Objective Animal models for human diseases are especially valuable for clarifying molecular mechanisms before or around the onset. As a model for rheumatoid arthritis (RA), we utilise knock-in mice gp130F759. They have a Y759F mutation in gp130, a common receptor subunit for interleukin 6 (IL-6) family cytokines. Definitive arthritis develops around 8 months old and the incidence reaches 100% around 1 year old. Careful examination in the clinical course revealed very subtle resistance in flexibility of joints at 5 months old. Therefore, pathophysiological changes in gp130F759 were examined to dissect molecular mechanisms for preclinical phase of RA.
Methods Severity of arthritis in gp130F759 was evaluated with a clinical score system and histological quantification. Serum cytokines, autoantibodies and C reactive protein (CRP) were measured. Changes in the synovium were analysed by real-time PCR, flow cytometry and immunohistochemistry.
Results Around 5 months old, various types of cytokines, rheumatoid factor (RF), anti-circular citrullinated peptide IgM and CRP increased in the sera of gp130F759. Enhancement of neovascularisation, synovial hyperplasia and fibrosis was observed. Also, increases in haematopoietic cells dominated by innate immune cells and gene expression of Il6 and Padi4 were detected in the joints. Il6 was expressed by non-haematopoietic synovial cells, whereas PAD4 protein was detected in the synovial neutrophils. Padi4 is induced in neutrophils in vitro by IL-6. Increases of phospho-STAT3 and PAD4 protein were detected in the synovium. Deletion of IL-6 in gp130F759 normalised the amount of PAD4 protein in the joints.
Conclusion The IL-6-PAD4 axis operates in the earliest phase of arthritis in gp130F759, implicating it in early RA.
- early rheumatoid arthritis
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What is already known about this subject?
Mutant gp130 knock-in mice gp130F759 are a model for rheumatoid arthritis (RA) where a point mutation of gp130 causes aberrant STAT3 activation.
What does this study add?
The earliest time point was identified when the pathological changes common to human RA start in joints of gp130F759 mice.
IL-6 dependent PAD4 production ‘the IL-6-PAD4 axis’, occurs in synovial neutrophils in the preclinical phase of arthritis in gp130F759 mice.
How might this impact on clinical practice?
The gp130F759 model can now be used to probe very early stages of arthritis, seek novel therapeutic targets and devise new treatment strategies.
Rheumatoid arthritis (RA) is an autoimmune disease with 0.3%–1.5% morbidity. It is characterised by chronic, proliferative synovitis with bone erosion leading to joint destruction. Genetic factors (HLA-DRB1, PTPN22 and PADI4 genes, etc), as well as environmental factors (smoking and infection) are involved in breakdown of self-tolerance and activation of autoimmunity.
Critical findings in the understanding and treatment of RA are anti-citrullinated peptide autoantibodies (ACPAs) as specific for RA and effectiveness of anti-cytokine therapies. Development of biologics against TNFα or IL-6 has drastically changed the prognosis of RA and therapeutic strategies. Since serum ACPAs are detected much earlier than the onset of RA,1–3 anti-circular citrullinated peptide (CCP) antibody was included in the criteria for RA of The European League against Rheumatism/American College of Rheumatology (EULAR/ACR) 2010.4 This permit earlier therapeutic application of biologics and the possibility of complete cures for this disease. Recent investigation of RA has proposed a stepwise, progressive model of RA.5–8 But it is difficult to obtain information on the molecular events in the synovium during preclinical phases of RA. This limitation can be partly overcome by the study of animal models.
Citrullination of arginine is catalysed by peptidyl arginine deiminases (PADs),9 which results in generation of modified self-antigens and production of ACPA. PADI4 is one of the risk factors of RA identified by Genome Wide Association Study (GWAS).10 Single nucleotide polymorphisms (SNPs) of PADI4 is responsible for increased expression of PADI4, and deletion of Padi4 in mice ameliorated collagen-induced or anti-G6PI-induced arthritis.11 12 PAD4 mediates autoantibody production and inflammatory arthritis downstream of TNFα.13 However, molecular mechanisms for expression of PADI4 before the clinical onset of RA are poorly understood.
IL-6 is a multifunctional cytokine that regulates the development and functions of neuronal, haematological, inflammatory and immunological systems. Dysregulation of IL-6 is involved in various autoimmune diseases including RA.14 IL-6 receptor complex consists of an IL-6 receptor α chain and a signal transducing subunit gp130. Gp130 is a common receptor subunit for the IL-6 family cytokines, transducing signals through two independent pathways, YXXQ/STAT3 and Y759/SHP2 pathways.15 Gp130F759 knock-in mice have a mutation of tyrosine to phenylalanine at the 759th amino acid residue, and a defect in the negative regulatory pathway by SOCS3. In turn, this leads to prolonged activation of STAT3 by physiological ligands.16 Aberrant activation of STAT3 results in splenomegaly, lymphadenopathy, hyper-γ globulinaemia, auto-antibody production and RA-like arthritis with age.17 Gp130F759 is unique as providing evidence that one amino acid mutation in a cytokine receptor can cause an autoimmune disease. The development of arthritis in gp130F759 is Rag2-dependent, but the Y759F mutation in non-haematopoietic cells is sufficient.17 Several pathophysiological mechanisms have been reported. Homeostatic proliferation of CD4+ T cells driven by IL-6/STAT3-dependent IL-7 production by non-haematopoietic cells,18 IL-6-dependent acceleration of arthritis by transgene of HTLV-1 pX19, triggering effects of polyclonal, antigen-non-specific Th17 accumulated in the joints,20 and a positive feedback loop of IL-6/IL-17A in chronic inflammation.21 From these studies, a four-step model was proposed that explains the mechanism for tissue specific autoimmune diseases by antigen-non-specific activation of the IL-6 amplifier.22 This intriguing model is based on the experiments utilising artificial manipulations, such as neonatal thymectomy,18 puncture or injection of chemokine to the joints20 and over-expression of cytokines by plasmid injection.21 Arthritis of gp130F759 is characterised by late onset around 8 months old, equivalent to the predilection age of human RA, and gradually progresses. Therefore, we have exploited this model to learn that the IL-6-PAD4 axis is operative among early RA related changes.
Materials and methods
All mice in C57BL/6 background were maintained under specific pathogen free (SPF) condition in the animal facility in Kawasaki Medical School Central Research Institute. Gp130F759 is used as a notation for homotypic knock-in mice gp130F759/F75916 17 in this paper. Gp130F759 was crossed with Il6 knockout mouse (Il6KO)23 to make double mutant Il6KO/gp130F759. The animal protocol for this experiment was approved by the Animal Care and Use Committee of Kawasaki Medical School.
Scoring of arthritis
The score system for arthritis from 0 to 4 points/a limb is based on the degree of restriction of joint flexibility (0, no restriction; 1, slight; 2, moderate; 3, severe), and +1 point for redness or swelling for a joint of each fore-limb and hind-limb (online supplementary figure 1). Two researchers who are not informed about genotype scored independently.
Concentration of serum cytokines from gp130F759 (n=12) and wild type (WT) (n=8) were measured using Bio-Plex (Bio-rad, Hercules, California, USA). IL-6 and TNFα in culture supernatant of fibroblast-like synoviocytes were measured with ELISA kits for these cytokines (BioLegend, San Diego, California, USA) following manufacturers instruction.
Neutralising antibody for IL-6
Rat anti-IL-6 monoclonal antibodies (mAb) (IgG1; clone #MP5-20F3) and isotype matched control mAb were purchased from BioLegend and Zymed (San Francisco, California, USA), respectively.
Quantitative histology for arthritis
Ankle containing synovium was fixed in 10% neutral buffered formalin, decalcified with 10% formic acid and embedded in paraffin. Sliced tissue was stained with HE. For estimation of fibrosis, sliced tissue was stained with Sirius red F3BA (WALDECK, Münster, Germany). Using Image J software available on the web site, histological changes in preclinical to very early arthritis were quantitatively estimated using criteria as follows (figure 2B): For neovascularisation, the numbers of the transverse section typical for newly formed vasculature (black arrow) in the total region of synovium (light green lined) were counted. Hyperplasia was defined by synovial lining that has four cell-layers or more, and evaluated with a formula (the length of lining with hyperplasia (yellow line)/length of total synovial lining (blue line))×100 (%). For fibrosis, the ratio of fibrosis (fibrosis area positively stained with Sirius red/total area of synovium (light green lined))×100 (%) was calculated by Image J software.
Splenocytes were prepared by teasing the spleen with slide glasses. The synovium of the knee joint was dissected with scalpel, minced and digested with collagenase D (Roche Diagnostics, Mannheim, Germany) for 3 hours at 37°C in CO2 incubator. After washing and passing through mesh, synovial cells were used for flowcytometry.
Synovial cells were separated to CD45+ haematopoietic and CD45− non-haematopoietic cells using rat anti-mouse CD45 mAb (BD Biosciences) and magnetic beads coupled with sheep anti-rat IgG (H+L) (Thermo Fisher Scientific,Waltham, MA). Real-time PCR detected no transcripts for Cd45 in the cDNA prepared from CD45− fractions. Cultured for 3 days in MEMα containing 15% Fetal calf serum (FCS) and penicillin/streptomycin, CD45− fractions showed typical morphology for fibroblasts, indicating that synovial CD45− fractions are compatible with fibroblast-like synoviocytes.
Bone marrow neutrophils were purified with neutrophil separation kit (Miltenyi Biotech, Bergisch Gladbach, Germany) using MACS LS column. Purities of neutrophils (CD11b+Gr-1hi) confirmed with FACSCanto II were usually more than 98%. Neutrophils were stimulated with various concentrations of human rIL-6 (2–100 ng/mL), LPS (E. coli 0111:B4) (Sigma-Aldrich, St. Louis, Missouri, USA), or culture supernatant fluid of CD45− synovial cells for 6 hours. After each separation or incubation, the cells were collected into TRIzol (Thermo Fisher Scientific) and store at −80°C until use.
Flow cytometry and typing of synovial cells
Splenocytes and synoviocytes were blocked with mixture of supernatant of anti-CD16/32 mAb (2.4G2) and 5% heat inactivated rat serum. Then the cells were stained with two sets of cocktail mAbs labelled with fluorescent dyes. Set 1 consists of FITC-anti-Ly-6G/Ly-6C (Gr-1) (RB6-8C5) (BD biosciences), PE-anti-CD3ε (145-2C11) (Tonbo Bioscience, Burlingame, California, USA), PE-Cy7-anti-TER119, APC-anti-CD11c (N418), APC-Cy7-anti-CD19 (6D5) (BioLegend), eFlour450-anti-CD4 (GK1.5) (Tonbo Bioscience) mAbs. Set 2 consists of PerCP-Cy5.5-labelled anti-CD3ε, -CD19, -NK1.1 (PK136) (Tonbo Bioscience), -TER119 (eBioscience, San Diego, California, USA), PE-SiglecF (BD Biosciences), APC-F4/80 (eBioscience), APC-Cy7-Gr-1 and Pacific Blue-CD11b (BioLegend). The stained samples were analysed with FACSCanto II with FACSDiva software (BD Biosciences). Details to define cellular subsets are indicated in online supplementary figure 2. Cells were suspended in 0.4% Trypan Blue and total viable cell numbers were counted using Bürker-Türk haemocytometer under a microscope. With total viable cell numbers and frequencies obtained by flowcytometry (online supplementary figure 3), the cell numbers of a certain cell-lineage in the spleen or synovium were calculated.
The protocol of anti-CCP ELISA (MESA CUP-2 test, MBL, Nagoya, Japan) was adapted for mouse serum using goat anti-mouse IgM or IgG antibodies-labelled with alkaline phosphatase (SouthernBiothech, Birmingham, Alabama, USA) as secondary antibodies. ELISA kits for mouse C reactive protein (CRP) (Helica Biosystems, Santa Ana, California, USA) and mouse RF (IgM) (FUJIFILM Wako Shibayagi, Gunma, Japan) were used according to the manufacturer’s instructions.
Quantitative real-time RT-PCR
Total RNAs were extracted with TRIzol. Random hexamer-primed cDNAs were prepared using ReverTra Ace qPCR RT Kit (TOYOBO, Osaka, Japan). Specific primers for each gene were designed using Universal Primer Design Tools available on the web site of Roche Company. Real-time PCR with the SYBR Green I dye was carried out by the 7300 Real-Time PCR System (Thermo Fisher Scientific). Expression levels of target cDNAs were normalised to the endogenous transcription levels of murine Actb.
Lysates of the joints were prepared in TNE lysis buffer (10mM Tris, 150mM NaCl, 1mM EDTA with 1% Nonidet-P40) and the 20-µg equivalent whole cell crudes were boiled in sample buffer for 5 min, resolved on Sodium dodecyl sulfate-Poly-Acrylamide Gel Electrophoresis (SDS-PAGE), and transferred electrically onto Immobilon-FL PolyVinylidene DiFluoride (PVDF) membrane (Merck Millipore, Darmstadt, Germany). After blocking with fish gelatin, the membrane was incubated with rabbit anti-PAD4 antibody (Proteintech Group, Chicago, Illinois, USA), and rabbit anti-phospho-STAT3 (Tyr705) (pSTAT3) antibody (Cell Signaling Technology, Beverly, Massachusetts, USA), for overnight at 4°C. Bound antibodies were visualised with secondary antibody IRDye 800CW-labelled donkey anti-rabbit IgG (LI-COR, Lincoln, Nebraska, USA) with Odyssey CLx (LI-COR). Anti-pSTAT3 antibody was stripped with Western BLoT Stripping Buffer (TAKARA Bio, Shiga, Japan), and then the membrane was reprobed with rabbit anti-STAT3 antibody (Cell Signaling Technology).
Ankle sections were made by Kawamoto’s film method24 using cryofilm type 2 (Section-Lab Co, Hiroshima, Japan). The sections were fixed with cold-acetone, blocked with Phosphate buffered saline (PBS) containing 5% donkey serum, 2% FCS and 0.09% NaN3, and then incubated with rabbit anti-mouse PAD4 or anti-pSTAT3 with Can Get Signal immunostain buffer A (TOYOBO) for 2 hours at room temperature. After washed, secondary antibodies Cy3-labelled F(ab’)2 donkey anti-rabbit IgG (H+L) (Jackson ImmunoResearch, West Grove, Pennsylvania, USA) with Hoechst 33342 were incubated for 30 min at room temperature. For studying colocalisation, sections were first stained with rabbit anti-PAD4 antibody and Cy3-labelled F(ab’)2 donkey anti-rabbit IgG (H+L). The sections were blocked with 5% rabbit serum, washed and then stained with biotinylated rabbit anti-pSTAT3 (Tyr705) monoclonal antibody (Cell Signaling Technology) and DyLight488-streptavidin (Vector Laboratories, Burlingame, California, USA). Sections were mounted with VECTASHIELD (Vector Laboratories), scanned with LSM700 confocal microscope (ZEISS, Jena, Germany) and analysed with Zen (ZEISS).
For preparation of cytospin slides, synovial cells were centrifuged onto slide glass with Shandon Cytospin III (Thermo Fisher Scientific) and air-dried immediately.
Serum concentrations of cytokines, autoantibodies and CRP, cell numbers, histological and biochemical quantification, and quantity of gene expression, were compared by the Mann-Whitney U test. A part of data was compared by the Kruskal-Wallis test and Dunn’s method was used as post-hoc testing. Data were analysed using GraphPad Prism8 (GraphPad Software Inc., San-Diego, CA).
Earliest pathological changes in gp130F759 mice develop at 5 months old
We re-evaluated the clinical course of arthritis in gp130F759 under SPF conditions using a scoring system described in Methods section and online supplementary figure 1. As reported previously,17 obvious restriction of joint flexibility appeared at 8 months old. This gradually increased in degree, leading to ankylosis. The incidence of clinical arthritis was 50% at 11 months old and reached 100% by 12 months old (figure 1A). There were no sex differences in the age of onset, progress and incidence of arthritis.
First, we examined the relationships between clinical scores and histological changes of ankle joint specimens stained with HE and Sirius red (figure 1B and 1C). Joint specimens in a group with sum of the scores 3 showed significant changes such as thickening of the synovial lining, and replacement of adipocytes by fibroblasts, and neovascularisation. At score 5, cellular infiltration increased. In mice with scores of 0, there were apparently no changes in gp130F759 compared with WT. These data indicate that our scoring system for clinical arthritis reflects histological changes of the joints.
To clarify the earliest changes in joints developing arthritis, we focused on the age around 5 months old, when very faint resistance in the flexibility of the ankle joints was perceived. Bio-Plex analysis of serum cytokines revealed increases in various cytokines including inflammatory (TNFα, IL-1β, IL-6, IL-17), anti-inflammatory (IL-10), Th1 (IL-12, IFNγ) and Th2 (IL-4, IL-13) cytokines (figure 2A). However, most of these changes were not significant except for IL-6 and there were no obvious histological changes at this age. Therefore, we quantitatively re-evaluated the specimens of hindlimbs from gp130F759 with clinical arthritic scores 0 using criteria indicated in figure 2B. As shown in figure 2B, increased degrees of neovascularisation, hyperplasia and fibrosis were observed in the joints of gp130F759 with clinical arthritic scores 0, indicating that local pathological changes in the joints had already developed. This was further indicated by flow cytometry analyses of synovium, which revealed increases in total cell numbers approximately twofold including neutrophils, macrophages and others in the synovium but not in the spleen (figure 2C, online supplementary figure 3). These results prompted us to examine the sera to obtain data usable for diagnosis of RA. Serum CRP and anti-CCP-IgM significantly increased with non-significant increase of RF-IgM (figure 2D), indicating that gp130F759 at 5 months old could be a model equivalent to preclinical to early phase of human RA. Therefore, we analysed the synovium of gp130F759 mice around 5 months old in more detail.
Padi4 gene expression was increased in the joints of gp130F759
Since serum anti-CCP antibody increased, we examined the expression of Padi family genes by real-time PCR. Expression levels of Padi4, but not Padi1, 2, 3 and 6, were significantly higher in the joints of gp130F759 than those of WT (figure 3A, online supplementary figure 4). Furthermore, expression of Il6 and Osm genes also increased in the joints (figure 3B). This strongly suggests that Padi4 gene expression is induced in the process of local inflammation mediated by neutrophils, which produce OSM. Among the chemokines known to attract neutrophils, expression of Cxcl1, Cxcl2 and Cxcl5 did not increase but that of Cxcl7 significantly increased by 54 times (figure 3B).
Since expression of Padi4 gene was increased in joints of gp130F759, we examined PAD4 protein levels and activation status of STAT3 by western blot analysis. As shown in figure 4A, increases of PAD4 protein and tyrosine-phosphorylation of STAT3 in gp130F759 were clearly demonstrated, suggesting the possible relationship between the local increase of Padi4 expression and abnormally enhanced activation of STAT3 in the joints of gp130F759. To confirm the spatial corelation of STAT3 activation and PAD4 production in the joint microenvironments, immunohistochemical analyses were performed using frozen sections of the joints of gp130F759 at 5 months old. Increased reactivities of anti-PAD4 antibody as well as those of anti-phospho-STAT3 antibody were clearly detectable in gp130F759 (figure 4B). Furthermore, the reactivities of anti-phospho-STAT3 antibody, some of which showed nuclear localisation (inset), were increased in gp130F759. These data clearly demonstrate that aberrant STAT3 activation and PAD4 production take place in the preclinical stage of arthritis in gp130F759. Importantly, very few cells, with frequency approximately two in 340 cells, showed colocalisation of reactivities of anti-phospho-STAT3 antibody and anti-PAD4 antibody (figure 4B, right inset), indicating that a relationship between gp130 signal and PAD4 production is observable in a single cell level.
Then, we investigated cells expressing Padi4 in the joints. In the synovia of gp130F759, Padi4 gene was highly expressed selectively by haematopoietic cells (figure 4C). Interestingly, increased expression of Il6 gene was observed in non-haematopoietic synovial cells in gp130F759. Actually, ELISA revealed increased production of IL-6 in culture supernatant fluid (CSF) of CD45− synovial cells from gp130F759 compared with that of WT (figure 4D). Next, to characterise the haematopoietic cells expressing PAD4, synovial cells liberated with collagenase treatment were cytospun and stained with anti-PAD4 antibody. Characteristic nuclear morphology of PAD4+ cells indicated that they are neutrophil lineage (figure 4E photo and inset). Numbers of PAD4+ cells were higher in gp130F759 than WT mice (figure 4E graph).
To examine whether the increased expression of Padi4 depends on IL-6, neutrophils enriched from the bone marrow were stimulated with IL-6 (online supplementary figure 5). The expression levels of Padi4 in neutrophils from gp130F759 and WT similarly increased by IL-6 stimulation.
To confirm the interaction between non-haematopoietic synovial cells and neutrophils, we tested whether the CSF from non-haematopoietic synovial cells has activity to induce Padi4 expression in neutrophils. Stimulation with CSF of CD45− synovial cells from gp130F759 induced Padi4 gene expression in WT neutrophils (figure 4F). This Padi4-inducing activity was proved to be mediated mainly by IL-6, because preincubation with anti-IL-6 neutralising antibody but not control antibody inhibited Padi4 gene induction to the basal level. To confirm operation of IL-6 signal in a single cell level, WT neutrophils were incubated with CSF of CD45− synovial cells from gp130F759 for 30 min, cytospun, and stained with rabbit anti-phosph-STAT3 antibody with Cy3 labelled second antibody. Photos in figure 4G clearly indicate that the CSF strongly induced phosphorylation of STAT3, which is inhibited by pretreatment of CSF with anti-IL-6 neutralising antibody but not control IgG1. Thus, from these data, we conclude that Padi4 expression was induced in neutrophils by IL-6 produced from non-haematopoietic synovial cells in the joint microenvironment of gp130F759.
Operation of the IL-6-PAD4 axis in preclinical arthritis
To clarify the causative, in vivo roles for IL-6 in the increases of PAD4 and anti-CCP antibody, IL-6 was deleted by crossing gp130F759 with Il6KO. Complete deletion of Il6 gene in gp130F759 resulted in normalisation of splenomegaly (figure 5A,C), and serum levels of RF and anti-CCP antibodies (figure 5B). Importantly, PAD4 production (figure 5D) and synovial cell numbers (figure 5E) returned to almost normal levels. These data indicate that Padi4 induction in the synovium is IL-6 dependent and that operation of the IL-6-PAD4 axis in vivo at an early preclinical phase of RA-like arthritis in gp130F759 (figure 6).
In this study, we focused on the natural course of RA-like arthritis in gp130F759, and especially on events during the preclinical phase. To understand kinetics of systemic immune or inflammatory responses, we first examined a set of serum cytokines with Bio-Plex. This revealed increases of multiple cytokines at 5 months old, much before the recognition of definitive, clinical arthritis at around 8 months old. In most of the cytokines, levels of increases were less than twofold, and not statistically significant. This is possibly because the initial age and progress of preclinical changes in each mouse are variable in the spontaneous arthritis in gp130F759, which is contrasted with other arthritis models induced by immunisation with type II collagen or antigen. Since this time point, 5 months old, coincides with appearance of very faint resistance of joint flexibility much less than point 1 of the arthritis score, we extended the study around this age.
Increases of CRP, anti-CCP antibody and RF in the sera were detected at 5 months old, suggesting that as far as the laboratory data, gp130F759 around 5 months old is equivalent to fulfil the criteria of RA. Flow cytometrical analyses revealed increases of the haematopoietic cells competent in innate immunity. Although the clinical signs of arthritis were not obvious at 5 months old, quantitative histopathological analyses provided evidence for synovial hyperplasia and neovascularisation, the latter is also characteristic of early RA.25 Thus, it can be said that gp130F759 at 5 months old is a model for the preclinical to early phase of RA when minute pathological changes begin. Gene expression analyses revealed that at this time point, increases of Mmp3 and Il6 started in the joint, indicating that local inflammatory responses had already begun. Importantly, the expression of Padi4 gene among members of Padi gene family was increased selectively in the joint. Increased production of PAD4 protein with increase of STAT3 phosphorylation was confirmed by biochemical as well as immunohistological measurements. The technique for magnetic cell separation revealed the role-sharing by non-haematopoietic cells expressing Il6 and haematopoietic cells expressing Padi4 in the synovial microenvironment. Cytological analyses revealed that PAD4 producing cells are neutrophils and stimulation of IL-6 induced Padi4 gene expression in neutrophils. All of these data suggest that the IL-6-PAD4 axis participates in the preclinical phase of RA-like arthritis in gp130F759. We have verified the operation of the IL-6-PAD4 axis by four facts; increased production of IL-6 in CSF of CD45− synovial cells from gp130F759, induction of STAT3 phosphorylation and Padi4 transcription in WT neutrophils stimulated with the CSF, and both inductions were inhibited by anti-IL-6 neutralising antibody.
In the promoter region of Padi4, presence of conserved binding sites for NF-κB, TATA-ETS-like, AP-1, Krüppel-like factor-6 (KLF-6) and SP1 are reported.26 Lack of typical STAT3 binding elements suggests that STAT3 indirectly activates transcription of Padi4. The transcriptional activator KLF-6 that is induced by gp130/STAT3 signal may play a role in inducing Padi4 transcription as reported in oligodendrocytes.27 Since there is a NF-κB binding site and serum TNFα was slightly increased in gp130F759, there is possibility that Padi4 may be induced by TNFα. But it is not likely in the case of gp130F759 around 5 months old, because increases of Tnf gene expression were not observed in CD45− as well as CD45+ synovial cells, and TNFα was not detectable in culture supernatant fluid of CD45− synovial cells by ELISA (data not shown). These results have clearly indicated the causative role for IL-6 from CD45− synovial cells to induce Padi4 transcription in neutrophils, although it cannot completely rule out possible involvement of other cytokines in vivo.
Although the promoter region of PADI4 is highly conserved among species, TNFα/NF-κB signal in myeloid cells shows positive and negative regulations on Padi4 transcription in mouse and human, respectively.26 It can be said that our data have provided experimental evidences that IL-6 signal can activate Padi4 transcription, which was unpredictable by bioinformatic analyses. Previously, roles for synovial fibroblasts-neutrophil interactions in promoting adaptive immunity in RA was reported.28 Thus, the IL-6-PAD4 axis could be a critical, prerequisite event by synovial fibroblasts-neutrophil interactions to promote transition from innate to adaptive immunity in early RA. It is intriguing to speculate that the molecular mechanism triggering initiation of RA is PADI4 induction in neutrophils by IL-6/STAT3 signalling provided from non-haematopoietic cells, such as fibroblast-like synoviocytes, in the synovial microenvironments (figure 6). This hypothetical mechanism deserves further analyses in human system.
Deletion of IL-6 in gp130F759 was previously found to result only in retardation of the progress and reduction of severity of arthritis. However, the final incidence of disease was unaffected.18 In the preclinical phase of gp130F759 in this study, deletion of IL-6 resulted in the reduction of splenomegaly, CRP, RF, PAD4 production, anti-CCP-IgM and synovial cell numbers, indicating that these parameters are IL-6-dependent and that IL-6 is critically involved in the initiation of synovial hyperplasia.
In addition to novel findings concerning the IL-6-PAD4 axis, serum cytokine profiling also revealed other important characteristics of the preclinical phase that has similarity with RA. First, in the preclinical phase, when the elevation of anti-CCP antibody was detected, systemic, low-level increases of typical inflammatory cytokines, such as TNFα, IL-1β, IL-6 and IL-17 already existed. Second, cytokines that are elevated in this phase showed no deviation to Th1 or Th2, that is, both Th1 and Th2 types were elevated. Third, an immune-suppressive cytokine, IL-10 also increased. None of the changes were specific to this animal model. On the contrary, the pre-clinical phase of gp130F759 has quite similar cytokine profile to the early phase of RA.29–32 Especially, TNFα, IL-1β, IL-10 and IL-13 are cytokines frequently reported in early RA and also detected in our model. As a STAT3-activating cytokine, IL-10 may have a unique role in early RA25 and dysregulation of IL-10 in RA synovial macrophages has been reported.33
Another similarity to RA is induction of a chemokine CXCL7 attracting neutrophils, which was reported to be produced by synovial macrophages in early RA.34 Interestingly, our novel, infection-induced arthritis model using gp130F759 at 3 months old (unpublished observation by Yahagi et al.) revealed that systemic infection of Mycoplasma fermentans induced expression of Cxcl7 and accumulation of cells dominated by neutrophil in the synovium. This suggests intriguing possibility that aberrant cytokine signals and triggering by microorganisms utilise common pathway to initiates arthritis by induction of Cxcl7 and accumulation of neutrophils in gp130F759.
From all the data obtained in this paper, we propose a model for molecular events in the synovial microenvironments of pre-clinical phase of RA. Importantly, the IL-6-PAD4 axis operates to promote the transition from innate immunity to acquired immunity (figure 6). Thus, gp130F759 is useful to learn the molecular mechanisms for heterogenous pathways leading to a clinical entity RA, which shows variable clinical courses and responses to therapies.
We thank Dr M. Kopf for generous gift of Il6KO. We thank Dr P. W. Kincade for critical reviewing the manuscript. We specially thank Mr N. Iwachido, Ms E. Ohtsuki and Ms K. Yamane at Kawasaki Medical School Central Research Institute for excellent technical assistances of histological analyses and confocal microscopy, respectively. We also thank Ms R. Tanaka, Y. Kenmotsu, M. Funatsu and Y. Matsuo for their technical assistance in this study.
Contributors AY, YS and KI contributed to the conception and study design. AY, TS, MT-I, HI and KI acquired and analysed the data. AY, TS, HH, MT-I, HI, YS and KI contributed to interpretation of the data. AY and KI wrote the first version of the manuscript and FT, HA, MI, YM, HI and YS revised it critically. All authors read and approved the final manuscript.
Funding This work was supported by JSPS KAKENHI Grant Numbers JP17K16217 to AY and JP21590448, JP17K08798 to KI. This work was also supported by Research Project Grants from Kawasaki Medical School to AY and KI and The KAWASAKI Foundation for Medical Science & Medical Welfare to AY.
Competing interests HH and YM have received research support from Chugai pharmaceutical Co.
Patient consent for publication Not required.
Ethics approval The study was approved by the Animal Care and Use Committee of Kawasaki Medical School.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement All data relevant to the study are included in the article or uploaded as supplementary information.
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