representative for that experiment and used for statistical calculation. Experiments were performed with cartilage and blood cells of three separate donors. Mean values of these three experiments (±SEM) are given.

For the combination experiments (the effects of caspase inhibitors on proteoglycan synthesis and number of apoptotic cells) identical procedures and calculations were used. Mean values (±SEM) for four analyses using cartilage of two different donors are given.

Differences between treatments were statistically analyzed using a nonparametric test for independent samples (Mann-Whitney), using SPSS v9.0 software. P values 0.05 were considered statistically significant.

	Results

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Inhibition of Proteoglycan Synthesis and Reversibility of This Effect

Proteoglycan synthesis was almost completely inhibited after a 4-day in vitro exposure of cartilage to 50% v/v whole blood or equal amounts of isolated MNCs plus RBCs (Figure 1) . This inhibition of proteoglycan synthesis was still evident (>78% inhibition) after 12 days of recovery (day 16). No significant differences were found between the effects of whole blood and the addition of MNCs plus RBCs added in equivalent amounts as present in whole blood (Figure 1) . Previous experiments have shown that the addition of the plasma (equivalents of 50% whole blood) or up to 50% serum, did not influence cartilage matrix turnover in any way.³

View larger version (23K): [in this window] [in a new window]   Figure 1. Inhibition of proteoglycan synthesis by whole blood or the combination of MNCs plus RBCs. Sulfate incorporation was used as a measure of proteoglycan synthesis in cartilage. Mean values ± SEM (n = 3 experiments, P < 0.05). Open bars represent the proteoglycan synthesis after 4 days of either controls, co-cultures with 50% whole blood, or MNCs plus RBCs. The figure shows that there is 92% inhibition of proteoglycan synthesis compared to the control synthesis (*, P < 0.05). Shaded bars represent the proteoglycan synthesis after 12 days of additional culture without additions to determine recovery of synthesis by chondrocytes. Proteoglycan synthesis was for both the 50% whole blood and MNC plus RBC co-cultures significantly inhibited (up to 78%; *, P < 0.05). No significant differences in proteoglycan synthesis were found between co-cultures with 50% whole blood and MNCs and RBCs on both days 4 and day 16 (n.s.).

The Role of IL-1ß and TNF-

IL-1ß and TNF- are the most important inflammatory mediators in cartilage destruction. The levels of these cytokines, to establish their role in the induction of prolonged inhibition of proteoglycan synthesis after blood exposure, were measured in supernatants of the co-cultures. Slightly enhanced levels of both proinflammatory cytokines were found at day 4 (Table 1) . After washing and subsequent culture in the absence of additions, cytokine levels at day 16 were below detection levels. The levels observed after 4 days are known to reduce proteoglycan synthesis. However, these levels have been reported not to be able to induce prolonged irreversible inhibition of proteoglycan synthesis.^8,16,17 Addition of similar amounts of IL-1ß and TNF- as measured on blood cell addition results in comparable inhibition of proteoglycan synthesis. Refreshment of medium, and thus removing the cytokines, results in complete normalization of proteoglycan synthesis (data not shown).

View this table: [in this window] [in a new window]   Table 1. Levels of Proinflammatory Cytokines IL-1ß and TNF- in Supernatant of Co-Cultures of MNCs Plus RBCs or 50% Whole Blood with Human Cartilage

Cartilage cultured in the presence of the apoptogen staurosporine during the first 4 days showed a concentration-dependent inhibition of proteoglycan synthesis (data not shown). At a concentration of 10 µmol/L, staurosporine could inhibit proteoglycan synthesis equal to 4 days of co-culture with whole blood or MNCs plus RBCs. A subsequent culture of 12 days without staurosporine demonstrated lasting inhibition of proteoglycan synthesis (Figure 2) .

View larger version (20K): [in this window] [in a new window]   Figure 2. Inhibition of proteoglycan synthesis after induction of apoptosis through addition of staurosporine (STS). Sulfate incorporation was used as a measure of proteoglycan synthesis in cartilage. The open bars represent the synthesis after 4 days of cartilage culture, in the absence or presence of staurosporine (STS, 10 µmol/L). Shaded bars represent the proteoglycan synthesis in cartilage cultured for an additional 12 days without additions to determine the recovery of synthesis by chondrocytes. Cartilage cultured with STS showed an irreversible 92% inhibition of proteoglycan synthesis through induction of apoptosis (n = 3 experiments; *, P < 0.05).

View larger version (18K): [in this window] [in a new window]   Figure 3. A: Reversibility of the proteoglycan synthesis by preventing apoptosis with acDEVDcho, a caspase-3 inhibitor. The relative sulfate incorporation compared to control cultures (percent of control synthesis ± SEM) is shown. Cartilage samples were co-cultured in the presence of MNCs plus RBCs and acDEVDcho (0 to 500 µmol/L). Open bars show the absence of an effect of acDEVDcho on day 4. Hatched bars show the statistically significant recovery of proteoglycan synthesis on day 16 with increasing concentrations of acDEVDcho (up to 39% of control synthesis, n = 3 experiments; *, P < 0.05). B: Reversibility of the proteoglycan synthesis in cartilage after exposure to 50% whole blood by preventing chondrocyte apoptosis with acDEVDcho, a caspase-3 inhibitor. The relative sulfate incorporation compared to control culture (percent of control synthesis ± SEM) is shown. Cartilage samples were co-cultured in the presence of 50% whole blood and acDEVDcho (500 µmol/L). The open bars show the absence of an effect of acDEVDcho on day 4. Hatched bars show the statistically significant recovery of proteoglycan synthesis on day 16 (up to 51% of control synthesis; *, P < 0.05).

View larger version (22K): [in this window] [in a new window]   Figure 4. A: Reversibility of the proteoglycan synthesis by preventing apoptosis with zVADfmk, a pan-caspase inhibitor. The relative sulfate incorporation compared to control cultures (percent of control synthesis ± SEM) is shown. Cartilage samples were co-cultured in the presence of MNCs plus RBCs and zVADfmk (0 to 500 µmol/L). Open bars show the absence of an effect of zVADfmk on day 4. Hatched bars show the statistically significant recovery of proteoglycan synthesis on day 16 with increasing concentrations of zVADfmk (up to 78% of control synthesis, n = 3 experiments; *, P < 0.05). B: Reversibility of the proteoglycan synthesis in cartilage after exposure to 50% whole blood by preventing chondrocyte apoptosis with zVADfmk, a pan-caspase inhibitor. The relative sulfate incorporation compared to control culture (percent of control synthesis ± SEM) is shown. Cartilage samples were co-cultured in the presence of 50% whole blood and zVADfmk (500 µmol/L). The open bars show the absence of an effect of zVADfmk on day 4. Hatched bars show the statistically significant recovery of proteoglycan synthesis on day 16 (up to 83% of control synthesis; *, P < 0.05).

Blood Exposure Induced Chondrocyte Apoptosis

Immunohistochemical staining of cartilage after a 4-day exposure to MNCs plus RBCs or whole blood with the anti-ssDNA monoclonal antibody as an early marker of apoptosis revealed a significant increase of apoptotic chondrocytes after 4 days of co-culture (Table 2) . Apoptosis was equally distributed throughout the entire cartilage sample. After 12 days of recovery, the number of ssDNA-positive cells observed were not statistically significantly different between the control cultures and the blood-exposed cartilage anymore. As shown in Figure 5A , slices of control cartilage from a 4-day culture period showed hematoxylin staining and very little staining of ssDNA. When cartilage was co-cultured during 4 days in the presence of 50% v/v whole blood or MNCs plus RBCs (50% equivalents of whole blood) the cartilage slices showed a twofold to threefold increase in apoptotic ssDNA-positive cells (Table 2 ; both P < 0.05 and illustrated by Figure 5, B and C , respectively).

View larger version (107K): [in this window] [in a new window]   Figure 5. Representative micrographs of immunohistologically stained human cartilage tissue (original magnifications, x200). The left panels show representatives of cartilage stained for ssDNA after 4 days of co-culture, the right panels are stained with TUNEL after 12 days of recovery period without any additions to the culture medium. A: Control cartilage after 4 days of culture without blood or isolated blood cells. B: Increased staining for ssDNA directly after co-culture of human cartilage with 50% whole blood (day 4). C: Increased staining for ssDNA directly after co-culture of human cartilage with MNCs plus RBCs (day 4). D: Control cartilage stained by TUNEL after a 12-day recovery period showing no apoptotic chondrocytes. E: Increased staining by TUNEL after 12 days of recovery of human cartilage that was co-cultured for 4 days with 50% whole blood. F: Increased staining by TUNEL after 12 days of recovery of human cartilage that was co-cultured for 4 days with MNCs plus RBCs. For average values of several experiments see Table 2 .

Chondrocyte Apoptosis Inhibits Proteoglycan Synthesis

When in the same experiment proteoglycan synthesis and chondrocyte apoptosis were measured, similar results as for the separated experiments were observed (Table 3) . A strong inhibition in proteoglycan synthesis induced by MNCs plus RBCs or by blood (Table 3 , left column) was accompanied by a significant increase in the percentage of apoptotic cells as measured by ssDNA and TUNEL staining at day 4. After a 12-day recovery period proteoglycan synthesis was still significantly inhibited and chondrocyte apoptosis still evident as measured by TUNEL staining. However, the number of ssDNA-stained cells observed was not statistically significant different from controls anymore (Table 3 , ssDNA, day 16; see also Table 2 ). When the caspase inhibitors (DEVD or zVAD) were added during exposure to blood or MNCs plus RBCs, proteoglycan synthesis could partly be restored during the successive 12-day recovery period. Because inhibition of proteoglycan synthesis by cytokines is present during the first 4 days of culture no significant effects of the caspase inhibitors on day 4 were observed. However, the ability to regain matrix synthesis was accompanied by a significantly lower percentage of ssDNA- or TUNEL-positive chondrocytes at day 4 and still evident at day 16 when measured by TUNEL staining (Table 3 , right column). Effects in this respect were not different between MNC plus RBC-exposed cartilage or whole blood-exposed cartilage.

	Discussion

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It has previously been shown that the combination of MNCs plus RBCs, as present in whole blood, is responsible for the effect as observed for whole blood.³ The present results confirm these findings. By what mechanism these two cell populations influence chondrocyte activity, however, is unknown and is subject of this study.

It was hypothesized that the permanent loss of chondrocyte activity as a result of blood or MNC plus RBC exposure is the result of chondrocyte apoptosis. When chondrocytes enter apoptosis, cartilage matrix turnover and possible repair activity on damage is impaired. This will inevitably lead to a disturbed integrity of the cartilage matrix and ultimately results in degradation of cartilage as seen in osteoarthritis.^2,11,14

Our in vitro results show that when cartilage is co-cultured with whole blood or isolated MNCs plus RBCs proteoglycan synthesis is inhibited. Similar inhibition is found when cartilage is incubated with staurosporine, which is a direct stimulus to the induction of chondrocyte apoptosis.^18,19 Staurosporine is a protein kinase inhibitor that which ultimately prevents the action of topoisomerase II and hence induces permanent DNA defects.²⁰

When the specific caspase-3 inhibitory peptide, acDEVDcho, was added during a 4-day co-culture of cartilage tissue with whole blood or MNCs plus RBCs, the cartilage proteoglycan synthesis as measured after 12 days of recovery, could partially be restored. This effect was even more pronounced when the nonselective caspase inhibitor zVADfmk was used, suggesting a protective effect on chondrocytes by preventing apoptosis and with that increased survival rate of chondrocytes. The fact that zVADfmk is more effective than the specific caspase-3 inhibitory peptide acDEVDcho may be because of the fact that zVADfmk acts more upstream in the caspase cascade (ie, caspase-8 and -9), thereby preventing broad activation of the caspase cascade. By preventing the activation of upstream caspases, zVADfmk also prevents the activation of procaspase-3 into caspase-3.²¹

These biochemical data suggest chondrocyte apoptosis after blood exposure, which is confirmed by immunohistochemical staining with ssDNA monoclonal antibody and TUNEL staining. Single-strand DNA staining, namely DNA instability, was found shortly after blood exposure (day 4). At day 16 the effect of blood exposure was not represented by an increase in number of ssDNA-positive cells anymore. There was only a culture-induced increase in early apoptotic cells as observed in the control samples. The TUNEL assay on the other hand was able to detect DNA damage, namely DNA strand breaks, after 12 days of recovery (day 16), and was significantly enhanced in the blood and MNC plus RBC-exposed samples.

Interestingly, at day 4, adding caspase inhibitors could not prevent proteoglycan synthesis inhibition. At day 4 the apoptosis was already evident as observed by immunohistochemical staining. This suggests an additional pathway involved in the primary inhibition of proteoglycan synthesis after blood exposure, as observed at day 4. Despite prevention of apoptosis by caspase inhibitors, there are still increased levels of proinflammatory cytokines, ie, IL-1ß and TNF-, produced in the culture system during the first 4 days of co-culture. It is known that IL-1ß and TNF- can inhibit cartilage matrix synthesis at very low concentrations (<100 pg/ml).^22,23 However, it is described that the levels of IL-1ß and TNF- as measured in our co-culture system do not lead to lasting adverse changes, ie, permanent inhibition of cartilage matrix synthesis during 4 days of culture.^8,16,17,24 This implicates that production of both cytokines, to concentrations reached in our co-culture system, does not lead to apoptosis of chondrocytes, which is consistent with other studies.²⁵ It does not rule out the possibility that IL-1ß and TNF- lead to breakdown of cartilage matrix, but it shows that these cytokines do not induce permanent loss of chondrocyte activity as observed after a 12-day recovery period on a 4-day exposure to blood. The fact that addition of caspase inhibitors prevents the increase in numbers of apoptotic chondrocytes, accompanied by a recovery of proteoglycan synthesis inhibition, strongly suggests the association between apoptosis and persisting inhibition of cartilage matrix synthesis.

These data do suggest that apoptosis plays an important role in the pathophysiology of blood-induced cartilage damage, however, the follow-up is only 16 days. But because of the observed apoptosis and the low or absent proliferation of chondrocytes in adult articular cartilage, it is to be expected that the inhibition of proteoglycan synthesis is long-lasting.²⁶ In time, it could be that the remaining chondrocytes take over the synthetic activity of the lost chondrocytes. If so, this could result in normalization of proteoglycan synthesis. But even then the potency of cartilage repair will remain impaired, unless chondrocyte proliferation takes place.

Reconsideration of therapeutic interventions for intra-articular bleeding in hemophiliacs may be indicated.^27,28 The present data suggest that new treatment strategies to prevent joint destruction may be directed toward prevention of apoptosis. The use of nonselective caspase inhibitors might be an approach in this respect. In an in vivo experimental animal model for myocardial infarct such a strategy, ie, the use of nonselective caspase inhibitors, has been demonstrated to reduce the infarct size.²⁹ This finding might initiate studies to the effectiveness of treatment strategies with caspase inhibitors, treating blood-induced joint damage in an in vivo experimental setting as well.

In conclusion, apoptosis occurs in chondrocytes in vitro after a 4-day exposure to 50% whole blood or an equivalent amount of MNCs plus RBCs. This would imply that the induction of apoptosis in vivo after a single bleeding episode impairs cartilage repair activity and thus will contribute to cartilage damage in time.

	Footnotes

 
Address reprint requests to F. P. J. G. Lafeber, Rheumatology and Clinical Immunology, F02.127, University Medical Center Utrecht, PO Box 85500, 3508 GA Utrecht, The Netherlands. E-mail: f.lafeber{at}azu.nl

Supported by a grant from Aventis Behring.

Accepted for publication December 10, 2002.

	References

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