- Research article
- Open Access
Toll-like receptor 3 upregulation in macrophages participates in the initiation and maintenance of pristane-induced arthritis in rats
Arthritis Research & Therapy volume 12, Article number: R103 (2010)
Toll-like receptors (TLRs) are involved in both innate and adaptive immune responses and are likely to play a complex role in the pathogenesis of human rheumatoid arthritis (RA) and experimental arthritis. The objective of this study was to identify the key TLR in pristane-induced arthritis (PIA), a rat model for RA, and to clarify its roles in the initiation and maintenance of arthritis.
Arthritis in DA rats was induced by pristane and the severity was evaluated by macroscopic and microscopic score systems. Spleen TLR and cytokine expression was detected at different time points by real-time polymerase chain reaction (PCR) and flow cytometry. Polyinosine-polycytidylic acid (polyI:C, a ligand of TLR3) or TLR3 specific short-hairpin RNA plasmid for RNA interference was administrated to PIA rats in vivo. Serum nitrogen oxide concentration was determined by Griess method, and tumor necrosis factor alpha (TNF-α) was determined by L929 biotest. In splenic macrophages, TLR3 expression was measured by flow cytometry. A rat macrophage cell line (NR8383) was stimulated by pristane, and anti-TLR3 antibody were used to block TLR3 pathway. TLR3 and cytokine expression in NR8383 were detected by real-time PCR.
By screening the TLR expression profile in spleen of DA rats after pristane injection, we found that TLR3 was the most early and prominently upregulated TLR. Both TLR3 mRNA and protein expression of spleen were upregulated at 6 and 26 days after pristane injection. Furthermore, administration of polyI:C exacerbated, whereas RNA interference targeting TLR3 ameliorated, the arthritis. Particularly, TLR3 expression was induced in splenic macrophages of PIA rats, and also in the NR8383 cell line after pristane stimulation in a dose- and time- dependent manner. Upregulation of interferon beta (IFN-β) and TNF-α by pristane stimulation was blocked by anti-TLR3 antibody in NR8383.
TLR3 plays a pivotal role in the initiation and development of PIA which may dependent on macrophage. These findings are useful to understand the pathogenesis of RA and may provide an intriguing therapeutic opportunity for RA.
Rheumatoid arthritis (RA) is an autoimmune chronic inflammatory syndrome affecting 0.5 to 1% of the world population, and is characterized by cellular proliferation in the synovial lining and cartilage and bone destruction of diarthrodial joints . Genetic and serologic evidence in both RA and experimental arthritis favors the involvement of both innate and adaptive autoimmune processes [2, 3]. Toll-like receptors (TLRs) are pattern recognition receptors, which form a bridge between innate and adaptive immune systems, and have been considered to be an important factor in the development of RA .
TLRs are involved in activation of antigen-presenting cells (APCs) by influencing the uptake and processing of various exogenous and endogenous antigens . Activation of TLRs in APCs not only leads to the upregulation of the costimulatory molecule expression and cytokine secretion [6, 7], but also promotes the T cell polarization [8, 9]. In addition, TLRs could orchestrate the function of regulatory T cells [10, 11].
TLRs are likely to play a complex role in RA, and certain TLRs exhibit a high expression, such as TLR2, 3, 4, 7 in synovium [12–15], TLR3 in fibroblast-like synoviocytes (FLS) , TLR2, 4 in CD14+ macrophages and peripheral blood cells from RA . Both exogenous and endogenous TLR ligands have been detected in synovia, synovial fluids and sera of RA patients [14, 17, 18]. Importantly, these ligands are capable of stimulating FLS and/or immunocytes via triggering TLRs to produce proinflammatory cytokines [12, 19–24], and may also activate the autoreactive T and B cells [25–27]. In particular, injection of TLR2 and TLR9 ligands, peptidoglycan (PGN) and CpG DNA, into articular cavities induces arthritis in mice [28, 29].
Based on the above-mentioned reasons, it seems that TLRs play essential roles in the pathogenesis of RA. However, most studies on RA are descriptive and focus on TLR2 and 4 in synovium. Thus, a systemic study about TLR roles in the initiation of immune response of RA will provide new insight for elucidating the pathogenesis of RA. The TLR genes are highly conserved and using animal models should be reasonable to address the issue of TLR roles in RA development.
Various animal models represent different or partly different disease processes of RA, and a few studies have concerned TLR roles in the pathogenesis of arthritis. TLR2 and 4 were reported to be involved in the chronicity and erosive destruction of streptococcal cell wall induced arthritis and spontaneous arthritis in IL-1 receptor antagonist-knockout mice [8, 30, 31]. TLR4 takes part in the initiation and progression of both autoantibody/lipopolysaccharide (LPS)-triggered arthritis and serum transferred arthritis [32, 33]. It has also been suggested that cathepsin K could ameliorate mycobacteria induced arthritis in rats through suppression of TLR9 signaling in dendritic cells (DCs) . Of particular interest is the pristane-induced arthritis (PIA) model as it is induced with a single subcutaneous injection with a well-defined compound lacking antigenic properties. The induced disease is joint specific and fulfills the clinical criteria of RA [35, 36]. Importantly, the arthritogenic adjuvant stimuli may mimic such a trigger in humans represented by an infectious agent or a non-specific inflammatory response. It is known that pristane induces a strong innate immunity through the triggering of IL-6 production , suggesting that TLRs may participate in and mediate the immune response. Altogether, the mechanism of TLRs involved in experimental arthritis is not understood completely.
In the present study, we tried to find the key TLR in arthritis development by screening the TLR1-9 expression profile in spleen from PIA rats. The results indicated TLR3 showed a unique expression pattern compared with other TLRs in spleen of PIA rats. And in PIA rats treated with polyinosine-polycytidylic acid (polyI:C) or RNA interference (RNAi) of TLR3, arthritis manifestations could be modified. Furthermore, TLR3 may exert its influence in a macrophage-dependent manner. These data illustrated the crucial role of TLR3 in the initiation and development of PIA.
Materials and methods
DA rats were bred in a specific pathogen-free animal house. Each group contained 8 to 10 rats at the age of 8 to 12 weeks. The experiments were approved by the Institutional Animal Ethics Committee of the University (permission No. 2006-21).
Induction and evaluation of arthritis
Arthritis was induced by a single subcutaneous injection with 300 μl of pristane (ACROS Organics, Morris Plains, NJ, USA) at the base of the rat's tail. Arthritis development and severity were monitored every two to four days by the perimeters of ankle and mid-paw, and a macroscopic scoring system as described .
Histopathological examination of joints
Left ankle joints of rats were sectioned and stained with hematoxylin and eosin. Pathological severities were estimated by extent of 10 items: a. thickness of synovium lining layer; b. pannus; c. synovium inflammatory cells; d. angiogenesis; e. cartilage erosion; f. bone erosion; g. joint ankylosis; h. change of overall articular structure; i. new bone formation; and j. new cartilage formation. Each pathological item was scored on a scale consisting of score 0 (normal) to 3 (most severe). The maximum histopathological scores of arthritis are 30 for each ankle. Synovitis was estimated by addition of item a. to d. scores; joint destruction by e. to h. scores; joint healing by i. and j. scores.
Total RNA was isolated with TRIzol® Reagent (Invitrogen, Carlsbad, CA, USA), and cDNA was synthesized by First Strand cDNA Synthesis Kit (Fermentas, Burlington, ON, Canada). Real-time quantitative PCR was performed by iQ5 (BIO-RAD, Hercules, CA, USA) with SYBR® Premix Ex Taq™ II (TaKaRa, Ohtsu, Shiga, Japan) for TLR and cytokine mRNA quantitation. And gene expression was normalized by β-actin. The information on primers, products and annealing temperatures were depicted in Table 1.
Fluorescence-activated cell sorting (FACS) analysis of TLR expression in splenocytes
Three tubes containing 106 splenocytes for cell surface TLR detection were incubated with TLR2, TLR3 and TLR4 antibodies (Santa Cruz Biotechnology, Santa Cruz, CA, USA) respectively. In the other tube for intracellular TLR3, the cells were fixed and perforated before TLR3 antibody incubation. For detection of macrophage TLR3, two tubes containing 106 splenocytes were incubated with HIS36-PE (anti-rat macrophage, eBioscience, San Diego, CA, USA) firstly. And for cell surface TLR3 detection, the cells were incubated with TLR3 antibody at the same time. For intracellular TLR3 detection, the cells in the other tube after His36-PE staining, were fixed and perforated before TLR3 antibody incubation. The cells from both tubes were incubated with goat anti-rabbit IgG-biotin followed by streptavidin-cychrome. Cells were analyzed by using a FACScanto (Becton Dickinson, Franklin Lakes, NJ, USA), and datum analysis was performed using FlowJo software (Tree Star, Ashland, OR, USA).
Administration of TLR ligands to PIA rats
Thirty-six rats were randomly divided into four groups. The control group was injected subcutaneously with 300 μl phosphate buffered saline (PBS) only. Other groups were injected subcutaneously with 300 μl pristane, then administered subcutaneously with 150 μl saline containing 100 μg polyI:C (Amersham Biosciences, Piscataway, NJ, USA) in the polyI:C group, 50 μg LPS (Sigma-Aldrich, St. Louis, MO, USA) in the LPS group, and none in the saline group, respectively, at two days after pristane injection [38, 39].
Cell transfection and treament with TLR3 RNAi in vivo
The target sequences of TLR3 gene are GAA TCA CAT CTC GAA GAT A, called as shRNA1-TLR3; CTC TCA ATT TAA CGA AGA A, as shRNA2-TLR3; ACC TCG ACC TCA CAG AGA A, as shRNA3-TLR3; and CCT GAC AGA GCT CCA TCT A as shRNA4-TLR3. The sequence of negative control shRNA is TTC TCC GAA CGT GTC ACG T. These different short-hairpin RNA (shRNA) sequences were inserted into pGCsilencer™ U6/Neo/GFP/RNAi plasmid (Genechem, Shanghai, China). The plasmids were extracted with E.Z.N.A.™ Endo-free Plasmid Maxi Kit (Omega Bio-tek, Doraville, GA, USA), and NR8383 cells were transfected with Lipofectamin™ 2000 (Invitrogen). TLR3 expression of cells was detected by RT-PCR after 24 hours and by FACS after 48 hours. DA rats randomly divided into three groups were injected subcutaneously with 300 μl pristane. At one day before pristane injection, and 5, 11 and 17 days after pristane injection, 1 ml of saline was injected peritoneally into the rats in the saline group; 50 μg shRNA3-TLR3 in 1 ml of saline in the shRNA-TLR3 group; and 50 μg negative control shRNA in 1 ml of saline in the shRNA-NC group [40, 41]. At 20 days after pristane injection (d20), GFP mRNA expression was detected by RT-PCR to monitor the plasmid presence in spleen (Primer information was depicted in Table 1). And TLR3 mRNA expression in the spleen was detected by real-time quantitative PCR for determination of the RNAi effectiveness.
Measurement of NO concentration
Serum protein was removed, and NO3- was reduced to NO2- by using cadmium filings. Then NO2- was measured by a microplate assay method based on the Griess reaction.
Measurement of TNF-α concentration
The mouse fibroblast cell line, L929, was cultured in RPMI 1640 (Hyclone, Logan, UT, USA) containing 10% FCS. Ten thousand cells in 100 μl were incubated for 24 hours. Then sera containing 1 mg/ml actinomycin D were added to replace the original medium. After an 18-hour incubation, cell viability was evaluated by the methyl thiazolyl tetrazolium method. Rat recombinant TNF-α (Bender MedSystems Inc., Burlingame, CA, USA) was used as the standard.
Stimulation of macrophages with pristane
The rat macrophage cell line, NR8383, was cultured in F-12 K medium (Sigma-Aldrich) with 20% FBS (Hyclone). Emulsion of pristane was made by repeated aspiration with PBS. Half-million cells per well were put in a six-well plate, then a 50 μl pristane emulsion was added in the culture medium. The theoretical pristane concentration is 0.1, 1, 10, 100 μM, 1 mM and 10 mM, calculated on the basis of original volume of pristane employed. The cells were collected after 8, 24, 48 and 72 hours of stimulation.
TLR3 blockade assay in NR8383
NR8383 were seeded in six-well plates at a density of half-million per well. In the TLR3 Blockade assay, cells were treated with anti-TLR3 or isotype control antibodies at a concentration of 20 μg/ml for 90 minutes before being stimulated with 100 μM pristane or 10 μg/ml polyI:C. The cells were collected after 24 hours' stimulation.
Quantitative data were expressed as means ± SEM. The statistical analysis of differences between experimental groups was performed by Mann-Whitney U test or Student's T test. Correlation analysis was performed by Pearson test. P < 0.05 was considered significant.
TLR3 expression of spleen exhibits a remarkable increase in the PIA rat model
Arthritis-susceptible DA rats were given a single subcutaneous injection of pristane known to induce arthritis within two weeks . The spleens were isolated and analyzed for mRNA expression at different time points. The results showed that only TLR3 mRNA expression was upregulated as early as six days after pristane injection (d6) (Figure 1a). TLR1-4 and TLR8 were significantly expressed at 26 days after pristane injection (d26) (Figure 1a). However, TLR5, 6, 7, 9 did not show a significant change after pristane injection. Another independent experiment was performed with more time points, 2 and 12 (d12) days after pristane injection. TLR3 expression increased dynamically and progressively with the arthritis initiation and development. It was significantly upregulated at d6 and d26, and had a high level at d12 (Figure 1b). IFN-β, known to be triggered by TLR3, was upregulated at d6 and d26 (Figure 1c). Of the proinflammatory cytokines, TNF-α and IL-6 mRNA expression only increased at d6 (Figure 1c). And IFN-γ mRNA expression at d6 and d26 had no difference comparing with control group (d0).
Based on the expression at mRNA level, we determined the protein expression of TLR2, 3 and 4 in the spleens of PIA rats by flow cytometric staining. The results showed that the proportion of cell surface TLR3 positive cells increased significantly at d6 and d26, while that of intracellular TLR3 positive cells and cell surface TLR2 and 4 positive cells increased significantly only at d26 (Figure 1d).
The administration of TLR3 ligand increases arthritis severity
The pristane pre-injected rats were treated with ligands of TLR3 (polyI:C), TLR4 (LPS) and saline, respectively. The clinical score of the polyI:C group showed significant increase compared with the saline group and the LPS group from 15 days after pristane injection, and maximum clinical score of the polyI:C group consistently had a significant difference compared with other groups (Figure 2a). Maximum perimeters of hind paw and ankle also increased in the polyI:C group (Figure 2a). Serum NO concentration increased significantly in all PIA groups, in particular in the polyI:C group (Figure 2b), but there are no differences among all pristine-treated groups. TNF-α concentration in the polyI:C group increased significantly compared with other groups (Figure 2b).
Histopathologically, polyI:C administration aggravated the pathologic changes with abundant inflammatory cell infiltrates and bone destruction (Figure 2c). PolyI:C group showed significant differences with the LPS group and the saline group in the pathological score of synovitis, joint destruction, new bone and cartilage formation (Figure 2d). Meanwhile, the total pathological score of polyI:C group had significantly increased compared with other groups (Figure 2d). All results from the clinical, serological and pathological data indicated that TLR3 ligand administration to the PIA rats could make the disease more severe, and further highlighted the important role of TLR3 in PIA development. Then RNAi of TLR3 in vivo was performed to convince the authors that TLR3 is essential in PIA pathogenesis.
The RNAi of TLR3 significantly ameliorates PIA in rats
NR8383 macrophages were transfected with four different TLR3 shRNA plasmids to determine whether the expression of TLR3 could be downregulated. Results from RT-PCR and flow cytometric staining showed that shRNA3-TLR3 most efficiently downregulated TLR3 mRNA and protein expression (Figure 3a, b). The plasmids, shRNA3-TLR3 (shRNA-TLR3 group) and shRNA-NC (shRNA-NC group, as a negative control), were applied to PIA rats in vivo. The GFP gene in the plasmid treatment groups, except for the saline group, was successfully amplified by RT-PCR (Figure 3c), which showed that plasmids with peritoneal injection in rats could accumulate in the spleen. And TLR3 mRNA expression in the spleen of the shRNA-TLR3 group was significantly lower than that of the shRNA-NC group at d20 (Figure 3d). The clinical score of the shRNA-TLR3 treated rats was lower than that of the shRNA-NC and saline treated rats from 16 days after pristane injection (Figure 3e). The PIA onset day of the shRNA-TLR3 group was later than that of the other two groups (Figure 3e). The shRNA-TLR3 group showed a significantly lower maximum score compared with the other two groups (Figure 3e). The NO concentration in the shRNA-TLR3 group was significantly lower than that of the saline group (Figure 3f). Results indicated that the knockdown of TLR3 expression can ameliorate the disease after pristane injection in rats.
TLR3 expression was induced in macrophages with pristane stimulation
TLR3 expression in splenic macrophages was detected by flow cytometric staining in PIA rats. The mean fluorescence intensity (MFI) of cell surface TLR3 positive cell increased markedly at d6 and the proportion increased significantly at d26, although the intracellular TLR3 expression showed no change after pristane injection, suggesting that the role of TLR3 in the pathogenesis of the disease seems to be associated with the high expression on the macrophage membrane (Figure 4a).
To confirm the role of pristane on TLR3 expression upregulation in macrophages, we stimulated NR8383, a rat macrophage cell line, with pristane. We found that TLR3 mRNA expression was increased in a dose-dependent manner after pristane stimulation, and reached the peak at 1 mM pristane (Figure 4b). In contrast, TLR4 mRNA expression did not show a dose-dependent tendency. TLR3 expression was induced already at 8 hours after pristane stimulation, and was highest at 24 hours (Figure 4c). IFN-β mRNA expression also showed a pattern similar to TLR3, and increased significantly in the group stimulated at 24 and 48 hours (Figure 4d). TNF-α mRNA expression increased significantly at 24 and 48 hours (Figure 4d). However, as NR8383 were pretreated with anti-TLR3 antibody, the upregulation of IFN-β and TNF-α expression stimulated by both pristane and polyI:C was inhibited significantly (Figure 4e). The result indicated that in macrophages pristane certainly orchestrated high TLR3 mRNA expression, which activated the downstream cytokine pathway.
A single subcutaneous injection of pristane in DA rats leads to chronic relapsing arthritis similar to RA in humans. We now show that pristane injection also leads to an upregulated expression of TLRs, in particular TLR3. TLR3 was found to play a critical role in the development of arthritis as an injection of TLR3 ligand enhanced arthritis and downregulation of TLR3 through treatment with RNAi alleviated arthritis. And TLR3 expression was induced with pristane stimulation particularly in macrophages.
PIA is a T cell dependent disease, which can be transferred with αβT cells , and there is no evidence so far arguing for a pathogenic role of B cells. In the human disease it is clear at present that many patients benefit from depletion of B cells through injection of antibodies to CD20. In contrast, in PIA antibodies to citrullinated proteins are not evoked and there is no evidence for pathogenic antibodies mediating the disease, unlike in the collagen-induced arthritis model. However, the immune response in PIA also shows some striking similarities with RA since rheumatoid factors and antibodies to RA33 are produced in both diseases . Importantly, a strong activation of an innate response is apparent in both RA and PIA, although in RA it has been possible to analyze the response only in already established disease. In RA synovial tissues a strong overexpression of TLR3 and 4 has been reported, whereas isolated macrophages show high expression of TLR2 and 4 [13, 16]. But there has been no study on TLRs in the PIA rat model so far.
A subcutaneous injection of mineral oil or phytol, structurally similar to pristane, leads to an accumulation of oil at the injection site but also a rapid spread of small volumes to draining lymph nodes and subsequently spreads systemically, reaching the spleen [44, 45]. Previous studies have shown that T cells isolated from spleens, less than eight days after pristane injection, transfer severe arthritis, showing that the critical arthritogenic change induced by pristane is present in the spleen . Therefore we selected the spleen to study the innate immune reaction after pristane injection.
Screening TLR mRNA expression at different time points after pristane injection, we found that expression of TLR1, 2, 3, 4 and 8 in the spleen is upregulated in the development stage of arthritis (d26), which is consistent with previous studies from arthritis models and RA patients [20, 22, 23, 46]. A compelling TLR is TLR3 as it was highly expressed uniquely in the early phase, and increased progressively with the development of the disease. It has been reported that TLR3 is overexpressed in synovial tissue from both early and longstanding RA [12, 13]. A possible pathogenic role of the upregulated TLR3 could be that it recognizes RNA released from necrotic synovial fluid cells, and then activates RA synovial fibroblast . TLR3 combined with TLR4, TLR7/8 is also involved in the regulation of DC activation and cytokine production in RA patients . It indicates that TLR3 in the spleen may play a vital role in PIA. To examine whether the observed TLR overexpression has functional consequences, downstream cytokines of TLR pathway, such as TNF-α, IL-6, IFN-γ and IFN-β mRNA expression in the spleen were determined. IFN-β expression was found to increase at both d6 and d26, whereas TNF-α and IL-6 expression only increased at d6, and the IFN-γ expression level did not change. These proinflammatory cytokines are known to be regulated by many TLRs via several intracellular pathways but are mainly associated with NF-κB. TLR3 and possibly TLR4 activate interferon regulatory factor 3 which regulates IFN-β expression . By flow cytometric staining we confirmed high TLR3 protein expression in splenocytes. The expression of TLR3 on splenocyte surfaces increased at d6 and d26, reflecting its mRNA expression pattern.
Based on the experimental data from the gene expression profile and TLR2, 3, 4 protein expression during the disease course, we suggest that TLR3 plays an important role in the pathogenesis of PIA. Such a role could be confirmed through in vivo experiments with TLR3 ligands and RNAi. In a previous study, intra-articular treatment with polyI:C to rats caused a rapid and strong synovitis , which suggested the important role of TLR3 signaling in arthritis pathogenesis. And in our research, the systemic treatment with polyI:C synergism with pristane showed that TLR3 ligand could exacerbate arthritis. This dominant role of the TLR3 ligand was also proved by pathology of the PIA rat ankles. The possible mechanism of polyI:C's effect on PIA could be that more TLR3 is activated by polyI:C, which triggers more severe inflammatory reaction in joints. Meanwhile, the results also emphasize the important roles of the ligand in arthritis pathogenesis. But at present, it is still not defined which endogenous ligand of TLR3 participates in PIA. Thus, priority should be given to exploring the probable ligand and investigating its roles in arthritis.
A crucial role of TLR3 in the PIA pathogenesis could also be confirmed by treatment with RNAi in vivo. The shRNA plasmids did not show any immunostimulatory effect in vivo because the shRNA-NC group shows no differences from the saline group in all indexes. The results indicated that the RNAi of TLR3 participated in the initiation of PIA significantly delayed the onset day and decreased arthritis severity. NO concentration of shRNA-TLR3 group was also significantly lower than that of the shRNA-NC and saline groups. The result validates the importance of TLR3 in PIA, however, the ligands and the functional consequences of TLR activation in PIA are not yet fully understood.
TLR3 expresses mainly on DC for humans but on macrophages for mice . It has been found that macrophages are involved in the pathology of K/BxN serum-induced arthritis . Macrophage-derived reactive oxygen species (ROS) participate in T cell selection, maturation and differentiation, and also mediate protection against arthritis by suppressing T cell activation . In addition, macrophages stimulated by excessive interleukin-15 may activate the characteristic autoreactive CD4+ T cells in RA . The increased macrophage activation may be mediated by TLRs in RA or other autoimmune inflammatory diseases [16, 52]. All findings indicate macrophages are a main player in the development of arthritis. We found that TLR3 positive macrophages were increased in the spleen of PIA rats, and cell surface TLR3 showed high expression in the initiation stage of arthritis. It suggests that cell surface TLR3 on macrophage, but not the intracellular expression, exerts a crucial influence on the pathogenesis of PIA.
Using a rat macrophage cell line, NR8383, we could confirm that TLR3, but not TLR4, was upregulated after stimulation with pristane, which excludes LPS contamination in the experiment. Furthermore, the mRNA expression of IFN-β, the main downstream cytokine of TLR3, also increased with the same tendency as that of TLR3. The increase of IFN-β and TNF-α was inhibited by anti-TLR3 antibody, suggesting that this induction was TLR3 dependent. The above mentioned data indicate TLR3 and its downstream molecules in macrophage were activated by pristane, and then took part in the pathogenesis of PIA. More TLR3 expression on macrophages could affect the cell function, such as the capacity of antigen presentation, ROS production, phagocytosis, secretion of cytokines and chemokines and so on. Macrophages with upregulated TLR3 may affect the balance of Th1/Th2 and the activations of autoreactive T cells and B cells [25, 42].
However, it is still unclear how pristane induces TLR3 expression. The interaction between TLR and alkanes like pristane is not completely known. It is reported that oxidized alkane polymers induced activation of the TLR1/2 pathway as its ligands. And pristane could augment the effect of TLR7 ligands but does not directly activate TLR7. In a PIA rat model, further study is needed as to whether pristane or its metabolism products are the ligand of TLR3, or if it induces TLR3 by another pathway. Further studies are also needed to understand underlying mechanisms as to how TLR3 activates joint-specific autoimmune T cells via macrophages.
In summary, we screened TLR and downstream cytokine expression in the spleen of PIA rats, and found that only TLR3 expression was increased at the initiation stage. Regulating TLR3 by using ligand or shRNA in vivo could directly aggravate or relieve symptoms of arthritis. TLR3 may play its role via splenic macrophage, since it had a high expression on macrophages after pristane injection in vivo. And the induction of TLR3 was specifically due to pristane stimulation in macrophage cell lines with a dose- and time- dependent manner. These findings are not only useful in understanding the underlying pathogenesis of RA, but also provide a valuable clue for other immunological disease research.
fluorescence-activated cell sorting
fibroblast like synoviocyte
mean fluorescence intensity
phosphate buffered saline
C: polyinosine-polycytidylic acid
reactive oxygen species
tumor necrosis factor alpha.
Firestein GS: Evolving concepts of rheumatoid arthritis. Nature. 2003, 423: 356-361. 10.1038/nature01661.
Arend WP: The innate immune system in rheumatoid arthritis. Arthritis Rheum. 2001, 44: 2224-2234. 10.1002/1529-0131(200110)44:10<2224::AID-ART384>3.0.CO;2-H.
Ji H, Ohmura K, Mahmood U, Lee DM, Hofhuis FM, Boackle SA, Takahashi K, Holers VM, Walport M, Gerard C, Ezekowitz A, Carroll MC, Brenner M, Weissleder R, Verbeek JS, Duchatelle V, Degott C, Benoist C, Mathis D: Arthritis critically dependent on innate immune system players. Immunity. 2002, 16: 157-168. 10.1016/S1074-7613(02)00275-3.
O'Neill LA: Primer: Toll-like receptor signaling pathways - what do rheumatologists need to know?. Nature Clinical Practice Rheumatology. 2008, 4: 319-327. 10.1038/ncprheum0802.
Trinchieri G, Sher A: Cooperation of Toll-like receptor signals in innate immune defence. Nature Reviews Immunology. 2007, 7: 179-190. 10.1038/nri2038.
Yrlid U, Milling SW, Miller JL, Cartland S, Jenkins CD, MacPherson GG: Regulation of intestinal dendritic cell migration and activation by plasmacytoid dendritic cells, TNF-alpha and type 1 IFNs after feeding a TLR7/8 ligand. J Immunol. 2006, 176: 5205-5212.
Chan CW, Crafton E, Fan HN, Flook J, Yoshimura K, Skarica M, Brockstedt D, Dubensky TW, Stins MF, Lanier LL, Pardoll DM, Housseau F: Interferon-producing killer dendritic cells provide a link between innate and adaptive immunity. Nature Medicine. 2006, 12: 207-213. 10.1038/nm1352.
Abdollahi-Roodsaz S, Joosten LAB, Koenders MI, Devesa I, Roelofs MF, Radstake T, Heuvelmans-Jacobs M, Akira S, Nicklin MJH, Ribeiro-Dias F, Van den Berg WB: Stimulation of TLR2 and TLR4 differentially skews the balance of T cells in a mouse model of arthritis. Journal of Clinical Investigation. 2008, 118: 205-216. 10.1172/JCI32639.
Abe M, Tokita D, Raimondi G, Thomson AW: Endotoxin modulates the capacity of CpG-activated liver myeloid DC to direct Th1-type responses. European Journal of Immunology. 2006, 36: 2483-2493. 10.1002/eji.200535767.
Liu HY, Komai-Koma M, Xu D, Liew FY: Toll-like receptor 2 signaling modulates the functions of CD4(+)CD25(+) regulatory T cells. Proceedings of the National Academy of Sciences of the United States of America. 2006, 103: 7048-7053. 10.1073/pnas.0601554103.
Sutmuller RPM, den Brok M, Kramer M, Bennink EJ, Toonen LWJ, Kullberg BJ, Joosten LA, Akira S, Netea MG, Adema GJ: Toll-like receptor 2 controls expansion and function of regulatory T cells. Journal of Clinical Investigation. 2006, 116: 485-494. 10.1172/JCI25439.
Roelofs MF, Joosten LA, Abdollahi-Roodsaz S, van Lieshout AW, Sprong T, van den Hoogen FH, van den Berg WB, Radstake T: The Expression of toll-like receptors 3 and 7 in rheumatoid arthritis synovium is increased and costimulation of toll-like receptors 3, 4, and 7/8 results in synergistic cytokine production by dendritic cells. Arthritis Rheum. 2005, 52: 2313-2322. 10.1002/art.21278.
Ospelt C, Brentano F, Rengel Y, Stanczyk J, Kolling C, Tak PP, Gay RE, Gay S, Kyburz D: Overexpression of toll-like receptors 3 and 4 in synovial tissue from patients with early rheumatoid arthritis toll-like receptor expression in early and longstanding arthritis. Arthritis Rheum. 2008, 58: 3684-3692. 10.1002/art.24140.
Brentano FS, Gay O, Gay RE, Kyburz S: RNA released from necrotic synovial fluid cells activates rheumatoid arthritis synovial fibroblasts via Toll-like receptor 3. Arthritis Rheum. 2005, 52: 2656-2665. 10.1002/art.21273.
Seibl R, Birchler T, Loeliger S, Hossle JP, Gay RE, Saurenmann T, Michel BA, Seger RA, Gay S, Lauener RP: Expression and regulation of toll-like receptor 2 in rheumatoid arthritis synovium. American Journal of Pathology. 2003, 162: 1221-1227.
Huang QQ, Ma YY, Adebayo A, Pope RM: Increased macrophage activation mediated through toll-like receptors in rheumatoid arthritis. Arthritis Rheum. 2007, 56: 2192-2201. 10.1002/art.22707.
van der Heijden IM, Wilbrink B, Tchetverikov I, Schrijver IA, Schouls LM, Hazenberg MP, Breedveld FC, Tak PP: Presence of bacterial DNA and bacterial peptidoglycans in joints of patients with rheumatoid arthritis and other arthritides. Arthritis Rheum. 2000, 43: 593-598. 10.1002/1529-0131(200003)43:3<593::AID-ANR16>3.0.CO;2-1.
Roelofs MF, Boelens WC, Joosten LA, Abdollahi-Roodsaz S, Geurts J, Wunderink LU, Schreurs BW, van den Berg WB, Radstake T: Identification of small heat shock protein B8 (HSP22) as a novel TLR4 ligand and potential involvement in the pathogenesis of rheumatoid arthritis. J Immunol. 2006, 176: 7021-7027.
Iwahashi M, Yamamura M, Aita T, Okamoto A, Ueno A, Ogawa N, Akashi S, Miyake K, Godowski PJ, Makino F: Expression of toll-like receptor 2 on CD16+ blood monocytes and synovial tissue macrophages in rheumatoid arthritis. Arthritis Rheum. 2004, 50: 1457-1467. 10.1002/art.20219.
Gutierrez-Canas I, Juarranz Y, Santiago B, Arranz A, Martinez C, Galindo M, Paya M, Gomariz RP, Pablos JL: VIP down-regulates TLR4 expression and TLR4-mediated chemokine production in human rheumatoid synovial fibroblasts. Rheumatology. 2006, 45: 527-532. 10.1093/rheumatology/kei219.
Kyburz D, Rethage J, Seibl R, Lauener R, Gay RE, Carson DA, Gay S: Bacterial peptidoglycans but not CpG oligodeoxynucleotides activate synovial fibroblasts by toll-like receptor signaling. Arthritis Rheum. 2003, 48: 642-650. 10.1002/art.10848.
Cho ML, Ju JH, Kim HR, Oh HJ, Kang CM, Jhun JY, Lee SY, Park MK, Min JK, Park SH, Lee SH, Kim HY: Toll-like receptor 2 ligand mediates the upregulation of angiogenic factor, vascular endothelial growth factor and interleukin-8 CXCL8 in human rheumatoid synovial fibroblasts. Immunology Letters. 2007, 108: 121-128. 10.1016/j.imlet.2006.11.005.
Jung YO, Cho ML, Kang CM, Jhun JY, Park JS, Oh HJ, Min JK, Park SH, Kim HY: Toll-like receptor 2 and 4 combination engagement upregulate IL-15 synergistically in human rheumatoid synovial fibroblasts. Immunology Letters. 2007, 109: 21-27. 10.1016/j.imlet.2006.12.006.
Pierer M, Rethage J, Seibl R, Lauener R, Brentano F, Wagner U, Hantzschel H, Michel BA, Gay RE, Gay S, Kyburz D: Chemokine secretion of rheumatoid arthritis synovial fibroblasts stimulated by toll-like receptor 2 ligands. J Immunol. 2004, 172: 1256-1265.
Herlands RA, Christensen SR, Sweet RA, Hershberg U, Shlomchik MJ: T cell-independent and toll-like receptor-dependent antigen-driven activation of autoreactive B cells. Immunity. 2008, 29: 249-260. 10.1016/j.immuni.2008.06.009.
Isnardi I, Ng YS, Srdanovic I, Motaghedi R, Rudchenko S, von Bernuth H, Zhang SY, Puel A, Jouanguy E, Picard C, Garty BZ, Camcioglu Y, Doffinger R, Kumararatne D, Davies G, Gallin JI, Haraguchi S, Day NK, Casanova JL, Meffre E: IRAK-4-and MyD88-Dependent Pathways Are Essential for the Removal of Developing Autoreactive B Cells in Humans. Immunity. 2008, 29: 746-757. 10.1016/j.immuni.2008.09.015.
Rueckert R, Brandt K, Ernst M, Marienfeld K, Csernok E, Metzler C, Budagian V, Bulanova E, Paus R, Bulfone-Paus S: Interleukin-15 stimulates macrophages to activate CD4(+) T cells: a role in the pathogenesis of rheumatoid arthritis?. Immunology. 2009, 126: 63-73. 10.1111/j.1365-2567.2008.02878.x.
Liu ZQ, Deng GM, Foster S, Tarkowski A: Staphylococcal peptidoglycans induce arthritis. Arthritis Research. 2001, 3: 375-380. 10.1186/ar330.
Deng GM, Nilsson IM, Verdrengh M, Collins LV, Tarkowski A: Intra-articularly localized bacterial DNA containing CpG motifs induces arthritis. Nature Medicine. 1999, 5: 702-705. 10.1038/9554.
Abdollahi-Roodsaz S, Joosten LA, Helsen MM, Walgreen B, van Lent PL, van den Bersselaar LA, Koenders MI, van den Berg WB: Shift From Toll-like Receptor 2 (TLR-2) Toward TLR-4 Dependency in the Erosive Stage of Chronic Streptococcal Cell Wall Arthritis Coincident With TLR-4-Mediated Interleukin-17 Production. Arthritis Rheum. 2008, 58: 3753-3764. 10.1002/art.24127.
Joosten LA, Koenders MI, Smeets RL, Heuvelmans-Jacobs M, Helsen MM, Takeda K, Akira S, Lubberts E, van de Loo FA, van den Berg WB: Toll-like receptor 2 pathway drives streptococcal cell wall-induced joint inflammation: Critical role of myeloid differentiation factor 88. J Immunol. 2003, 171: 6145-6153.
Lee EK, Kang SM, Paik DJ, Kim JM, Youn J: Essential roles of Toll-like receptor-4 signaling in arthritis induced by type II collagen antibody and LPS. International Immunology. 2005, 17: 325-333. 10.1093/intimm/dxh212.
Choe JY, Crain B, Wu SR, Corr M: Interleukin 1 receptor dependence of serum transferred arthritis can be circumvented by toll-like receptor 4 signaling. Journal of Experimental Medicine. 2003, 197: 537-542. 10.1084/jem.20021850.
Asagiri M, Hirai T, Kunigami T, Kamano S, Gober HJ, Okamoto K, Nishikawa K, Latz E, Golenbock DT, Aoki K, Ohya K, Imai Y, Morishita Y, Miyazono K, Kato S, Saftig P, Takayanagi H: Cathepsin K-dependent Toll-like receptor 9 signaling revealed in experimental arthritis. Science. 2008, 319: 624-627. 10.1126/science.1150110.
Vingsbo C, Sahlstrand P, Brun JG, Jonsson R, Saxne T, Holmdahl R: Pristane-induced arthritis in rats - A new model for rheumatoid arthritis with a chronic disease course influenced by both major histocompatibility complex and non-major histocompatibility complex genes. American Journal of Pathology. 1996, 149: 1675-1683.
Olofsson P, Holmberg J, Tordsson J, Lu SM, Akerstrom B, Holmdahl R: Positional identification of Ncf1 as a gene that regulates arthritis severity in rats. Nature Genetics. 2003, 33: 25-32. 10.1038/ng1058.
Dedera DA, Urashima M, Chauhan D, LeBrun DP, Bronson RT, Anderson KC: Interleukin-6 is required for pristane-induced plasma cell hyperplasia in mice. British Journal of Haematology. 1996, 94: 53-61. 10.1046/j.1365-2141.1996.6282074.x.
Wolf NA, Amouzegar TK, Swanborg RH: Synergistic interaction between Toll-like receptor agonists is required for induction of experimental autoimmune encephalomyelitis in Lewis rats. Journal of Neuroimmunology. 2007, 185: 115-122. 10.1016/j.jneuroim.2007.02.001.
Okamoto S, Matsuura M, Akagi T, Akashi M, Tanimoto T, Ishikawa T, Takahashi M, Yamanishi K, Mori Y: Poly(gamma-glutamic acid) nano-particles combined with mucosal influenza virus hemagglutinin vaccine protects against influenza virus infection in mice. Vaccine. 2009, 27: 5896-5905. 10.1016/j.vaccine.2009.07.037.
Filleur S, Courtin A, Ait-Si-Ali S, Guglielmi J, Merle C, Harel-Bellan A, Clezardin P, Cabon F: SiRNA-mediated inhibition of vascular endothelial growth factor severely limits tumor resistance to Antiangiogenic thrombospondin-1 and slows tumor vascularization and growth. Cancer Research. 2003, 63: 3919-3922.
Spankuch B, Matthess Y, Knecht R, Zimmer B, Kaufmann M, Strebhardt K: Cancer inhibition in nude mice after systemic application of U6 promoter-driven short hairpin RNAs against PLK1. Journal of the National Cancer Institute. 2004, 96: 862-872. 10.1093/jnci/djh146.
Holmberg J, Tuncel J, Yamada H, Lu SM, Olofsson P, Holmdahl R: Pristane, a non-antigenic adjuvant, induces MHC class II-restricted, arthritogenic T cells in the rat. J Immunol. 2006, 176: 1172-1179.
Hoffmann MH, Tuncel J, Skriner K, Tohidast-Akrad M, Tuerk B, Pinol-Roma S, Serre G, Schett G, Smolen JS, Holmdahl R, Steiner G: The rheumatoid arthritis-associated autoantigen hnRNP-A2 (RA33) is a major stimulator of autoimmunity in rats with pristane-induced arthritis. J Immunol. 2007, 179: 7568-7576.
Kleinau S, Dencker L, Klareskog L: Oil-induced arthritis in DA rats - tissue distribution of arthritogenic 14C-labeled hexadecane. International Journal of Immunopharmacology. 1995, 17: 393-401. 10.1016/0192-0561(95)00020-3.
Olofsson P, Nerstedt A, Hultqvist M, Nilsson EC, Andersson S, Bergelin A, Holmdahl R: Arthritis suppression by NADPH activation operates through an interferon-β pathway. BMC Biology. 2007, 5: 19-10.1186/1741-7007-5-19.
Mao F, Xu W-R, Qian H, Zhu W, Yan Y-M, Gao S, Xu H-X: [The expression of Toll-like receptor 8 and cytokines in rheumatoid arthritis mice induced by chicken II collogen]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2009, 25: 312-314.
Barton GM, Medzhitov R: Toll-like receptor signaling pathways. Science. 2003, 300: 1524-1525. 10.1126/science.1085536.
Yaron M, Baratz M, Yaron I, Zor U: Acute Induction of Joint Inflammation in the Rat by Poly-I.Poly-C. Inflammation. 1979, 3: 243-251. 10.1007/BF00914181.
Heinz S, Haehnel V, Karaghiosoff M, Schwarzfischer L, Muller M, Krause SW, Rehli M: Species-specific regulation of Toll-like receptor 3 genes in men and mice. Journal of Biological Chemistry. 2003, 278: 21502-21509. 10.1074/jbc.M301476200.
Solomon S, Rajasekaran N, Jeisy-Walder E, Snapper SB, Illges H: A crucial role for macrophages in the pathology of K/B × N serum-induced arthritis. European Journal of Immunology. 2005, 35: 3064-3073. 10.1002/eji.200526167.
Gelderman KA, Hultqvist M, Pizzolla A, Zhao M, Nandakumar KS, Mattsson R, Holmdahl R: Macrophages suppress T cell responses and arthritis development in mice by producing reactive oxygen species. Journal of Clinical Investigation. 2007, 117: 3020-3028. 10.1172/JCI31935.
Hu XY, Chakravarty SD, Ivashkiv LB: Regulation of interferon and Toll-like receptor signaling during macrophage activation by opposing feedforward and feedback inhibition mechanisms. Immunological Reviews. 2008, 226: 41-56. 10.1111/j.1600-065X.2008.00707.x.
We should express gratitude to Prof. Yili Wang and Xu Li for critical reading the manuscript. And we are also grateful to Mr. Fujun Zhang, Ms. Yan Han and Qilan Ning for their expertise and assistance in the experiments. The work was supported by grants from the National Natural Science Foundation of China (30801027 and 30630058) and Shaanxi Province International Cooperation Foundation of China (2007-KW-06).
The authors declare that they have no competing interests.
LM, WZ, SL and RH conceived and designed the experiments. LM and WZ performed the experiments and analyzed the data. CJ and XH performed some experiments. WH and FZ prepared reagents. LM, WZ, RH and SL had extensive scientific discussion for this study and wrote the paper. All authors read and approved the final manuscript.
Liesu Meng, Wenhua Zhu contributed equally to this work.
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Meng, L., Zhu, W., Jiang, C. et al. Toll-like receptor 3 upregulation in macrophages participates in the initiation and maintenance of pristane-induced arthritis in rats. Arthritis Res Ther 12, R103 (2010). https://doi.org/10.1186/ar3034
- Rheumatoid Arthritis
- Saline Group
- TLR3 Expression