Abstract
CD4+ regulatory T (Treg) cells and T-helper 17 (Th17) cells have been shown to have important roles in rheumatoid arthritis (RA). In our previous study, it was demonstrated that artesunate was able to alter the Treg/Th17 ratio in patients with RA; however, the underlying mechanisms remain unclear. The present study established a male Sprague Dawley (SD) rat model of type II collagen-induced arthritis (CIA). SD rats were divided into normal control, CIA model and artesunate-treated (5, 10 or 20 mg/kg/day) groups. Treg and Th17 cells were detected in the synovium by immunohistochemical analysis of forkhead/winged helix transcription factor (Foxp3) and interleukin (IL)-17 expression. Subsequently, lymphocytes were extracted from the rat spleens, and the proportions of Treg/Th17 cells were detected by flow cytometry. The results demonstrated that the expression levels of Foxp3 were significantly decreased, and those of IL-17 were significantly increased, in the CIA model group, as compared with the normal control group. The results demonstrated that artesunate decreased the frequency of Th17 cells and increased the frequency of Treg cells in CIA rats in a dose-dependent manner. In conclusion, the present study suggested that artesunate may regulate the Th17/Treg balance by inducing Th17-mediated apoptosis. Therefore, artesunate may be considered a novel therapeutic agent for the treatment of patients with RA.
Keywords: rheumatoid arthritis, artesunate, T helper 17, regulatory T-cells
Introduction
Rheumatoid arthritis (RA) is a chronic disease involving various immune cells, particularly T lymphocytes, such as CD4+ T-helper (Th) cells (1,2). RA is characterized by chronic inflammation of the joints, synovial hyperplasia and abnormal systemic immune responses. The joint damage that underlies the pathogenesis of RA resembles the process of immune-mediated tumor destruction (3). The formation of blood vessels and degradation of the extracellular matrix are crucial steps in the process of erosion, and T lymphocytes have an important role in these coronary events (4).
CD4+ T cells may differentiate into various lineages that are characterized by their profiles of secreted cytokines. CD4+ regulatory T (Treg) cells and Th17 cells have been described as two original subsets that are distinct from Th1 and Th2 cells. Treg cells, which are characterized by the expression of forkhead/winged helix transcription factor (Foxp3), are essential for regulating self-tolerance and have exhibited anti-inflammatory functions via contact-dependent suppression or by the release of anti-inflammatory cytokines (5). A lack of Treg cells has previously been associated with autoimmune diseases (6). Th17 cells express retinoic acid-related orphan receptor γt and have critical roles in the development of autoimmune diseases and human inflammatory conditions by producing a novel cytokine, interleukin (IL)-17 (7). It has been demonstrated that an imbalance in Th17/Treg cells had an important role in joint inflammation and destruction in an animal model (8). A previous study demonstrated that the imbalance between Th17 and Treg cells is an important mechanism which may lead to RA (2).
Artesunate is a low toxicity and highly efficient immune inhibitor (9). It has previously been demonstrated that artesunate is able to suppress lipopolysaccharide-induced secretion of tumor necrosis factor (TNF)-α by synovial cells by regulating nuclear factor-κB signaling pathways (10,11), thereby inhibiting the synovial inflammation associated with RA. In addition, artesunate inhibited the secretion of IL-17, TNF-α and other inflammatory factors by synovial cells in previous studies (12,13); thus reducing the formation of pannus and erosion of cartilage and bone. However, the effect of artesunate on the balance of Th17/Treg cells in patients with RA remains unknown.
The present study established a rat model of type II collagen-induced arthritis (CIA) in order to investigate the effect of artesunate on the Th17/Treg cell imbalance in vivo and to elucidate the underlying mechanisms.
Materials and methods
Experimental animals
A total of 70 male Sprague Dawley rats (weight, ~100 g; age, 4 weeks) were obtained from the Guilin Medical College Experimental Animal Center (Guilin, China). The rats were maintained at 22–26°C and 55±10% humidity, under a 12-h light/dark cycle with ad libitum access to food and water. The present study was approved by the Ethics Committee of Guilin Medical University (Guilin, China).
Reagents
Collagen type II (5 ml/bottle) was purchased from Chondrex, Inc., (Redmond, WA, USA); Complete Freund's adjuvant (CFA; 10 ml/bottle) was obtained from Sigma-Aldrich (St. Louis, MO, USA); artesunate was purchased from Guilin Pharmaceutical Co., Ltd., (Guilin, China); Leukocyte Activation Cocktail with BD GolgiPlug™ and Lysing Buffer were purchased from BD Pharmingen (San Diego, CA, USA); phycoerythrin (PE)-conjugated anti-rat IL-17A, PE-conjugated anti-rat Foxp3, allophycocyanin (APC)-conjugated anti-rat CD4, PE-conjugated rat IgG2a Isotype Control and the Foxp3/Transcription Factor Staining Buffer Set were obtained from eBioscience, Inc., (San Diego, CA, USA); anti-IL-17 and anti-Foxp3 antibodies were purchased from Abcam (Cambridge, UK).
Establishment of a CIA murine model
Collagen type II (with acetic acid, 2 mg/ml) was slowly added to an equal volume of CFA to a final concentration of 1 mg/ml and maintained on ice until further use. Subsequently, rats were anesthetized with pentobarbital sodium (0.1 ml/100 g; Sigma-Aldrich) and divided into the normal control (n=9) and the CIA model (n=8) groups. The CIA model group was administered a mixed emulsion (0.2 ml) of collagen and adjuvant (1 mg/ml acetic acid) by intradermal injection in the rat tail, and the normal control group was administered an equal volume of saline. Primary immunization was performed on day 0 with 200 mg (0.2 ml), followed by a second immunization on day 7 with 100 mg (0.1 ml). Rats that scored >6 points in the arthritis index (AI) scoring system (14) were used for subsequent analyses.
Treatment with artesunate
CIA rats were divided into four sub-groups, as follows: i) CIA model plus 2 ml saline; ii) CIA model plus 5 mg/kg/day artesunate; iii) CIA model plus 10 mg/kg/day artesunate; and iv) CIA model plus 20 mg/kg/day artesunate. Daily artesunate gavage was initiated on day 14 following primary immunization. All rats were sacrificed in week 20 by cervical dislocation following intraperitoneal injection with 10% chloral hydrate (OriGene Technologies, Inc., Beijing, China). The normal control group was administered an equal volume of physiological saline.
Evaluation of clinical features
Clinical features of the rats were analyzed once a week following primary immunization. This included an assessment of the general health of the rats, including their weight, fur color, feeding behaviour and AI. In addition, the drainage method was used to assess the degree of swelling of the hind legs, as described previously (15).
Degree of joint swelling
A vernier caliper was used to measure the radius of the left leg ankle (from the medial malleolus to the external ankle) and the diameter from the foot heel to the middle point of joint clearance, in order to assess the general incidence degree of joint swelling and the effect of treatment by analyzing the anteroposterior and transverse diameters.
AI
The AI of each rat was calculated prior to primary immunization, following primary immunization, once every 3 days in the acute phase during the initial 6 weeks and once every week in the chronic phase, according to a previous study (16). Briefly, each claw was assigned 4 points, thus the maximum possible score for each rat was 16 points. However, as pathological changes predominantly occurred in the hind legs of rats in the present study, a score of 6–8 points was deemed to indicate severe arthritis.
Molybdenum target X-ray
Joint damage in the left posterior ankle was observed by molybdenum target X-ray mammography at 10 and 21 weeks following primary immunization of the normal control, CIA model and CIA model plus artesunate (20 mg/kg/day) groups. The stage of arthritis was subsequently determined according to the American Rheumatism Association criteria for the classification of rheumatoid arthritis (17), as follows: Normal (0), osteoporosis period (+), bone destruction period (++), bone serious destruction period (+++) and ankylosis period (++++).
Histopathological analysis
Rats were sacrificed at week 20 and the left anklebone was harvested, fixed with 10% neutral formalin for 24 h, decalcified using 10% EDTA, cut vertically, embedded in paraffin and cut into 2-µm slices. Subsequently, the slices were stained with hematoxylin and eosin in order to observe inflammation in the joint under a light microscope, according to a previous study (18). The slices were observed for infiltration of inflammatory cells, including neutrophils, lymphocytes and plasma cells, synovial cell hyperplasia, proliferation of fibrous tissue and erosion of bone and cartilage.
Immunohistochemical analysis
Sections were dewaxed and incubated with citric acid in a pressure cooker for antigen retrieval. After this, the sections were incubated with 0.3% H2O2 for 3 min, washed three times for 3 min each with phosphate-buffered saline (PBS) and incubated with PE-conjugated anti-IL-17A and anti-Foxp3 antibodies for 1 h at 37°C. Subsequently, the sections were washed three times for 3 min each with PBS, followed by incubation with the secondary antibody for 1 h at room temperature. Antibody complexes were visualized with 3,3′-diaminobenzidine, after which the sections were stained with hematoxylin, dehydrated and mounted with gum, prior to visualization under a fluorescent microscope.
Extraction of spleen lymphocytes
Following sacrifice, the rats were soaked in 75% ethanol for 10 min and the spleen was harvested under sterile conditions. Subsequently, the spleen was cut into small pieces using ophthalmic scissors, homogenized and filtered using a 200-mesh steel sieve with the core of a 5 ml syringe to remove large pieces of tissue. The homogenate was centrifuged at 400 × g for 5 min at 4°C, the supernatant was discarded and 5 ml Lysing Buffer was added to the pellet. Spleen cells were subsequently washed 1–2 times with PBS, after which 106 cells/ml underwent flow cytometry in four tubes.
Flow cytometry
Leukocyte Activation Cocktail, with BD GolgiPlug™ (0.5 µl) was added to each tube and incubated at 37°C in 5% CO2 for 6 h. Subsequently, 1 ml fluorescence-activated cell sorting (FACS) buffer (50 ml 10X PBS, 20 g bovine serum albumin, 0.02% NaN3, distilled water) was added to each tube, followed by centrifugation at 400 × g for 5 min at 4°C. The supernatant was discarded and the pellet was resuspended in 100 µl FACS buffer, followed by the addition of 5 µl APC-conjugated CD4 and centrifugation at 350 × g for 5 min at 4°C. In order to rupture the cell membranes, 1 ml Foxp3/permeabilization buffer (BD Pharmingen) was added to each tube and the tubes were incubated at 4°C for 40 min in the dark. Subsequently, 2 ml permeabilization buffer (1X) was added to each tube and the tubes were centrifuged at 350 × g for 5 min at 4°C. The resulting pellet was resuspended in 100 µl permeabilization buffer (1X), followed by the addition of 5 or 10 µl PE-conjugated rat IgG2a isotype control, 5 µl PE-conjugated anti-Foxp3 or 10 µl PE-conjugated anti-IL-17 at 4°C for 30 min in the dark. The tubes were analyzed on a flow cytometer using BD FACSDiva™ Software 6.0 (BD Pharmingen).
Statistical analysis
SPSS 17.0 software (SPSS, Inc., Chicago, IL, USA) was used to conduct statistical analyses. Data were presented as the mean ± standard deviation. One-way analysis of variance was performed to analyze differences among groups. Dunnett's T3 test was used to compare non-parametric data. P<0.05 was considered to indicate a statistically significant difference.
Results
Clinical features of CIA rats
Of the 61 rats in the CIA model group, 56 exhibited arthritic symptoms in 9–21 days following primary immunization (success rate, ~93.3%). Arthritis appeared at 9 days following the primary immunization as redness and swelling in the small toe, foot or ankle. As demonstrated in Fig. 1, AI peaked at ~42 days following immunization in the CIA model group, which was followed by a chronic arthritis phase. At 70 days post-primary immunization, the mean AI was 9 points for the 5 mg/kg/day artesunate group, 7 points for the 10 mg/kg/day artesunate group, 5 points for the 20 mg/kg/day artesunate group, and 10.5 points for the CIA group. At 142 days post-primary immunization, the mean AI was 7 points for the 5 mg/kg/day artesunate group, 5 points for the 10 mg/kg/day artesunate group, 3 points for the 20 mg/kg/day artesunate group and 11.1 points for the CIA group. These results suggest that 20 mg/kg/day artesunate is able to improve joint symptoms in a rat model of RA.
Figure 1.
Arthritis indices of the rat models of type II collagen-induced arthritis. *P<0.05 vs. CIA.
Histopathological analysis of rat ankle joints
As compared with the normal control rats, the levels of synovial fluid in the CIA rats were increased, the joint cavity was disorganized, and infiltration of inflammatory cells, in particular lymphocytes and monocytes, and synovial pannus invasion of joint cartilage and bone, were observed at 10 weeks following primary immunization (Figs. 2A and B). At 21 weeks following the primary immunization, the levels of synovial fluid were increased, the joint cavity was disordered, and infiltration of inflammatory cells and cartilage and bone damage were observed in the CIA rats (Fig. 2C). These results suggested that the rat model of CIA had been established successfully.
Figure 2.
Pathological sections of ankle joints and molybdenum target X-rays of rat limb joints. Pathological sections of ankle joints from (A) a normal rat, (B) a CIA rat at 10 weeks post-primary immunization and (C) a CIA rat at 21 weeks post-primary immunization (magnification, ×400). Molybdenum target X-rays of the rat limb joints from (D) a normal control group rat at 10 weeks post-primary immunization, (E) a CIA rat at 10 weeks post-primary immunization, (F) an artesunate-treated (20 mg/kg/day) rat at 10 weeks post-primary immunization, (G) a normal control group rat at 21 weeks post-primary immunization, (H) a CIA rat at 21 weeks post-primary immunization and (I) an artesunate-treated (20 mg/kg/day) rat at 21 weeks post-primary immunization. CIA, collagen-induced arthritis.
Molybdenum target X-rays of rat limb joints
The structure of the joint cavity was integrated in normal rats. Conversely, CIA rats exhibited signs of osteoporosis, bone and articular cartilage destruction and narrowed joint spaces at weeks 10 and 21 following primary immunization. Rats in the 20 mg/kg/day artesunate group exhibited signs of osteoporosis; however, bone destruction was mild (Fig. 2). These results suggest that artesunate is able to attenuate the bone destruction associated with RA.
Expression of Foxp3 and Il-17 in the synovium
Immunohistochemical analysis demonstrated that Foxp3 was dispersed in the synovial lining cell layer, surrounding blood vessels and cartilage surface, and IL-17 was predominantly located in the synovial lining cell layer and surrounding blood vessels. Expression levels of Foxp3 were markedly increased in the 20 mg/kg/day artesunate group, as compared with the other drug intervention groups and CIA group; however, no marked difference was observed between the 20 mg/kg/day artesunate group and the normal control group. The expression levels of IL-17 were markedly reduced in the 20 mg/kg/day artesunate group, as compared with the CIA group and the other drug intervention groups (Fig. 3).
Figure 3.
Expression of Foxp3/IL-17 in the synovium, as determined by immunohistochemial staining (magnification, ×400). Foxp3 expression in the (A) normal control, (B) collagen-induced arthritis model, (C) 5 mg/kg/day artesunate, (D) 10 mg/kg/day artesunate and (E) 20 mg/kg/day artesunate groups. IL-17 expression in the (F) normal control, (G) CIA model, (H) 5 mg/kg/day artesunate, (I) 10 mg/kg/day artesunate and (J) 20 mg/kg/day artesunate groups. Foxp3, forkhead/winged helix transcription factor; IL-17, interleukin-17.
Expression of Foxp3 in spleen T lymphocytes, as detected by flow cytometry
Foxp3 expression is an indicator of Treg cells. As compared with the normal control group, the expression levels of Foxp3 were significantly decreased in the CIA model group, as compared with the normal control group (P<0.05). The expression levels of Foxp3 were significantly increased in the 20 mg/kg/day artesunate group, as compared with the 10 mg/kg/day artesunate and 5 mg/kg/day artesunate groups (P<0.05; Table I and Fig. 4).
Table I.
Expression of Foxp3/IL-17 in CD4+ T lymphocytes.
| Group | Foxp3 (%) | IL-17 (%) |
|---|---|---|
| Normal | 1.171±0.191a | 0.514±0.352 |
| CIA model | 0.529±0.138a,b | 1.471±0.180a,b |
| Artesunate (mg/kg/day) | ||
| 5 | 0.729±0.095a | 1.257±0.134a,b |
| 10 | 1.342±0.217a,b | 0.829±0.040a,b |
| 20 | 1.671±0.123b | 0.600±0.038 |
P<0.01 vs. the 20 mg/kg/day artesunate group
P<0.01 vs. the normal group. Foxp3, forkhead/winged helix transcription factor; IL, interleukin; CIA, collagen-induced arthritis.
Figure 4.
Expression of Foxp3 in CD4+ T lymphocytes. Spleen cells were incubated with APC-conjugated anti-CD4 and PE-conjugated anti-Foxp3 antibodies and analyzed by flow cytometry. (A) Foxp3 isotype control; (B) normal control group; (C) collagen-induced arthritis model group; (D) 5 mg/kg/day artesunate group; (E) 10 mg/kg/day artesunate group; (F) 20 mg/kg/day artesunate group. Foxp3, forkhead/winged helix transcription factor; APC, allophycocyanin; PE, phycoerythrin.
Expression of IL-17 in spleen T lymphocytes, as detected by flow cytometry
IL-17 expression is an indicator of Th17 cells. As compared with the normal control group, the expression levels of IL-17 were significantly increased in the CIA model group (P<0.05). The expression levels of IL-17 were significantly decreased in the 20 mg/kg/day artesunate group, as compared with the 10 mg/kg/day artesunate and 5 mg/kg/day artesunate groups (P<0.05; Table I and Fig. 5).
Figure 5.
Expression of IL-17 in CD4+ T lymphocytes. Spleen cells were incubated with APC-conjugated anti-CD4 and PE-conjugated anti-IL-17 antibodies and analyzed by flow cytometry. (A) IL-17 isotype control; (B) normal control group; (C) collagen-induced arthritis model group; (D) 5 mg/kg/day artesunate group; (E) 10 mg/kg/day artesunate group; (F) 20 mg/kg/day artesunate group. IL-17, interleukin-17; APC, allophycocyanin; PE, phycoerythrin.
Discussion
RA is a systemic autoimmune disease characterized by peripheral arthritis. At present, the CIA model is the most commonly used animal model for studying RA (19). The underlying etiology and pathogenesis of RA has yet to be fully elucidated, although the expression and balance of Th17/Treg lymphocytes has emerged as a hot research topic in autoimmune diseases. Niu et al (2) reported that Th17 cells were significantly increased, whereas Treg cells were significantly decreased, in the peripheral blood of patients with RA, as compared with healthy controls; thus suggesting that an imbalance of Th17/Treg lymphocytes may underlie the pathogenesis of RA. This is consistent with the present study, which demonstrated that the expression levels of Foxp3 were decreased, and those of Il-17 were increased, in spleen lymphocytes derived from CIA rats.
Artemisinin and its derivatives are the most effective and safe therapeutic agents for the treatment of malignant and chloroquine-resistant malaria (20). In addition, it has been suggested that artemisinin and its derivatives may also exert anti-inflammatory and immunomodulatory effects (21). Artesunate is a semi-synthetic derivative of artemisinin. In our previous study, it was demonstrated that artesunate was able to regulate the NF-κB signaling pathway to inhibit LPS-induced secretion of TNF-α by RA synovial cells, and it was able to lower the activity of IL-17 (13). One aim of the present study was to investigate whether artesunate reduces the activity of IL-17 via increasing the expression of Foxp3, thereby exerting immunomodulatory effects.
The present study demonstrated that intervention with artesunate resulted in an increase in the number of Foxp3-positive T-cells and a decrease in the number of IL-17-positive T cells in a dose-dependent manner. These results suggested that artesunate was able to correct the imbalance of Th17/Treg cells in CIA rats. Traditional treatment of RA involves administration of hydroxychloroquine and methotrexate (22).
The greatest effects were observed with 20 mg/kg/day artesunate. The results of the present study suggested that artesunate was able to control and alleviate the symptoms of CIA rats. A previous study suggested that the effects of artesunate may involve the inhibition of IL-17, TNF-α, MMP3 and other inflammatory factors (23), and the present study demonstrated that these immunomodulatory effects may occur via the induction of Foxp3 expression.
In conclusion, the present study demonstrated that artesunate was able to increase the expression of Foxp3 and decrease the expression of IL-17 in CD4+ T lymphocytes, thereby reversing the imbalance of Th17/Treg cells associated with arthritis. Our investigations of artesunate have identified potential therapeutic targets of artesunate and have highlighted a potential mechanism underlying the intervention of artesunate in human synovial cells. However, further studies to elucidate the potential adverse reactions of artesunate are required prior to the widespread clinical use of artesunate for the treatment of RA.
Acknowledgements
The present study was supported by grants from the Chinese National Natural Science Foundation (grant nos. 81160376 and 81360462), the Guangxi Natural Science Foundation (grant nos. 2013GXNSFAA019111 and 2013GXNSFBA019181), the Guangxi Department of Education Natural Science Foundation (grant no. 201106LX363) and the Guilin Natural Science Foundation (grant no. 20120121-1-7)
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