Tissue factor as a proinflammatory agent
© BioMed Central Ltd 2002
Received: 21 May 2001
Accepted: 15 October 2001
Published: 10 January 2002
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© BioMed Central Ltd 2002
Received: 21 May 2001
Accepted: 15 October 2001
Published: 10 January 2002
Tissue factor (TF) is a transmembrane glycoprotein and the main triggering element of blood coagulation. TF expression on monocytes and endothelial cells is induced by exposure to endotoxin, tumor necrosis factor, and IL-1 and is considered to appear in consequence of inflammation. In order to assess the proinflammatory capacity of TF itself, the recombinant extracellular domain of TF was injected intra-articularly into healthy mice. To characterize the role of immune cells in the TF-induced arthritis, mice deprived of lymphocytes, neutrophils and monocytes were used. Histomorphological analysis of the joints with respect to inflammatory cell infiltration, pannus formation and erosion formation revealed development of arthritis in 80% of animals injected with TF. In most of the cases synovial proliferation was accompanied by pannus formation and cartilage destruction. Inflammatory cell infiltrate consisted of CD4-Mac1+ macrophages. Depletion of monocytes was, however, not enough to abolish inflammation. Indeed, combined deficiency of monocytes and lymphocytes was required to prevent inflammation following the injection of TF. We observed that TF induced chemokine production (MIP-1α and RANTES), but did not induce a proliferative response nor cytokine release by mouse spleen cells. TF has strong inflammatogenic properties mediated predominantly by monocytes and their release of chemokines. Our study shows that TF can simultaneously trigger the immune and coagulation systems.
Tissue factor (TF) is a transmembrane glycoprotein and the major cellular trigger of blood coagulation. Assembly of a complex between TF and factor VII (FVII) initiates fibrin formation. Besides its role in blood coagulation, TF is also important for the vascular development regulating embryonic angiogenesis and supporting proliferative and invasive capacities of cells [1–4]. Expression of TF on the cell surface and its appearance as a soluble molecule are characteristic features of acute and chronic inflammation in conditions such as sepsis, atherosclerosis, Crohn's desease, systemic lupus erythematosus, and rejection reactions [5–9].
The role of TF in the inflammatory process is a matter of discussion. A variety of inflammatory stimuli, including mitogens, bacterial cell products, components of the complement system and cytokines, are known to promote the expression of TF on the surface of endothelial cells and monocytes . T cells regulate TF expression: upregulation is achieved by Th1 cytokines, while Th2-derived cytokines are mostly inhibitory . TF, in turn, may participate in cellular interactions promoting leukocyte adhesion and transendothelial migration [12, 13].
In the present study we investigated the capacity of TF to induce inflammation by injecting human recombinant TF (rTF) into joint cavities of healthy mice. Histomorphological investigation of the injected joints showed a remarkable cellular infiltration of synovia and occasionally cartilage destruction, indicating that TF possesses strong proinflammatory properties. Expression of TF on monocytes and synovial cells may be crucial for potentiating the initial stages of inflammation in joints.
BALB/c and NMRI mice were purchased from ALAB (Stockholm, Sweden). Severe combined immunodeficient (SCID) mice and their congenic strain CB17 were purchased from M&B (Bomholtvej, Denmark). All mice were housed in the animal facility of the Department of Rheumatology, University of Göteborg. Female mice 6–8 weeks of age were used in all the experiments.
This version of rTF contains the extracellular domain of human TF, amino acid residues 1–219 , which retains the ability to bind to FVII and FVIIa and to enhance enzymatic activity of FVIIa. rTF preparation was dissolved in Hepes buffered saline (Hepes 30 mM, NaCl 100 mM, 0.02% Na-azide; pH7.5) and kept in aliquots at -70°C until use. Two preparations of TF were used that contained 3.7 μg/ml and 32 ng/ml of lipopolysaccharide (LPS), respectively. No significant difference in the results obtained with these two preparations was observed and the results were thus pooled.
NMRI strain mice were used in the experiments unless stated otherwise. Induction of arthritis was performed by injection of rTF in a volume of 20 μl intra-articularly into the right knee joint. Control experiments were performed by injecting an equivalent amount of LPS preparation in Hepes buffered saline into the contralateral knee joint.
Neutrophil depletion was performed by intraperitoneal injection of the monoclonal antibody RB6-8C5 (hybridoma was kindly provided by Dr R Coffman, DNAX Research Institute, Palo Alto, CA, USA) two hours before the rTF injection, as described previously . The IgG rat antiovalbumin monoclonal antibody (kindly provided by Dr E Telemo, Department of Clinical Immunology, University of Göteborg, Sweden) was injected into the control group. Monocyte depletion was induced by subcutaneous injection of etoposide (Bristol-Myers Squibb, Bromma, Sweden; 12.5 mg/kg body weight, in a volume of 100 μl ) on three consecutive days before and three consecutive days after injection of rTF. The impact of lymphocytes was studied by injecting rTF into SCID mice lacking B and T lymphocytes and their congenic strain, CB17.
This was achieved by using mini-osmotic pumps (model 2002, Alza Corp, Palo Alto, CA, USA) filled with buffered solution containing 200 U/ml ancrod (Sigma Chemical, St Louis, MO, USA) implanted subcutaneously three days before the injection of rTF .
Histological examination of joints was done after paraffin embedding, cutting, and staining with hematoxylin and eosin. All the slides were coded and evaluated blindly. The specimens were evaluated with respect to occurrence of synovial hypertrophy, inflammatory cells in synovial sublining compartment, pannus formation and cartilage and/or subchondral bone destruction. Intensity of synovial inflammation (arthritis index) was graded arbitrarily from 0 to 3.
For immunohistochemical examination, the knee joints were removed and demineralized as described . Serial cryosections of 6 μm thickness were stained with rat monoclonal antibodies directed against mouse CD11b (Mac-1; M 1/70) or CD4 (GK1.5) (both antibodies from PharMingen, San Diego, CA, USA), then incubated with biotinylated secondary antibodies (DAKO A/S, Gosulp, Denmark) and avidin-biotin-peroxidase complexes (ABC). All sections were counterstained with Mayer's hematoxylin.
Murine splenocyte suspension (cell density 2 × 106/ml) in Iscove's medium supplemented with 10% fetal calf serum (FCS), 2 nM L-glutamine, mercaptoethanol and 50 μg/ml gentamicin was stimulated with rTF at a final concentration of 0.1–10 μg/ml. At defined time points, supernatants were collected for determination of cytokine and chemokine levels.
Proliferation was determined by the incorporation of [3H]-thymidine (specific activity, 42 Ci/mmol; Amersham International, Buckinghamshire, UK) into splenocyte suspension (cell density 4 × 105/ml), stimulated for 72 hours with either rTF or LPS at a final concentration of 0.1–10 μg/ml. The results were expressed as a stimulation index (counts per minute, mean ± standard deviation).
The level of interleukin (IL)-6 in the rTF-stimulated supernatants was determined by a bioassay measuring the effect of test samples on the growth of the IL-6-dependent cell line B13.29 . The results were analyzed by incorporation of [3H]-thymidine after 72 hours stimulation and compared to results with the standard dilutions of recombinant mouse IL-6 (Genzyme, Cambridge, MA, USA).
The levels of macrophage inflammatory protein (MIP)-1α and RANTES (regulated on activation normal T-cell expressed and secreted) were measured by an enzyme-linked immunosorbent assay using Quantikine M kits (R&D Systems, Minneapolis, MN, USA) and expressed in pg/ml.
The differences in the incidence and the severity of arthritis in the groups were analyzed by the Fisher's test and Mann–Whitney U test, respectively.
The ability of rTF to induce arthritis was evaluated by injection of rTF in the doses 0.2, 2.0, and 20 μg (0.004, 0.04, and 0.4 nmol) into the knee joint of NMRI mice. Four days after the inoculation, morphological signs of arthritis (synovial tissue hypertrophy, and inflammatory cell infiltrates) were found in 33%, 56% and 83% of joints, respectively. Control mice injected with the amount of LPS equivalent to its concentration in the rTF preparation exhibited arthritis only in 28% of cases (13/15 versus 4/14; P < 0.01). The arthritis index of the rTF-induced arthritis was significantly higher in joints injected with 20 μg of rTF than in the controls (1.73 versus 0.23; P < 0.01). Moreover, 6/13 joints injected with 20 μg of rTF developed extrasynovial features of arthritis (pannus formation, n = 2; cartilage destruction, n = 3 and periarticular bone destruction, n = 1) compared to only one in the control group. In all further experiments the dose of 20 μg of TF per knee was used.
Sensitivity to rTF varied between the healthy mouse strains. Four days after the injection of rTF (20 μg/knee) into NMRI (n = 15), CB17 (n = 8) and BALB/c mice (n = 8), morphological signs of arthritis were registered in 80%, 75% and 50% of knee joints, respectively. These results indicate that susceptibility to inflammatory potential of rTF is dependent on genetic background of the host.
Systemic depletion of fibrinogen with ancrod prior to rTF injection did not reduce the incidence of rTF-induced arthritis in 6/8 NMRI mice.
Effects of rTF on lymphoid cells were investigated by incubating mouse splenocytes with rTF (0.1 μg/ml, 1 μg/ml, 5 μg/ml, or 10 μg/ml). Investigation of supernatants after 48 hours of stimulation for the level of IL-6, RANTES, and MIP-1α demonstrated a dose-dependent increase in the level of chemokines. The increase was pronounced for MIP-1α (73 ± 33 pg/ml in non-stimulated cells versus 139 ± 32 pg/ml after stimulation with 5 μg/ml of rTF; n = 3) but was only marginal for RANTES (256 ± 46 pg/ml versus 365 ± 32 pg/ml; n = 3). In contrast, neither change in the level of IL-6 nor proliferation of lymphocytes was observed.
Inflammation and thrombosis are linked in many clinical conditions. It is presumed that proinflammatory mediators potentiate activation of blood coagulation and serine proteases of the coagulation system, especially the terminal enzyme thrombin, known for proinflammatory and mitogenic/chemotactic effects both in circulation and locally in synovial tissue [20–22]. An indication of the importance of TF in the inflammatory process was obtained in the animal model of sepsis, in which TF-dependent procoagulant activity correlated with the level of tumor necrosis factor-α . In addition, modulation of TF-dependent coagulation by administration of either TF-pathway inhibitor or anti-TF antibodies decreased circulating levels of IL-6 and IL-8 [24, 25], and diminished proliferation and perivascular cell infiltration [26, 27]. This study shows that the TF molecule possesses strong proinflammatory properties, causing arthritis. Histological analysis revealed that TF-induced synovitis could be attributed mostly to infiltrating macrophages. Mononuclear cell influx into synovia is an early finding in the majority of asymptomatic subjects, preceding clinically overt arthritis in RA [28, 29]. Furthermore, synovial macrophage infiltration is a characteristic feature of both autoimmune and bacterial arthritis [30, 31] and is a determinant of joint erosions [32, 33]. Our observation, in combination with an increased TF-dependent procoagulant activity in blood and synovial fluid of patients with RA, implies participation of TF in triggering the initial steps of inflammation during RA and/or in rendering the inflammation chronic.
Composition of inflammatory infiltrate and cell depletion studies showed that TF exerts its proinflammatory properties in a cell-specific manner targeting the macrophage/ monocyte population. This is not surprising taking into consideration that macrophages/monocytes are the only cells in the blood circulation compartment which express TF on their surface [8, 34]. Moreover, we demonstrated that an interaction between monocytes and lymphocytes was a prerequisite of the TF-induced arthritis. Activated T cells were able to induce TF production by stimulating monocytes through CD40 ligand [35, 36]. This mechanism may contribute to a positive feedback essential for maintenance of TF-induced inflammation. Interestingly, neutrophils, other principal inflammatory cells, were not sensitive to TF stimulation – these cells were neither found in synovial tissues nor affected arthritis frequency in the depletion experiments.
Mononuclear cells composing the inflammatory infiltrate in synovia were mostly Mac-1+ CD4- cells. Abundant expression of Mac-1 molecule on the monocyte surface indicates a principal role of β2-integrins in cell activation following exposure to TF. Two methods of such activation may be considered. TF may attract Mac-1+ cells indirectly by increasing formation of coagulation proteins known as Mac-1 ligands, e.g. Factor X and fibrinogen. However, the high incidence of TF-induced arthritis in defibrinated mice favors a direct stimulatory effect of TF on sensitive cells. Treatment of macrophages with TF in vitro has been shown to increase the expression of β2-chain-containing adhesion molecules  and supports the idea of direct TF-induced Mac-1 expression. Lack of CD4+ cells responsible for peptide presentation through MHC class II molecules shows that this mechanism is not compulsory for TF-induced synovial infiltration, in contrast to experimental glomerulonephritis where simultaneous expression of TF and MHC class II molecules was observed and efficiently blocked by anti-TF antibodies [38, 39].
The way in which TF interacts with macrophages is not clear. Exposure of spleen cell cultures to TF did not induce the release of proinflammatory cytokines. These results favor the suggestion that TF acts directly on inflammatory cells and not by a cytokine-mediated mechanism. TF-mediated release of chemoattractant molecules, which recruit inflammatory cells from the circulation or surrounding tissues, is an alternative possibility. We found that in vitro splenocyte stimulation with TF was associated with selective release of the monocyte chemoattractant molecule MIP-1α. This observation may explain the dominance of mononuclear cells in the synovial inflammatory infiltrates of the joints injected with TF.
Altogether our observations suggest that TF may play an active role during arthritis by direct and/or indirect stimulation of influx of monocytes into the synovial tissue.
fetal calf serum
macrophage inhibitory protein
regulated on activation normal T-cell expressed and secreted
severe combined immunodeficient
The study was approved by the Ethics Committee of Sahlgrenska Hospital and animal experimentation guidelines were followed. The work was supported by the Göteborg Medical Society, the Swedish Association against Rheumatism, the King Gustaf V's Foundation, the Swedish Medical Research Council, the Nanna Svartz' Foundation, National Inflammation Network and the University of Göteborg.