Arthritis is associated with T-cell-induced upregulation of Toll-like receptor 3 on synovial fibroblasts
- Wenhua Zhu†1, 2,
- Liesu Meng†1, 2,
- Congshan Jiang1, 2,
- Xiaojing He1, 2,
- Weikun Hou1, 2,
- Peng Xu3,
- Heng Du4,
- Rikard Holmdahl5 and
- Shemin Lu1, 2, 6Email author
© Zhu et al.; licensee BioMed Central Ltd. 2011
Received: 7 December 2010
Accepted: 27 June 2011
Published: 27 June 2011
Toll-like receptors (TLRs) are likely to play crucial roles in the pathogenesis of rheumatoid arthritis (RA). The aim of this study was to determine the key TLRs in synovium and explore their roles in the activation of fibroblast-like synoviocytes (FLSs) mediated by T cells in arthritis.
Pristane-induced arthritis (PIA) was established by subcutaneous injection with pristane at the base of the rat's tail. TLR expression in synovium from PIA rats was detected at different time points by performing real-time PCR. Polyinosinic:polycytidylic acid (poly(I:C)) was intra-articularly administrated to PIA rats, and arthritis was monitored macroscopically and microscopically. Synovial TLR3 was detected by immunohistochemical staining. Rat FLSs were stimulated with pristane-primed T cells or pristane-primed, T-cell conditioned medium. The intervention of TLR3 in FLSs was achieved by specific short-hairpin RNA (shRNA) or an antibody. The migration ability of FLSs was measured by using the scratch test, and gene expression was detected by using real-time PCR. FLSs from RA patients were stimulated with various cytokines and TLR ligands, and TLR3 expression was detected by performing real-time PCR. In addition, with different concentrations of poly(I:C) stimulation, TLR3 expression of FLSs from RA patients and patients with osteoarthritis (OA) was compared.
Synovium TLR3 displayed early and persistent overexpression in PIA rats. TLR3 was expressed in FLSs, and local treatment with poly(I:C) synergistically aggravated the arthritis. Rat FLSs co-cultured with pristane-primed T cells showed strengthened migration ability and significant upregulation of TLR3, IFN-β, IL-6 and matrix metalloproteinase 3 (MMP3) expression, which could also be induced by pristane-primed, T-cell conditioned medium. The upregulation of cytokines and MMPs was blocked by shRNA or TLR3 antibodies. In RA FLSs with cytokine or TLR ligand stimulation, TLR3 expression exhibited remarkable upregulation. Furthermore, RA FLSs showed higher reactivity than OA FLSs to poly(I:C).
TLR3 in the synovium of PIA rats was overexpressed, and activation of the TLR3 signaling pathway could aggravate this arthritis. The induction of TLR3 in FLSs resulted from T cell-derived inflammatory stimulation and could further mediate FLS activation in arthritis. We conclude that TLR3 upregulation of FLSs activated by T cells results in articular inflammation.
Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by synovial inflammation, cartilage and bone erosion and pannus formation [1, 2]. Synovitis manifesting synoviocyte proliferation and activation has been considered the main cause of the secretion of proinflammatory cytokines and chemokines, the recruitment of inflammatory cells and the production of matrix metalloproteinases (MMPs) [3, 4]. Accumulating evidence highlights a role of Toll-like receptors (TLRs) in mediating the synovial inflammatory response [5, 6].
TLRs belong to the pattern recognition receptor family and connect innate and adaptive immunoresponses. Stimulation of TLRs with their ligands activates NF-κB, mitogen-activated protein kinase and IFN regulatory factor pathways . A direct consequence of antigen-presenting cell activation by TLRs is to enhance the secretion of cytokines, as well as the upregulation of major histocompatibility complex (MHC) and costimulatory molecule expression, which facilitate the activation of adaptive immune responses .
It has been demonstrated that many TLRs are constitutively expressed in immune cells and synoviocytes. Previous studies have shown that TLR2, TLR3, TLR4 and TLR7 are overexpressed in the synovial tissue of RA patients [9–11] and that TLR2 and TLR4 expression in peripheral blood cells and macrophages from RA patients is also upregulated . Interestingly, TLR ligands, such as peptidoglycan (PGN), CpG DNA, heat shock proteins and RNA from both infectious organisms and endogenous necrotic cells, have been identified in the joints of RA patients [13–15]. Such exogenous and endogenous TLR ligands have been shown to induce arthritis in mice upon intra-articular injection [16, 17]. The synoviocytes activated by TLR ligands could produce proinflammatory cytokines and chemokines, such as TNF-α, IL-15, IFN-β, granulocyte chemotactic protein 2, RANTES (regulated on activation normal T-cell expressed and secreted) and monocyte chemotactic protein 2, which might contribute to synovitis maintenance and inflammatory cell infiltration [15, 18–20]. Activated synoviocytes could also secrete MMPs, RANKL (receptor activator of NF-κB ligand) and vascular endothelial growth factor, which are involved in the cartilage degradation, joint destruction and angiogenesis in joints [10, 21, 22]. Thus, TLRs may play a vital role in mediating the synovial inflammation in both RA and experimental arthritis . However, the relative role of the different TLRs in mediating and regulating arthritis is still unclear.
In a previous study, we found that TLR3 is the earliest and most prominently upregulated TLR in splenic macrophages by screening the TLR expression profile in pristane-induced arthritis (PIA), a MHC class II-restricted and T-cell-dependent arthritis rat model, and that downregulation of TLR3 expression modulates the severity of arthritis . These findings regarding TLR3 provide an explanation for the initiation of the inflammatory response in immune organs, but the roles of TLRs in local inflammation of joints are still unclear. We hypothesize that a TLR may be induced by arthritogenic T cells and then mediates the activation of synoviocytes in local inflammatory responses. The aim of the present study was to answer the question which TLR is probably the key TLR in synovium in arthritis, whether triggering of the key TLR directly affects arthritis severity and how the key TLR in synoviocytes is induced to mediate the local inflammatory response.
Materials and methods
Dark Agouti (DA rats were bred in a specific pathogen-free animal house at the Department of Genetics and Molecular Biology, Xi'an Jiaotong University School of Medicine, Shaanxi, People's Republic of China. Age- and sex-matched rats were used in all experiments, and each group contained 8 to 10 rats 8 to 12 weeks old. The experiments were approved by the Institutional Animal Ethics Committee of the university.
Arthritis induction and evaluation
Arthritis was induced by a single subcutaneous injection of 300 μL of pristane (ACROS Organics, Morris Plains, NJ, USA) at the base of the rat's tail. Arthritis development and severity were monitored by the change in the perimeter of the ankle and midpaw and assessed using a macroscopic scoring system as described previously .
For pathological examination, ankle joints of rats were sectioned and stained with H & E. The pathological severity of synovitis was estimated on the basis of four items: (1) the thickness of the synovium lining layer, (2) pannus, (3) synovium inflammatory cells and (4) angiogenesis. Each pathological item was scored on a scale ranging from 0 (normal) to 3 (most severe). Finally, synovitis was estimated by adding the scores on items one through four, and the maximum histopathological score was 12 for each ankle.
Primer information for real-time PCR
Gene accession number
Annealing temperature, °C
β- ACTIN (human)
The paraffin-embedded ankle joints from each rat were sectioned, and endogenous peroxidase was blocked with 0.3% H2O2 for 10 minutes. Each section was treated with 10 M urea and Antigen Repair solution I (Wuhan Boster Biological Technology, Ltd., Wuhan, China) for antigen repair and blocked with 1% bovine serum albumin. Then the slide was incubated with an anti-TLR3 polyclonal antibody (1:100 dilution; Santa Cruz Biotechnology, Santa Cruz, CA, USA) or control (rabbit immunoglobulin G (IgG)) overnight at 4°C, and the SABC Kit (Wuhan Boster Biological Technology, Ltd., Wuhan, China) was used for signal amplification and visualization according to the manufacturer's instructions. All sections were stained with 3,3'-diaminobenzidine and counterstained with hematoxylin.
Administration of TLR ligands to PIA rats
Sixteen DA rats were used for polyinosinic:polycytidylic acid (poly(I:C)) administration experiments. Briefly, half of the rats were injected subcutaneously with 150 μL of pristane, and the other half were injected with normal saline (NS). At day 5 after pristane injection, 50 μg of poly(I:C) (Amersham Biosciences, Piscataway, NJ, USA) in 10 μL of NS were injected intra-articularly into one side ankle cavity of each rat in both groups, and the same volume of NS injected into the contralateral ankle served as a control . The paws were divided into four groups: a pristane-poly(I:C) group (injection with systematic pristane and local poly(I:C)), a pristane-NS group, a NS-poly(I:C) group and a NS/NS group. Arthritis symptoms were evaluated in a blinded fashion every two to four days by using a macroscopic scoring system, and the perimeter changes in the ankles and midpaws were evaluated until D26. After the rats were killed, the synovium was collected for RNA quantitation. In another experiment, the joints were collected at D7 and D14 after pristane injection for pathological examination.
Rat fibroblast-like synoviocyte and T-cell co-culture
Synovial fibroblasts from DA rats were isolated by collagenase digestion, cultured as described previously and used after passage 4 . After four passages, the cells were morphologically homogeneous and exhibited the appearance of synovial fibroblasts, with a typical bipolar configuration visualized by inverse microscopy. The purity of the cells was detected by flow cytometric staining using antivimentin antibody , and the proportion of intracellular vimentin-positive cells was more than 95%.
Spleens from PIA rats and control rats were homogenized as a single-cell suspension, and red blood cells were lysed with 0.84% NH4Cl. Next, pristane-primed T cells and control T cells were isolated from the spleen single-cell suspensions by using the Nylon Fiber Column T (Wako Pure Chemical Industries Ltd., Osaka, Japan) as described previously . All T cells were cultured in RPMI 1640 medium supplemented with 10% fetal bovine serum (FBS) and 3 μg/mL Concanavalin A (Con A; Sigma, St. Louis, MO, USA) for 72 hours before use.
Fibroblast-like synoviocytes (FLSs) were seeded into six-well plates at a density of 1 × 105 cells/well in DMEM supplemented with 10% FBS for 24 hours, then the medium was replaced and pristane-primed and control T cells activated by Con A were added at FLS:T cell ratios 5:1, 1:1, 1:5 and 1:10. After 24 hours of co-culturing, suspended T cells were washed with PBS and the remaining FLSs were used to isolate RNA for gene expression study.
Rat FLS migration ability assay
Rat FLSs were plated for 24 hours as described above, and a 100-μL tip (Axygen Scientific, Inc., Union City, CA, USA) was used to draw a streak uniformly in each well, and the initial width (0 hour) of the streak was measured using Image-Pro Plus software (Media Cybernetics, Silver Spring, USA) and an inverted microscope (Olympus Co., Tokyo, Japan). Next, FLSs were co-cultured with pristane-primed and control T cells as ratios of 1:1 and 1:5, respectively, and the widths of the streaks were measured after 24 and 48 hours of co-culturing. FLS migration ability was calculated using the formula[(the initial width)-(the width after 24 or 48 hours of co-culturing)]/(the initial width)*100%.
Rat FLS treatment with T-cell conditioned medium
Pristane-primed T cells and control T cells were isolated and cultured with Con A activation for 72 hours as described above, then the supernatant of the culture medium was collected and filtered through a 0.45-μm filter (Millipore, Eschborn, Germany). Rat FLSs were plated and incubated with pristane-primed T-cell or control T-cell conditioned medium for 24 hours, and TLR3, cytokine and MMP expression of FLSs was detected by performing real-time PCR.
Intervention of TLR3 in rat FLSs
The pGC Silencer™ U6-Neo-GFP-RNAi plasmid (Genechem, Shanghai, China) containing the target sequence of the rat tlr3 gene (ACC TCG ACC TCA CAG AGA A as TLR3 shRNA) was used for TLR3 interference, and the sequence of the negative control shRNA (NC-shRNA) was TTC TCC GAA CGT GTC ACG T . Briefly, FLSs were seeded into six-well plates at a density of 1 × 105 cells/well and transfected with the plasmids plus Lipofectamine™2000 reagent (Invitrogen, Carlsbad, CA, USA). TLR3 expression in FLSs was detected after 24-hour transfection for the knockdown efficiency assay. In T-cell co-culture experiments, TLR3-knocked-down FLSs were co-cultured with pristane-primed T cells at a ratio of 1:10, and the cytokine and MMP expression of FLSs was detected by performing real-time PCR after 24 hours. In a T-cell conditioned medium stimulation experiment, TLR3-knocked-down FLSs were incubated with pristane-primed T-cell conditioned medium for 24 hours, and the gene expression of FLSs was detected by real-time PCR.
In a TLR3 blockade assay, FLSs were seeded into six-well plates at a density of 1 × 105 cells/well. FLSs were treated with anti-TLR3 or isotype control antibodies at the concentration of 20 μg/mL for 90 minutes before co-culture with pristane-primed T cells at the ratio of 1:10 as described previously . After 24-hour incubation, the gene expression of FLSs was detected by real-time PCR.
Human synovial tissue preparation and FLS stimulation
Human synovial tissues were obtained from three RA patients and three osteoarthritis (OA) patients undergoing knee joint replacement surgery. All RA patients fulfilled the American College of Rheumatology criteria for the classification of RA . OA was diagnosed according to the patients' clinical features. The Human Ethics Committee of Xi'an Jiaotong University approved this study, and the written, informed consent of all patients was obtained.
The FLSs from RA or OA patients were isolated as described previously . FLSs were seeded into six-well plates at a density of 1 × 105 cells/well. After 24 hours, RA FLSs were stimulated with 10 ng/mL TNF-α, 1 ng/mL IL-1β, 1 ng/mL IFN-α, 1 ng/mL IFN-β, 10 μg/mL PGN, 10 μg/mL poly(I:C) and 10 ng/mL lipopolysaccharide (LPS), respectively. RA and OA FLSs were stimulated with 1, 10 and 100 μg/mL of poly(I:C). After 24-hour stimulation, cells were lysed with TRIzol reagent and TLR3 expression was detected by real-time PCR.
Quantitative data are expressed as means ± SEM. Statistical analysis was performed by using Student's t-test, the Mann-Whitney U test or two-way analysis of variance. Correlation analysis was performed by using Spearman's σ test. P < 0.05 was regarded as statistically significant.
TLR3 expression of synovium exhibited a remarkable increase in the PIA rat model
Next, we localized TLR3 protein expression in the ankles of PIA rats by immunohistochemical staining, and strong TLR3 staining was observed at synoviocytes, especially at hyperplastic FLSs (Figure 1C). Obviously, FLSs from PIA joints expressed TLR3 predominantly at sites of attachment and invasion into cartilage and bone (Figure 1C).
Poly(I:C) mediated by TLR3 aggravated the severity of PIA
The ankle sections obtained at D7 and D14 were stained with H & E. The poly(I:C) injection groups, comprising the NS/poly(I:C) group and the pristane/poly(I:C) group, showed pathologic changes with abundant inflammatory cell infiltrates and synovium hyperplasia at D7. The pathologic changes in the NS/poly(I:C) group recovered at D14, but those in the pristane/NS group and the pristane/poly(I:C) group became aggravated with obvious bone and cartilage destruction, especially in the pristane/poly(I:C) group (Figure 2B). The pathological scores with regard to synovitis showed a significant difference between the NS/poly(I:C) group, the pristane/poly(I:C) group and the NS/NS group at D7 (Figure 2C). Not surprisingly, the pristane/poly(I:C) group and the pristane/NS group had higher synovitis scores at D14 compared with the NS/NS group and the NS/poly(I:C) group. The synovitis of the pristane/poly(I:C) group was more severe than that of the pristane/NS control group (Figure 2C).
Both the pristane/poly(I:C) group and the pristane/NS group had increased TLR3 mRNA expression in synovium at D26 compared with the NS/NS group (Figure 2D). In contrast, TLR3 expression did not differ between the NS/poly(I:C) group and the NS/NS group (Figure 2D). TLR3 mRNA expression correlated with the clinical indexes: the changes in ankle and midpaw perimeters (Figure 2D). On the basis of the ligand stimulation experiment, we concluded that overexpression of TLR3 in FLSs was involved in mediating arthritis development. However, the mechanism of the induction of TLR3 expression in FLSs was still unknown, so a co-culture of FLSs and splenic T cells was performed to investigate whether TLR3 might be induced by infiltrated T cells and then involved in synoviocyte activation.
Rat FLSs were activated by pristane-primed T cells with increased TLR3 expression
After being exposed to pristane-primed T cells for 24 and 48 hours, FLSs also showed enhanced migration ability when the co-culture ratios of FLSs and T cells were 1:1 and 1:5 (Figure 3B). Coincidentally, IFN-β, IL-6 and MMP3 expression of FLSs, which were stimulated with pristane-primed T cells for 24 hours, showed significantly high levels compared with those stimulated with control T cells, whereas MMP13 expression showed a trend toward upregulation (Figure 3C). Obviously, TLR3 expression in FLSs was induced by pristane-primed T-cell stimulation, and the FLSs were activated with more cytokine and MMP secretion. Whether synoviocyte activation was mediated by the TLR3 signaling pathway needed to be confirmed by conducting a TLR3 intervention experiment.
Intervention of TLR3 blocked the activation of FLSs stimulated by pristane-primed T cells
Besides downregulation of TLR3 by RNAi, TLR3 antibody was used to block the TLR3 signaling pathway in rat FLSs. With TLR3 antibody or isotype IgG preincubation, rat FLSs were co-cultured with pristane-primed T cells at the ratio of 1:10 for 24 hours. All expression of IFN-β, IL-6, MMP3 and MMP13 was significantly reduced in the TLR3 antibody treatment group (Figure 4C).
Soluble inflammatory factors from T cells activated FLSs via TLR3 in rats
Next, we used TLR3-specific RNAi to interfere with TLR3 expression in FLSs. After 24-hour transfection, TLR3 expression showed significant downregulation in FLSs transfected with TLR3-shRNA plasmid (Figure 5C). Then FLSs transfected with TLR3-shRNA and NC-shRNA plasmids were incubated with pristane-primed T-cell conditioned medium for 24 hours. Compared with the NC-shRNA group, the results showed significant downregulation of IFN-β and MMP-13 and, to a lesser extent, MMP-3 in the TLR3-shRNA group (Figure 5D). However, IL-6 was not blocked by the TLR3 RNAi, suggesting that other regulation mechanisms might be present. Overall, the data confirmed that soluble inflammatory factors from T cells could be the main source driving the activation of FLSs via TLR3 in rats.
TLR3 expression in FLSs from humans was induced by soluble factor stimulation
Many TLRs in previous studies of RA have been reported to play a vital role in the pathogenesis of arthritis. However, which TLR is key to mediating the initiation and maintenance of joint inflammation is still unclear, owing to the limited number of patient samples. Accordingly, a single subcutaneous injection of pristane in DA rats led to chronic relapsing arthritis similar to RA in humans. We comparatively analyzed the expression of TLR1 through TLR9 in synovium during the whole course of arthritis initiation and development to investigate the roles of TLRs systematically and dynamically in a PIA model. Nearly all TLR expression showed a transient induction at the early stage (D6), at which point arthritis had not yet occurred. This finding is probably due to the general stress reaction stimulated by pristane, since we have observed that there is a systemic inflammatory response in spleen and lymph nodes with the activation of TLRs and the secretion of proinflammatory cytokines . Therefore, more attention to the disease onset and development phases should be a priority. Surprisingly, we have demonstrated in the present study that a compelling TLR is TLR3, which has early and stable overexpression in synovium exclusively at initiation and development stages of arthritis. Coincidentally, in the PIA rat model, IFN-β, a TLR3-related cytokine, and IL-6 showed significant increases at D26. TLR3 has been reported to be expressed mainly on dendritic cells and fibroblasts, as well as on murine macrophages . In the synovium of RA patients, it has been found that most of the synoviocytes that expressed TLR3 are synovial fibroblasts, except macrophages [10, 15]. Consistent with previous observations in humans, TLR3 protein expression was detected by immunohistochemical staining in FLSs of PIA rats, suggesting that FLSs constitute a major cellular source of TLR3 production in inflamed synovial tissue. In other words, the hyperplasia and activation of FLSs might be mediated by TLR3 signaling. One possibility is that upregulated TLR3 could recognize the RNA released from necrotic synovial fluid cells and then activate RA synovial fibroblasts to promote cytokine secretion and expedite osteoclastogenesis [15, 32].
According to the above findings, we suggest that TLR3 in FLSs may play an important role in the local inflammation of PIA. In a previous study, intra-articular treatment with poly(I:C) was found to cause a rapid and strong synovitis in rats , which suggests the involvement of TLR3 signaling in inflammation mediation. To confirm that overexpression of TLR3 in FLSs is functional in joint inflammation induced by pristane, we administrated poly(I:C) locally to PIA rats and observed the synergistic effect. The results showed that PIA rats intra-articularly treated with poly(I:C) compared with rats treated with poly(I:C) alone exhibited more persistent inflammation and joint destruction, which might be due to the upregulation of TLR3 expression in PIA. Meanwhile, comparing the PIA group and the PIA/poly(I:C) group, we found that treatment with poly(I:C) could exacerbate arthritis, especially at the initial stage of arthritis, according to both the clinical and pathological results. Obviously, the above results confirm that there is a strong synergistic effect between pristane and poly(I:C). TLR3 expression was upregulated in both pristane treatment groups, especially in the pristane/poly(I:C) group, and significantly correlated with arthritis severity, suggesting that the activation of TLR3 on fibroblasts triggered by poly(I:C) causes more severe arthritis. These results validate the importance of TLR3 in PIA in vivo. However, the cause of the upregulation of TLR3 expression and the activation of FLSs in arthritis is not known yet.
Accumulating evidence favors the involvement of an adaptive autoimmune process in the etiopathogenesis of RA and experimental arthritis [33, 34]. Recently, several models of spontaneous arthritis due to perturbations in the TCR signaling pathway have been identified, and the effector mechanisms in the model are T cell-mediated . Moreover, the vast majority of lymphocytes infiltrating RA synovium are CD4+ αβ T cells [36, 37]. PIA is also a T-cell-dependent disease which can be transferred with CD4+ αβ T cells . T cells isolated from the spleens of PIA rats transfer severe arthritis, showing that the critical arthritogenic change induced by pristane is present in the spleen. Meanwhile, there is a selective accumulation of activated CD4+ T cells in PIA synovial membrane. Administration of anti-CD4 antibody, but not anti-CD8 antibody, can ameliorate PIA (W Zhu, L Meng, J Tuncel, S Carlsen, S Lu and R Holmdahl. unpublished data). These data suggest that the splenic, pristane-primed, arthritogenic T cells, which specifically infiltrate into joints, might be the inflammatory trigger for FLS activation, joint destruction and arthritis chronicity. Thus, we co-cultured the splenic T cells with rat FLSs to investigate the intercellular interaction in synovial inflammation. It was a surprising finding that pristane-primed T cells significantly elevated TLR3 expression in FLSs and that FLSs also exhibited an enhanced migration ability and increased cytokine and MMP secretion. In other words, the activated T cells in the organs of the immune system led to the induction of FLSs in arthritic joints. Meanwhile, we found that other TLR expression was regulated erratically. With the exception of TLR3, TLRs were not induced significantly under the co-culture ratio of 1:5, suggesting that TLR3 might be preferentially induced with pristane-primed T cell-specific stimulation. With the maximum co-culture ratio (1:10), nearly all TLR (but not TLR1) expression was increased, which was probably due to the secondary inflammatory response. Taken together with the comprehensive analysis, we considered that TLR3 should be a more important and specific TLR in FLS induction and thus we gave priority attention to TLR3 in our following work, although we still could not rule out other TLR roles in joint inflammation, which need to be confirmed by further studies.
Intervention of both TLR3 expression and the TLR3 signaling pathway in FLSs blocked the upregulation of cytokines and MMPs stimulated by pristane-primed T cells, suggesting that the TLR3 signaling pathway induced by T cells actually caused the FLS activation. However, the questions how T cells upregulate TLR3 expression in FLSs, and whether TLR3 induction is due to cell-cell interaction or to T cell-derived soluble factor stimulation, were still equivocal. Thus, we utilized the T-cell conditioned medium instead of T cells to be incubated with the FLSs and found that FLSs with pristane-primed T-cell conditioned medium showed strong induction of TLR3 expression and increased production of cytokines and MMPs. The increased secretion of IFN-β and MMPs, but not IL-6, in FLSs was blocked by TLR3-specific RNAi. The above in vitro data suggested that the stimulation of soluble factors derived from T cells might be the main cause of TLR3 upregulation, which subsequently activated FLSs, although we still could not rule out the role of cell contact. IL-6 upregulation, which could be induced by a variety of stimuli, seemed not to depend on TLR3, suggesting that IL-6 might be regulated by other mechanisms.
The pristane-primed arthritogenic T cells which are used to transfer arthritis could secrete IFN-γ and TNF-α with Con A stimulation in vitro, and pretreatment of recipient rats with either anti-IFN-γ or a recombinant TNF-α receptor before transfer, ameliorated arthritis development . Other cytokines are also considered to be involved in arthritis, however, and biological medicines targeting them (such as IL-1, IL-6 and IL-17) were developed in different clinical trials . Thus, the question of which key cytokines participate in mediating local inflammation in joints is still interesting. In our rat experiments, we comprehensively used inflammatory factors to stimulate FLSs from RA patients to confirm the universality of TLR3 induction in the human system. All chosen factors, including proinflammatory cytokines and ligands of TLRs, which had been reported to be involved in RA successfully induced the upregulation of TLR3 expression. With poly(I:C) treatment, we observed an enhanced increase in TLR3 expression in RA FLSs compared with OA FLSs, suggesting that TLR3 signaling in RA FLSs has a lower activation threshold. These findings validate that in RA, not only in PIA, TLR3 signaling mediates the FLS activation induced by inflammatory stimulation.
In summary, TLR3 in the synovium of PIA rats displayed early and persistent overexpression at the initiation and development stages of arthritis. TLR3 was localized in FLSs, and activation of the TLR3 signaling pathway in vivo could aggravate arthritis. FLSs were activated and made functional by the T cell-derived inflammatory mediator via TLR3 signaling in arthritis. Thus, TLR3 was confirmed to be an important mediator to bridge T cells and FLSs in arthritis. These data provide a very useful experimental example to increase understanding of the initiation and development of synovial inflammation systemically and dynamically, and also provide an interesting target for RA treatment.
Dulbecco's modified Eagle's medium
- H & E:
hematoxylin and eosin
nuclear factor κB
polymerase chain reaction
C): polyinosinic:polycytidylic acid
tumor necrosis factor.
We express gratitude to Fujun Zhang, Yan Han and Qilan Ning for their expertise and assistance with the experiments. This work was supported by grants from the National Natural Science Foundation of China (30801027 and 30630058), the Fundamental Research Funds for the Central Universities of China, the Swedish Research Council, the Swedish Foundation for Strategic Research and the EU project Masterswitch HEALTH-F2-2008-223404.
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