Candida albicansinduces cyclo-oxygenase 2 expression and prostaglandin E2 production in synovial fibroblasts through an extracellular-regulated kinase 1/2 dependent pathway
© Lee et al.; licensee BioMed Central Ltd. 2009
Received: 19 September 2008
Accepted: 29 March 2009
Published: 29 March 2009
Synovial cells are potential sources of inflammatory mediators in bacterial-induced arthritis but their involvement in the inflammatory response to Candida albicans-induced septic arthritis is largely unknown.
Primary cultures of rat synovial fibroblasts were infected with C. albicans (ATCC90028). Immunocytochemistry, western blotting, and RT-PCR were performed to assess cyclo-oxygenase 2 induction. Phosphorylation of extracellular-regulated kinase (ERK1/2) following infection in the absence or presence of U0126 was assessed by western blotting whilst prostaglandin E2 production was measured by ELISA. Nuclear factor κB (NFκB) translocation was evaluated by an electrophoretic mobility shift assay.
Infection of synovial fibroblasts with C. albicans resulted in cyclo-oxygenase 2 expression and prostaglandin E2 production. Cyclo-oxygenase 2 expression and prostaglandin E2 production was dependent upon extracellular-regulated kinase 1/2 phosphorylation, associated with activation of NFκB and significantly elevated in the presence of laminarin, an inhibitor of dectin-1 activity. Synovial fibroblasts adjacent to C. albicans hyphae aggregates appeared to be the major contributors to the increased levels of cyclo-oxygenase 2 and phosphorylated extracellular-regulated kinase 1/2.
C. albicans infection of synovial fibroblasts in vitro results in upregulation of cyclo-oxygenase 2 and prostaglandin E2 by mechanisms that may involve activation of extracellular-regulated kinase 1/2 and are associated with NFκB activation.
Infectious arthritis is a potentially serious disease that may cause rapid destruction of the joint and produce permanent deformities. Articular structures can be affected by mycotic infections through direct inoculation, contiguous spread, or hematogenous dissemination [1–4]. Of the various Candida species, Candida albicans is most commonly associated with fungal arthritis, especially in immunocompromized individuals [4–7]. Typically infection predominates in large weight-bearing joints, most often the knee . Experimental arthritis in Sprague-Dawley rats with intravenous administration of C. albicans demonstrates that Candida arthritis involves not only joint tissues but also adjacent bones . In mice, direct inoculation of joints with C. albicans results in a rapidly progressive septic arthritis that also exacerbates collagen-induced arthritis . Fungal infection may also induce and exacerbate autoimmune diseases such as rheumatoid arthritis potentially through effects of β-glucans, polysaccharides in the cell wall of fungi, on inflammatory and immune responses .
Cyclo-oxygenase 2 (COX-2) is a key enzyme involved in joint inflammation through production of prostaglandins. COX-2 is induced in human joint tissues, including chondrocytes and synoviocytes, by inflammatory stimuli such as interleukin 1β (IL1β), IL17, and tumor necrosis factor (TNF) [12–20] and has roles in cartilage degradation and synovial angiogenesis [16, 21]. Micro-oganisms of all types, mostly bacterial infections, can produce an infectious arthritis associated with COX-2 induction and prostaglandin E2 (PGE2) production [22–24]. In response to C. albicans infection HeLa cells , vascular endothelial cells , and macrophages in vitro  have been shown to express COX-2. The signal transduction pathways resulting in COX-2 expression may involve Toll-like receptor (TLR) 2 and 4 [25, 28], which activate a variety of signaling molecules including p38 , c-Jun N-terminal kinase (JNK) [29, 30], extracellular-regulated kinase (ERK) [31, 32], protein kinase C (PKC), and activated nuclear factor κB (NFκB) [25, 30]. More recently dectin-1 the receptor for β-glucan a fungal wall component has been shown to be involved in the induction of cytokines and chemokines possibly by collaborating with TLRs .
Although it is well documented that C. albicans may induce joint inflammation and destruction, the detailed inflammatory responses and associated mechanisms are largely unknown. The present study was undertaken to establish a model to examine COX-2 induction in synovial fibroblasts following C. albicans infection in vitro.
Materials and methods
Synovial fibroblast isolation and culture
Male Sprague-Dawley (SD) rats (8 weeks old, 280 to 300 g) were obtained from BioLASCO Taiwan (Taipei, Taiwan). All experiments were approved by the local Institutional Review Board and performed in adherence to the National Institutes of Health Guidelines for the treatment of laboratory animals. The synovium of knee joints was aseptically removed from normal SD rats, cut into small fragments and incubated with antimicrobial solution (500 IU/ml penicillin/streptomycin; Gibco Invitrogen, Burlington, Ontario, Canada) for 1 h, washed with sterile phosphate-buffered saline (PBS) before digestion with 3 mg/ml collagenase type H (Sigma, St Louis, MO, USA) at 37°C for 12 h. The resultant cell suspension was centrifuged at 2,500 rpm for 10 minutes following which the supernatant was discarded and the pellet resuspended in PBS. After further centrifugation at 1,000 rpm for 10 minutes, cells were resuspended and seeded in 20 ml of Ham's F12 medium (Sigma) containing 10% fetal bovine serum (Gibco Invitrogen) and 100 IU/ml penicillin/streptomycin (Gibco Invitrogen). The synovial cells were then cultured in a humidified 5% CO2 atmosphere at 37°C until confluent, detached with 0.05% trypsin/ethylenediaminetetraacetic acid (EDTA) (Gibco Invitrogen) and seeded at a density of 2 × 105 cells/dish in 60 mm tissue culture dishes (Orange scientific, Braine-l'Alleud, Belgium) for further experimental procedures.
C. albicans (ATCC 90028) was grown on Sabouraud dextrose agar (BD Microbiology System, Sparks, MD, USA) at 25°C. After a 16-h culture, colonies were suspended in PBS (Gibco Invitrogen) and prepared to the desired density of 1 × 103 to 1 × 107 yeasts/ml.
Experimental protocol for C. albicansincubation with synovial fibroblasts
Dishes of synovial fibroblasts were placed in serum-free media (3 ml) overnight and then treated with either 200 μL PBS or 200 μL suspension of C. albicans (2 × 102 to 2 × 106 yeasts/dish) in 5% CO2 atmosphere at 37°C for 6 or 12 h. In some experiments synovial fibroblasts were pre-incubated with U0126 (Cell Signaling Technology, Beverly, MA, USA), a mitogen-activated protein kinase (MEK)1/2 inhibitor, at a concentration of 20 μM for 2 h; laminarin (Sigma) a β-glucan receptor blocking agent and specific inhibitor of dectin-1 activity at a concentration of 10 mg/ml for 1 h. MG-132 (Calbiochem, San Diego, CA, USA) as a NFκB inhibitor was co-incubated with synovial fibroblasts at a concentration of 35 μM. For the trans-well experiments (Transwell, Corning Incorporated, Corning, NY, USA), synovial fibroblasts were seeded in the upper chamber and C. albicans were plated in the lower chamber overnight, and then interacted for 12 h. In controls C. albicans were omitted from the lower chamber.
After a 12-h co-culture of synovial fibroblasts and C. albicans, cells and fungi on dish were washed with ice-cold PBS twice and then fixed using 2 ml of a 1:1 methanol/acetone mixture per dish for 5 minutes at -20°C. Cells were then stained by immunocytochemistry. Immunodetection for COX-2 was performed with a standard avidin-biotin-peroxidase complex detection kit (DakoCytomation, Glostrup, Denmark). Dishes were washed twice with PBS and blocked by incubation with 200 μL 1% non-immune horse serum (Vector Laboratories, Burlingame, CA, USA) in 1% bovine serum albumin (BSA) in antibody diluent (DakoCytomation) for 30 minutes at room temperature. The solution was poured off and the cells incubated sequentially with anti-COX-2 epitope specific antibody (1:200) (Lab Vision Corporation, Cheshire, UK) or anti-phospho-ERK1/2 (1:100) (Cell Signaling) for 60 minutes, biotinylated secondary antibody (1:200) for 45 minutes, and horseradish peroxidase (HRP)-conjugated streptavidin for 20 minutes. Between each incubation cells were washed with Tris-buffered saline/Tween (TBST) (12.5 mM Tris/HCl, pH 7.6, 137 mM NaCl, 0.1% Tween 20) three times. The chromogen 3-amino-9-ethylcarbazole (AEC) was then added for 15 minutes and finally counterstained with Mayer's hematoxylin. The cells were mounted with a coverslip and visualized under light microscopy.
Reverse transcription PCR
Total RNA was isolated from cells after a 12-h co-culture of synovial fibroblasts and C. albicans using easy-BLUE Total RNA Extraction Kit (iNtRON Biotechnology, Gyeonggi-do, Korea). For first strand cDNA synthesis, 3 μg of total RNA was used in a single-round RT reaction (total volume 20 μl), containing 0.75 μg oligo(dT)14 primer, 1 mM deoxynucleosides (dNTPs), 1 × first strand buffer, 0.4 mM dithiothreitol (DTT), 40 units RNaseOut recombinant ribonuclease inhibitor, and 200 units of superscript II reverse transcriptase (Gibco Invitrogen). The reverse transcription reaction was performed at 42°C for 2 h, followed by 95°C for 5 minutes. PCR was run using 0.9 μl of the reverse transcription reaction mixture as template, 0.4 mM of gene specific primers, 1 × PCR buffer, 0.25 mM dNTPs, and 1.5 units of Taq DNA polymerase (BioMan, Taipei, Taiwan). The amplification was carried out at 94°C for 1 minute, then for 30 cycles at 94°C for 1 minute, 56°C for 1 minute, and 72°C for 1 minute followed by a final extension at 72°C for 10 minutes. All PCR products were size-fractionated by a 1.5% agarose gel electrophoresis, and DNA bands were visualized by staining the gel with 0.1 μg/ml ethidium bromide. The bands were analyzed using gel documentation system (Bio-Profil, Bio-1D version 99; Viogene, Sunnyvale, CA, USA). The values were expressed as ratio of the band intensity of the target gene to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the ratio of the band intensity of COX-2/GAPDH in the control condition was normalized to 1. Variance and P values were analyzed by Alphaimager 1220 V5.5 (Alpha Innotech Corporation, San Leandro, CA, USA). A Student t test was used for statistical comparison between groups. A P value of less than 0.05 was considered statistically significant.
The primers used were as follows: COX-2 5'-GTCTCTCATCTGCAATAATGTG-3' (sense) and 5'-ATCTGTGTGGGTACAAATTTG-3' (antisense) ([GenBank:S67722]; PCR product 801 base pairs (bp)); GAPDH 5'-CCCATCACCATCTTCCAGGAG-3' (sense) and 5'-GTTGTCATGGATGACCTTGGCC-3' (antisense) ([GenBank:X02231]; PCR product 284 bp).
Analysis of COX-2, ERK1/2 and phospho-ERK1/2 expression
Following C. albicans infection cells for 12 h were immediately washed with ice-cold PBS containing 100 μM Na3VO4 (Sigma) and lysed in situ with ice-cold lysis buffer at 4°C for 15 minutes. Lysis buffer contained 1% Igepal (Sigma), 100 μM Na3VO4, and a protease inhibitor cocktail tablet (Roche Diagnostics, Mannheim, Germany). Whole cell lysates were collected after centrifugation at 14,500 rpm for 15 minutes. Protein concentration was determined by the Lowry method. Equal amounts of protein (20 μg) were loaded onto 10% SDS polyacrylamide gels and were transferred to polyvinylidene difluoride (PVDF) membranes (Millipore Immobilon-P, Sigma). Membranes were blocked overnight at 4°C with 2% BSA in TBST. After washing three times with TBST, blots were incubated for 1 h at room temperature with primary antibody (anti-COX-2, 1/1,000 dilution; anti-total ERK1/2, 1/2,000 dilution; anti-phospho-ERK1/2, 1/2,000 dilution) diluted with 2% BSA in TBST. After washing six times with TBST, the blots were then incubated with HRP-labeled secondary antibody (1/1,000 dilution) for 1 h at room temperature. Membranes were rewashed extensively and binding was detected using Enhanced Chemiluminescense western blotting detection system (Amersham Pharmacia Biotech, Piscataway, NJ, USA), according to the manufacturer's instructions. Anti-ERK1/2 and phospho-ERK1/2 antibodies were from Cell Signaling Technology. Mouse monoclonal antibody tubulin Ab-4 (primary antibody, 1/5,000 dilution; secondary antibody, 1/20,000 dilution) (Lab Vision) served as internal control. The band was semiquantified by densitometry using systems as described above.
Activation of NFκB by electrophoretic-mobility shift assay (EMSA)
Cells were infected with 2 × 105 C. albicans at 37°C for 6 h. Nuclear and cytoplasmic extracts of synovial fibroblasts were prepared using NE-PER nuclear and cytoplasmic extraction reagents according to the manufacturer's protocols (Pierce, Rockford, IL, USA). A non-radioactive EMSA was performed using an EMSA kit according to the manufacturer's instructions (Panomics, Redwood City, CA, USA). Nuclear protein (8 μg) was used to bind biotinylated oligonucleotides containing the NFκB binding site for 30 minutes at room temperature. The blank control was nuclear extracts being replaced with water. A competition/cold control was set up by adding non-biotin-labeled cold probes to the reaction. Samples were separated in a non-denaturing polyacrylamide gel (6%, with 2.5% glycerol) and blotted on a Biodyne B Pre-cut Modified Nylon membrane (Pierce). The biotin was labeled with alkaline phosphatase-conjugated streptavidin and alkaline phosphatase was detected with Enhanced Chemiluminescense western blotting detection system (Amersham). The band was semiquantified by densitometry using systems as described above.
Measurement of PGE2, IL1β, and TNFα production in culture medium
Cells were infected with 2 × 105 C. albicans in the presence or absence of U0126 (20 μM, pre-incubation for 2 h) at 37°C for 12 h. The culture supernatant was harvested, and PGE2, IL1β, and TNFα concentrations were measured by ELISA (R&D Systems, Minneapolis, MN, USA) according to the manufacturer's instructions.
COX-2 induction by C. albicansinfection
To ascertain whether COX-2 induction was mediated by production of a soluble mediator in the system culture medium was collected from co-cultures of synovial fibroblasts and C. albicans and added directly to non-infected synovial fibroblasts. No change in COX-2 expression was seen. The levels of IL1β and TNFα production were also undetectable (data not shown).
ERK1/2 activation is necessary for C. albicansinduction of COX-2 expression
Laminarin effect and trans-well experiment
The present study has demonstrated that synovial fibroblast expression of COX-2, under the control of ERK1/2, is induced following C. albicans infection. Upregulation of COX-2 is associated with NFκB activation and appears to be more prominent in synovial fibroblasts adjacent to fungal colonies.
The finding that ERK1/2 phosphorylation occurs on exposure of synovial fibroblasts to C. albicans is consistent with observations of interactions of C. albicans with inflammatory and epithelial cells. Phagocytosis of C. albicans by macrophages results in ERK phosphorylation  and TNFα production by monocytes exposed to C. albicans is ERK dependent . TLR2 appears to be the major receptor mediating PGE2 production by mouse macrophages in response to C. albicans . C. albicans increases COX-2 expression in HeLa cells with roles for both TLR2 and TLR4 being identified . Similar mechanisms are likely to be involved in the induction of COX-2 and PGE2 production in the current study.
Toll-like receptors have been shown to be involved in synovial inflammation in a wide range of inflammatory joint diseases including rheumatoid arthritis [34, 35], Lyme arthritis , and streptococcal cell wall-induced arthritis . TLR signaling is also likely to be involved in mediating proinflammatory responses and subsequent tissue destruction in fungal arthritis. The basic cell wall structure of C. albicans consists of a linear β-glucan backbone from which there are covalently attached branches of additional β-glucan and mannoproteins. Mannoproteins, highly antigenic proteins with large numbers of mannose groups attached have been shown to induce pro-inflammatory cytokine production in murine macrophages and human mononuclear cells . Mannose-containing molecular patterns are also strong inducers of COX-2 expression and PGE2 production in human macrophages . TLR have important roles in the induction of cytokines by fungi with TLR4 recognition of O-linked mannosyl residues present in the C. albicans cell wall are thought to be particularly important. Phospholipomannan, present in the cell surface of C. albicans, has been shown to be recognized by TLR2 . Cytokine induction by C. albicans may also be through recognition of β-glucan by the dectin-1 (dentritic cell-associated C-type lectin-1)/TLR2 receptor complex .
Dectin-1, a major β-glucan receptor, has a number of antimicrobial functions in phagocytes including induction of cytokines and chemokines, possibly by collaborating with TLRs, involvement in endocytosis and phagocytosis and production of the respiratory burst . Rat dectin-1 is involved in immune responses against fungi . Laminarin, a soluble form of glucan blocks signaling through dectin-1 . Laminarin decreases TNFα production by macrophages in response to zymosan and C. albicans infection . In the current study laminarin partially blocked the increase in COX-2 mRNA that is seen when synovial fibroblasts are infected with C. albicans. This indicates that signaling through dectin-1 has a partial role in the upregulation of COX-2 gene expression. This may be through direct contact between C. albicans and synovial fibroblasts as the elevation of COX-2 gene expression was similar in trans-well experiments and experiments with laminarin where contact between C. albicans and synovial fibroblasts was possible.
We show for the first time that COX-2 induction and PGE2 production occurs following infection of C. albicans to synovial fibroblasts and that this requires ERK1/2 activation and is associated with NFκB activation. These interactions may significantly contribute to the detrimental inflammatory/catabolic activities of synovial fibroblasts in septic arthritis induced by C. albicans and other fungi.
bovine serum albumin
enzyme-linked immunosorbent assay
electrophoretic-mobility shift assay
c-Jun N-terminal kinase
mitogen-activated protein kinase
nuclear factor κB
protein kinase C
reverse transcription polymerase chain reaction
tumor necrosis factor.
This study was supported by a grant from the National Science Council and National Defense Medical Center, Tri-Service General Hospital, Taiwan (NSC95-2320-B-016-018-MY2, NSC97-2320-B-016-009-MY3, DOD96-13-03 and DOD97-08-06).
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