Heavy metal exposure reverses genetic resistance to Chlamydia-induced arthritis
© Inman and Chiu; licensee BioMed Central Ltd. 2009
Received: 9 August 2008
Accepted: 9 February 2009
Published: 9 February 2009
We have previously observed that Brown Norway (BN) rats display a relative resistance to experimental Chlamydia-induced arthritis. In the present study, we examine an environmental toxin, mercuric chloride (HgCl2), as a modulator of this innate resistance to arthritis.
To assess the effect of the heavy metal exposure, one group of rats received two subcutaneous injections of HgCl2 (1 mg/kg) 48 hours apart. Seven days later, the animals received the intra-articular injection of synoviocyte-packaged Chlamydia.
Histopathology revealed that BN rats receiving only Chlamydia had a minimal cellular infiltration in the joint, which was predominantly mononuclear in character. In contrast, mercury-exposed rats had a marked exacerbation of the histopathological severity of the arthritis, and the infiltration was predominantly neutrophilic. Mercury exposure was also associated with marked enhancement in IgE levels and an alteration in IgG2a/IgG1 ratio, reflecting a Th2 shift. The local cytokine profile in the joint was markedly altered after mercury exposure, with a suppression of tumour necrosis factor-alpha and interferon-gamma but an enhancement of vascular endothelial growth factor. This was associated with decreased host clearance capacity reflected in enhanced bacterial load in both the spleen and the joint and was accompanied by enhanced detection of microbial antigens in the synovial tissues by immunohistological staining.
Genetically defined cytokine production in the joint defines the severity of reactive arthritis by dictating the local clearance of the pathogen. This interplay can be altered dramatically by heavy metal exposure, which results in suppression of protective cytokines in the microenvironment of the joint.
Many rheumatic diseases are thought to reflect an interplay of genetic susceptibility and environmental triggers, but there are few examples in which strong clues for the nature of these interacting elements are known. One such example is reactive arthritis (ReA), in which susceptible individuals develop an aseptic arthritis following an extra-articular infection. Yet dissecting the immune mechanisms in ReA has proven to be difficult in the clinical setting. Experimental Chlamydia trachomatis-induced arthritis (CtIA) affords the opportunity to systematically address the factors that define outcomes after exposure to this arthritogenic pathogen . We have recently observed that the Brown Norway (BN) rat is resistant to CtIA , with minimal transient inflammation in the joint. The infiltrating cell population in the joint is primarily mononuclear in nature and joint damage is minimal. This contrasts with an aggressive neutrophilic infiltration with associated joint injury that is seen in susceptible strains.
In contrast to their inherent resistance to this arthritis, BN rats are uniquely susceptible to the development of a variety of autoimmune conditions mediated mainly through Th2 mechanisms . One such condition is the development of autoimmunity subsequent to an exposure of mercury . The hallmarks of this condition are the increase of circulating IgE, the overproduction of interleukin-4 (IL-4), and the activation of Th2 cells [5, 6]. The normal CD4/CD8 balance and their associated cytokines are markedly disrupted . This is accompanied by the appearance of a range of autoantibodies [5, 8, 9]. Early pivotal studies examining the effects of mercuric chloride (HgCl2) in rats documented a significant increase in total IgE and this was observed in BN rats but not in Lewis rats . Subsequent studies revealed that HgCl2 induction of IL-4 was accompanied by a decrease in CD23 expression on B cells and that IL-2, IL-6, and IL-10 were upregulated as well as IL-4 following HgCl2 exposure in BN rats [11, 12]. Because the BN rat displays a dichotomy of resistance to infection-triggered arthritis but susceptibility to mercury-induced immune disruption, we addressed how these factors would interact if they were temporally related in the rat.
Materials and methods
Eight week-old male BN rats were purchased from Harlan Laboratories, Inc. (Indianapolis, IN, USA). The animals were maintained in microisolators under specific pathogen-free conditions in the animal care facility of the Toronto Western Hospital. All animals studied were less than 12 weeks of age. The studies were conducted with the approval of the Animal Care Committee of the University Health Network.
Induction of arthritis
Chlamydia trachomatis-induced arthritis
Arthritis was induced in the rats by intra-articular injection of synoviocyte-packaged Chlamydia as described . Briefly, C. trachomatis serotype L2 was inoculated onto monolayers of rat synovial fibroblasts (SFs) in tissue culture. These stable SF lines were developed as described . After overnight incubation, cells were harvested and adjusted to 5 × 10 PP5PP/mL. Rats were anaesthetized with isoflurane (Pharmaceutical Partners of Canada, Richmond Hill, ON, Canada), and 0.2 mL of the infected cells containing 2 × 10 PP5PP colony-forming units (CFU) of Chlamydia was injected into the knee joint. Joint swelling was measured with a caliper and recorded in millimetres. Animals were euthanized at day 7 post-injection. Mock injections on non-infected synoviocytes had previously been shown to induce only a transient inflammation in the joint.
Protocol and injection schedule for HgCl2
Several different dose schedules have been used previously by investigators to address response to HgCl2 [5, 6, 8, 9]. Roos and colleagues [13, 14] used a two-injection abbreviated schedule to investigate the short-term effects of HgCl2 exposure. This protocol was associated with less morbidity than other protocols using five injections over a 10-day period. These investigators observed that distinctive immunological changes were rapid and were observed as early as 4 days after the initial HgCl2 exposure, with minimal toxicity. We therefore adopted the two-injection protocol of Roos and colleagues [13, 14]. HgCl2 (Sigma-Aldrich, St. Louis, MO, USA) was dissolved in water at 1 mg/mL and then filter-sterilized. The rats were anaesthetized by inhalation using isoflurane, weighed, and injected with the HgCl2 solution subcutaneously at a dosage of 1 mg/kg of body weight. Two days later, the injection procedure was repeated. The animals tolerated this procedure well, with no local or systemic adverse effects noted. There was no joint swelling or joint discomfort noted following the two injections of HgCl2. Seven days after the second HgCl2 injection, the rats were anaesthetized again and synoviocyte-packaged Chlamydia (2 × 105 CFU) was delivered by intra-articular injection into the knee joint in accordance with our established protocol . Control rats without antecedent exposure to HgCl2 received a similar intra-articular injection of synviocyte-packaged Chlamydia. One week after the injection of the joint, the animals were sacrificed by anaesthetic overdose. Eight animals were used for each comparative experimental condition.
Processing and pathology
The knee joints were removed and fixed in formalin. The lateral width of each joint was measured with a caliper. After measurement, the joints were decalcified and processed for histopathological scoring as described . Immunopathology studies used a primary antibody specific for C. trachomatis (AbD Serotec, Oxford, Oxfordshire, UK) that was developed with a peroxidase-conjugated anti-mouse antibody.
The Dako IDEIA™ PCE Chlamydia Kit (Dako, Ely, Cambridgeshire, UK) was used for determining the clearance of the pathogen. Seven days after the intra-articular injection of Chlamydia, the HgCl2-exposed and non-exposed rats were sacrificed. Spleens were removed and ground over a Falcon Cell Strainer (BD Biosciences 2280 Argentia Road, Mississauga, ON L5N 6H8, Canada) using the rubber end of a syringe in a Petri dish containing 10 mL of phosphate-buffered saline (PBS). The tissue homogenate suspensions were frozen at -70°C until tested. For analysis of synovial tissue, the injected joints were dissected and the tissues were removed. Tissues were stored in 1 mL of the transport buffer provided with the enzyme-linked immunosorbent assay (ELISA) kit and then were frozen as above.
Blood was obtained from the rats at sacrifice by cardiac puncture. Sera were separated and frozen at -70°C until used. Results reflect serological changes 14 days after HgCl2 exposure and 7 days after onset of CtIA.
Total serum IgE
Elevation in serum IgE is the hallmark of Hg-induced autoimmunity in the BN rat. The ELISA for total serum IgE was performed using an antibody pair kit from AbD Serotec in accordance with the protocol of the manufacturer. A mouse anti-rat IgE monoclonal antibody was used to coat the ELISA plate. All sera were diluted 1:100 and incubated in the wells for 90 minutes. This was followed by the second antibody, peroxidase-conjugated anti-rat kappa/lambda, which was used at a 1:2,000 dilution for a second 90-minute incubation. O-phenylenediamine (Sigma-Aldrich) was used for development, and the plates were read at 490 nm.
The anti-Chlamydia antibody ELISA followed our published methods . ELISA plates were coated with a 10-μg/mL preparation of Chlamydia in a pH 9.6 carbonate-bicarbonate buffer overnight at 4°C. A single batch of plates was prepared and kept frozen. Rat sera were diluted 1:200 in PBS containing 1% bovine serum albumin (BSA) as blocking agent, and 0.2 mL was added to each well in triplicate. After 90 minutes of incubation at 37°C, plates were washed and peroxidase-conjugated antibodies were added. Peroxidase-conjugated goat anti-rat IgG1 and IgG2a secondary antibodies were obtained from Bethyl Laboratories, Inc. (Montgomery, TX, USA) and used at a 1:10,000 dilution. After a further 90-minute incubation at 37°C, the plates were washed and colour-developed with o-phenylenediamine (0.4 mg/mL) as substrate. Plates were read at 490 nm with an ELISA plate reader.
The ELISA kit for the rat anti-type II collagen antibodies was from Chondrex (Redmond, WA, USA) and followed the protocol of the manufacturer. Rat serum was run at a 1:200 dilution in the assay.
Serum and synovial tissue cytokine levels in the Hg-exposed and non-exposed BN rats were assayed as previously described . Rat interferon-gamma (IFN-γ), tumour necrosis factor-alpha (TNF-α), IL-4, and IL-10 were assayed by ELISA kits purchased from Pierce Endogen (Thermo Fisher Scientific Inc., Rockford, IL, USA). The ELISA for rat vascular endothelial growth factor (VEGF) was purchased from Bender MedSystems (Vienna, Austria).
The kit to determine total nitric oxide (NO) concentrations was from R&D Systems (Minneapolis, MN, USA) (KGE001). This is a colorimetric assay using the Griess reaction with the entire procedure performed on an ELISA plate. The serum samples are filtered through 10,000-molecular weight cutoff spin filter units (Millipore Microcon YM-10; Millipore Corporation, Billerica, MA, USA) prior to the assay. Serum samples (0.5 mL in size) were loaded on top of the filter units and then centrifuged in Eppendorf centrifuge at a speed of 14,000 rotations per minute for 30 minutes at room temperature.
The Student t test was used to compare statistical differences between groups.
Acute inflammatory response
The HgCl2-exposed BN rats (n = 8) had higher levels of IgG antibodies to rat type II collagen than did controls: 0.108 ± 0.069 versus 0.032 ± 0.012 (P < 0.01). These serological changes paralleled the enhanced severity of arthritis clinically and histologically following HgCl2 exposure (Figure 4b).
Nitric oxide and vascular endothelial growth factor
The spondyloarthropathies (SpAs) refer to a group of diseases that share several common features: association with HLA class I genes, asymmetric oligoarthritis, axial involvement, enthesitis, and characteristic extra-articular features such as uveitis. The role of infection as a triggering factor is implicated with varying degrees of certainty amongst the SpA subcategories, with ReA having the most clear evidence for a microbial trigger . The most direct causal evidence for microbial triggers for ReA derives from a demonstration of microbial antigens in the joint . The case for intra-articular pathogens is strongest for Chlamydia, and several investigators have used polymerase chain reaction to demonstrate Chlamydia DNA or RNA in the joints of patients with post-Chlamydia ReA [17–19]. There is some evidence that these organisms are metabolically altered and may have entered a quiescent phase [20, 21]. Several studies support the notion of a viable organism present, at least transiently, in the early stages of ReA. It is speculated that this may reflect defective killing of the organism by failure either to internalize the pathogen or to effectively initiate intracellular killing. There has been particular interest in the Chlamydia heat shock proteins, notably heat shock protein 60 (hsp60), and recent studies have identified differential expression of three C. trachomatis hsp60-encoding genes that may differ in active versus persistent infections . The cellular response to Chlamydia infection has been studied by microarray techniques, and 18 genes appeared to be selectively upregulated following infection with C. trachomatis . Profiling Chlamydia infection of U937 monocytic cells  and human lung epithelial cells  has provided a profile of induced gene expression and, in particular, which cytokines are induced by this microbial challenge.
Analysis of cytokine profiles is a further method for studying the link between infection and ReA. In a study of 11 patients with ReA, it was observed that stimulation of SF mononuclear cells resulted in secretion of low amounts of IFN-γ and TNF-α but high amounts of IL-10 . IL-10 was responsible for suppression of IFN-γ and TNF-α as judged by the effect of adding IL-10 or anti-IL-10 to the cells. The suppression of Th1-like cytokines is likely mediated through suppression of IL-12 synthesis. This IL-10/IL-12 balance, resulting in a predominance of Th2 cytokines, may contribute to the persistence of bacteria in the joint. In comparison with rheumatoid arthritis, SF levels of TNF-α in ReA are lower despite comparable levels of IL-2 receptor, again implicating a relative deficiency of protective antimicrobial cytokines in the local environment . Analysis of synovial fluid cytokines has been studied in patients with Chlamydia-induced arthritis and it was found that B27+ patients had lower SF IFN-γ levels and it was these patients who had a more chronic course . This suggests that diminished IFN-γ generation might account for the persistence of the arthritis.
Our previous studies in experimental ReA have paralleled these clinical findings. BN rats that are relatively resistant to CtIA exhibit an enhanced IFN-γ and TNF-α expression in the microenvironment of the joint. This is accompanied by enhanced clearance of the pathogen and a more transient and benign course of the arthritis. In the present study, we have found that this inherent resistance to ReA can be overcome by heavy metal exposure. Mercury exposure alters the cytokine profile, host clearance capability, and histopathological outcome from the resistant phenotype to the susceptible phenotype. Our findings contrast with the experience studying murine collagen-induced arthritis, in which prior exposure to HgCl2 did not influence the outcome of the arthritis, but exposure following the onset did have an aggravating effect on the arthritis .
If HgCl2 diminishes protective cytokines in the microenvironment of the joint, what is driving the aggressive inflammation and subsequent joint damage? Our study suggests that NO and VEGF are two important candidates. We have previously studied NO contribution to clearance of arthritogenic pathogens by synoviocytes and observed that in some instances there was an IFN-γ-mediated suppression of NO in such cells, suggesting a dynamic interaction between these two factors . This interaction may be specific to the cells under investigation since, in the case of J774 macrophages, IFN-γ mediated an increase in NO production, which in turn reduced viability of C. pneumoniae in the infected cells . In our in vivo model, the rise in NO was concurrent with an increase in chlamydial load in the host, suggesting that the increase in NO was not sufficient to contain an expanded replication profile of the organism. In this regard, it is interesting to note that, in murine cells, blockage of NO synthesis only partially rescues chlamydial growth, suggesting that there are other important IFN-γ-inducible antichlamydial mechanisms operative .
Prior studies on the effect of Hg on NO have yielded varying results depending on the experimental conditions. Kim and colleagues  found that Hg treatment of a macrophage cell line results in a drop in NO production upon stimulation with lipopolysaccharide. However, Huang and colleagues  discovered that treatment of mice with Hg resulted in an increase in serum NO levels. The latter results are very much in parallel with our finding of an increase of NO following exposure to HgCl2.
The pathological studies in our rats indicate that the exacerbation of histological severity of the arthritis was accompanied by a neovascularization process locally. It is known that VEGF plays a crucial role in angiogenesis. Spondylarthritis is characterized by enthesitis and synovitis, in which new blood vessels participate in perpetuating the inflammation. Serum analysis from SpA patients has documented that VEGF levels were significantly higher in SpA patients than in controls. In SpA patients, serum VEGF levels correlated with disease activity indices as defined by the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), erythrocyte sedimentation rate, or C-reactive protein (CRP). These results suggest that VEGF and therefore angiogenesis may play a role in SpA pathogenesis and may serve as a disease activity marker in SpAs . In keeping with these findings, it has been observed that there is a significant reduction in serum VEGF levels after the infliximab treatment of SpA patients and that these changes correlate with similar reductions in CRP and IL-6 . Direct Chlamydia-endothelial cell interactions are known to mediate induction of VEGF .
Mercury exists in elemental, inorganic, and organic forms. The general population is exposed primarily to mercury vapour from dental amalgam and to organic mercury from fish consumption . Mercury accumulates in the food chain such that large fish such as tuna and swordfish have high concentrations of mercury in tissues . Occupational exposure is primarily to mercury vapour and occurs in dentistry, mining, and the manufacture of electrical equipment. Mercury vapour is well absorbed through the respiratory tract, but absorption of elemental mercury is negligible orally whereas oral absorption of organic mercury is nearly complete . There is recent evidence from studies of human peripheral mononuclear cells that low-dose exposure to mercury can polarize the immune response toward Th2 .
The role of mercury in rheumatic diseases has received little attention. One recent study implicated mercury exposure as a risk factor for Wegener granulomatosis , but the mechanism whereby mercury exposure could alter immune response and set the stage for chronic inflammatory conditions has not been resolved. Our experimental system demonstrates that genetic susceptibility can be fundamentally altered by a heavy metal exposure. This suggests that several environmental factors may act in concert in the pathogenesis of ReA. The immediate precipitating factor may be a bacterial infection, but this occurs in the context of other factors in the environment which influence the immune repertoire. The plasticity of the immune response, even when encoded in its basic elements by heritable factors, is highlighted in this genetic-environment interaction. As significant advances in the genetic basis of rheumatic diseases are being made, it will be a challenge to address the environmental factors with equal rigour.
Genetically defined cytokine production in the joint defines the severity of ReA by dictating the local clearance of the pathogen. This interplay can be dramatically altered by heavy metal exposure, which results in suppression of protective cytokines in the microenvironment of the joint.
Chlamydia trachomatis-induced arthritis
enzyme-linked immunosorbent assay
heat shock protein 60
tumour necrosis factor-alpha
vascular endothelial growth factor.
The source of funding for this article was the Canadian Institutes of Health Research.
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