Elevated levels of fibrinogen-derived endogenous citrullinated peptides in synovial fluid of rheumatoid arthritis patients
© Raijmakers et al.; licensee BioMed Central Ltd. 2012
Received: 30 January 2012
Accepted: 14 May 2012
Published: 14 May 2012
Rheumatoid arthritis (RA) is an autoimmune disease characterized by inflammation of the joints and the presence of autoantibodies directed against proteins containing the non-standard arginine-derived amino acid citrulline. The protein fibrinogen, which has an essential role in blood clotting, is one of the most prominent citrullinated autoantigens in RA, particularly because it can be found in the inflamed tissue of affected joints. Here, we set out to analyze the presence of citrullinated endogenous peptides in the synovial fluid of RA and arthritic control patients.
Endogenous peptides were isolated from the synovial fluid of RA patients and controls by filtration and solid phase extraction. The peptides were identified and quantified using high-resolution liquid chromatography-mass spectrometry.
Our data reveal that the synovial fluid of RA patients contains soluble endogenous peptides, derived from fibrinogen, containing significant amounts of citrulline residues and, in some cases, also phosphorylated serine. Several citrullinated peptides are found to be more abundantly present in the synovial fluid of RA patients compared to patients suffering from other inflammatory diseases affecting the joints.
The increased presence of citrullinated peptides in RA patients points toward a possible specific role of these peptides in the immune response at the basis of the recognition of citrullinated peptides and proteins by RA patient autoantibodies.
Rheumatoid arthritis (RA) is one of the most common autoimmune diseases, for which many autoantigens have been identified over the last decades. The most remarkable but yet most common targets of autoantibodies in RA are proteins containing the amino acid citrulline. This group of proteins includes, among others, histones and fibrin(ogen) [1–3]. Autoantibodies against citrullinated proteins (ACPA) are almost exclusively present in RA and can be present years before disease onset . Detection of ACPA or other autoantibodies is a common part of the clinical diagnosis of RA. ACPA are often detected using the so-called cyclic citrullinated peptide, or CCP test .
Fibrinogen is a heteromultimeric protein consisting of two copies each of three different peptide chains (alpha, beta and gamma) . It plays an essential role in the clotting cascade, where it is proteolytically cleaved by thrombin to form the clotting protein fibrin . Citrullinated forms of the alpha and beta chains of fibrinogen are known to be present in the serum and synovial fluid (SF) of RA patients and can be targets for ACPA [1, 8]. The role of citrullinated proteins and antibodies recognizing these proteins in the pathophysiology of RA is not fully understood, but specific human leukocyte antigen (HLA) alleles (HLA-DR4 and HLA-DR1, HLA-DR10 and HLA-DR14) have been linked to a predisposition to develop RA and the associated major histocompatibility complex (MHC) molecules were found to show increased ability to present peptides containing a citrulline residue [9, 10]. Importantly, HLA-DR4 transgenic mice are susceptible to develop arthritis when immunized with citrullinated fibrinogen . Recently, Ho and others found that mice that were immunized with citrullinated fibrinogen developed arthritis and fibrinogen-reactive T cells which produce the proinflammatory cytokines IL-6, IL-17, TNF-alpha, and IFN-gamma and that these mice possess rheumatoid factor (RF), circulating immune complexes and anti-CCP antibodies, all of which are characteristics of human RA . Inhibition of the enzymes responsible for the generation of citrulline residues in proteins, the peptidylarginine deiminases (PADs), has been shown to reduce symptoms in mouse models of RA . Immune complexes consisting of ACPA and citrullinated fibrinogen can also be found in a large part of the ACPA-positive RA patients  and are known to induce macrophage secretion of TNF-alpha, an important mediator of inflammation in RA .
Although the presence of citrullinated fibrinogen protein has attracted the most attention lately, it is known that fibrinogen-derived peptides can be present in the synovial fluid of inflamed joints  and that (citrullinated) peptides can be potent activators of cells of the immune system [8, 16]. Here, we analyzed the synovial fluid obtained from 11 RA patients and 10 patients with related inflammatory diseases of the joint for the presence of endogenous soluble citrullinated peptides by liquid chromatography-tandem mass spectrometry (LC-MS/MS). We found that fibrinogen-derived citrullinated peptides were significantly more abundant in the fluid of the RA patients compared to the control patients, while their noncitrullinated counterparts were present at similar levels.
Materials and methods
Synovial fluid samples
Synovial fluid samples were obtained from 11 RA patients and 10 patients with other inflammatory diseases (four with psoriatic arthritis, two with ankylosing spondylitis, two with gout, one with osteoarthritis and one with ochronosis). Synovial fluid was obtained by joint punctures (arthrocentesis), using needles with a diameter from 1.6 to 2.2 mm. A sample was immediately centrifuged at 2,500 × g for 10 minutes at 4°C. Supernatant and pellet were separately stored at -80°C. All procedures were performed within two hours. All samples were collected for diagnostic purposes and all patients gave informed consent that the samples could also be used anonymously for research purposes, in accordance with the ethical guidelines as established by the ethics committee of the University Medical Centre Ljubljana (Slovenia).
Isolation of peptides from synovial fluid
Peptides were isolated from synovial fluid based on the protocol recently described by Kamphorst et al. . First, intact proteins were removed from the synovial fluid by ultracentrifugation. Spin filter columns with a 10 kD cutoff were first washed with 100 μl ethanol by centrifugation for 10 minutes at 11,000 × g at 4°C and then with 100 μl 50 mM NH4HCO3 pH 7, also for 10 minutes at 11,000 × g at 4°C. Next, 50 μl of synovial fluid was mixed with 235 ul of 50 mM NH4HCO3 pH 7 and 15 μl DMSO and was passed through the spin filter by centrifugation for 60 minutes at 11,000 × g at 4°C. The spin filter was then washed again with 100 μl 50 mM NH4HCO3 pH 7 for 10 minutes at 11,000 × g at 4°C and the filtrates of the last two steps were combined and acidified with 5 μL formic acid (FA). Next, Sep-Pak C18 (Waters Corp., Milford, MA, USA) disposable cartridges with a capacity of 50 mg were activated with 1 ml acetonitrile (ACN) and conditioned with 1 ml 2.5% ACN/1% FA. After passing the filtrates over the cartridges, they were washed with 1 ml 2.5% ACN/1% FA. Finally, peptides were eluted with 150 μL 80% ACN/1% FA and dried by vacuum centrifugation. For mass spectrometry (MS) analysis, dried peptide samples were reconstituted in 50 μl of 5% FA. Five μl of each sample was spiked with 1 μl of internal standard, containing three standard peptides with mass-to-charge ratio (m/z) of 556.28, 477.78, and 497.60.
Identification and quantitation of endogenous peptides by LC-MS/MS
Isolated synovial fluid peptides were analyzed by nanoscale liquid C18 chromatography using an Agilent 1100 series LC system coupled to an LTQ-FT-ICR mass spectrometer (Thermo Fisher Scientific Inc., Waltham, MA, USA). The mass spectrometer was operated in the data-dependent mode to automatically switch between MS and MS/MS acquisition and the five most intense ions were fragmented in the linear ion trap using collisionally induced dissociation.
Obtained MS/MS spectra were analyzed by database searching against all human proteins in the SwissProt database using the Mascot software platform version 2.1.0 (Matrix Science Ltd., London, UK). The search criteria included methionine oxidation, arginine citrullination and asparagine and glutamine deamidation as variable modifications. The peptide tolerance was set to 5 ppm and the MS/MS tolerance to 0.6 Da. All searches were done without enzyme restrictions and peptides were, unless described differently, identified with a minimum Mascot score of 35. For spectral counting, peptide spectrum matches with a Mascot score of at least 20 were included. Technical details of the LC-MS/MS analysis and database searching can be found in Additional file 1.
To assess the presence of citrullinated endogenous peptides in the synovial fluid of RA patients, synovial fluid and serum was collected from 11 RA patients and 10 patients with other inflammatory diseases of the joint. The ACPA (anti-citrullinated protein antibody) status of all RA patients was assessed by ELISA using the CCP2 test and is given in Additional file 1, Table S1. Endogenous peptides with a size smaller than 10 kDa were isolated from the synovial fluid by ultrafiltration and solid phase extraction.
Identification of endogenous citrullinated peptides
List of citrullinated peptides identified more often in rheumatoid arthritis patients compared to control patients.
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Fibrinogen α chain
Peroxisome proliferator-activated receptor gamma coactivator-related protein 1
Plasma membrane calcium-transporting ATPase 3
Quantification of endogenous citrullinated peptides
Synovial fluid contains multiply modified fibrinopeptide A
Interestingly, fibrinopeptide A also contains a known phosphorylation site on fibrinogen alpha (S22) , which is most likely generated by a member of the casein kinase II (CK2) family . To determine if the presence or absence of phosphorylation was in any way linked to the citrullination of R35, we extended our database search to include this possibility and were able to identify two peptides (with sequences ADpSGEGDFLAEGGGVcR and DpSGEGDFLAEGGGVcR) containing both a phosphorylated S22 and a citrullinated R35 in a number of the patients (Additional file 1, Figure S3A). We then also determined the XIC areas of these peptides in all patients, showing that the peptides containing both modifications showed a similar behavior to the peptides containing only the citrullination site (for example, more present in RA patients), whereas peptides containing only the phosphorylation site were equally abundant in all patients (Additional file 1, Figure S3B). A final fibrinopeptide A-derived phosphopeptide containing a citrulline residue with sequence pSGEGDFLAEGGGVcR was identified with low identification scores in some of the samples, but was found to be present in only very low amounts and was, therefore, not included in this analysis (data not shown).
Many citrullinated proteins have been identified in the inflamed joints of RA patients and a number of these have been shown react in vitro with ACPA. A prominent candidate to be the main target for ACPA is fibrin(ogen), which is known to be present in large amounts in inflamed joints and which is known to be present in a citrullinated form in the synovial fluid of RA patients [3, 21]. ACPA can indeed bind to citrullinated fibrinogen, in particular the alpha chain. Recently, it was shown that in inflamed joints also significant amounts of peptides can be found that are derived from fibrinogen, due to endogenous proteolytic activity . Here, we showed that citrullinated versions of these peptides can be found in the synovial fluid of inflamed joints. While some of these citrullinated peptides were equally abundant in the RA patients and the control group with patients suffering from other inflammatory joint diseases, others appeared to be more abundant in RA patients (Table 1). Consistent with that observation, PAD activity in joints is known to be elevated in such other inflammatory diseases as well. The higher level of some of the peptides in RA patients suggests that a different immune response toward these peptides might occur in RA patients, leading to, for example, prolonged retention of these peptides, which, in turn, could contribute to increased immune system activation. Although there was significant diversity in the levels of citrullinated peptides in the control group, with especially patient S2 (ankylosing spondylitis) showing very high levels, no obvious relation with their diagnosed disease was apparent (Additional file 1, Table S1). This diversity among the patients in the control group confirms that the citrullinated peptides arose from inflammatory events that can also occur in diseases other than RA, which is not unexpected as many rheumatic diseases show overlap in the symptoms observed. An ideal control material would be synovial fluid from healthy individuals, but for obvious reasons this material is less readily available, not only due to ethical issues, but also because the amount of synovial fluid in noninflamed joints is much smaller.
The citrullinated peptides we found to be most abundantly present in RA patients covered mainly two distinct regions in the alpha chain of fibrinogen, amino acids 20-35 and 414-433. These regions have been shown to be susceptible to citrullination in the past and it was shown that the arginine residues in these sequences (R35, R425 and R426) can be citrullinated by both the PAD2 as well as the PAD4 enzymes , both known to be present in inflammatory cells in the synovium . Together, these PAD enzymes are known to be able to citrullinate two-thirds of all arginine residues in fibrinogen , but little is known about which citrullinated residues contribute most to eliciting the anti-citrullinated protein immune response. The fact that specific citrullinated fibrinogen-derived peptides reside in the synovial fluid makes them prime candidates for having a role in the immune response against citrullinated epitopes.
The fibrinogen region between amino acids 414-433 is known to be autoantigenic in RA patients [6, 22], but for the citrullinated fibrinopeptide A (amino acids 20-35) no data on autoantigenicity is available, most likely because it is not part of the mature fibrinogen protein that has been used in such studies most frequently.
Interestingly, the fact that fibrinopeptide A, after cleavage from the fibrinogen precursor, contains a C-terminal arginine residue makes it an excellent substrate for PAD enzymes, which are able to efficiently convert such residues to citrulline (data not shown).
Both sequence elements were represented by a variety of peptides, differing in either their N- or C-terminal sequence (Figures 4 and S1), most likely due to in vivo proteolytic activities. While it is difficult to predict the enzyme responsible for their generation, proteases abundantly present in inflammatory cells, such as matrix metalloproteinases, elastases or caspases are likely involved. The two cleavage sites generating the full amino acids 20-35 fragment, however, are obvious, as this corresponds exactly to the borders of fibrinopeptide A, which is released from the A-alpha chain by cleavage at the N-terminal side of amino acid 20 by the signal peptidase and at the C-terminal side of amino acid 35 by thrombin [7, 24] The latter cleavage is one of the first steps of the clotting cascade and therefore the presence of (derivatives of) fibrinopeptide A is not very surprising, although its presence in a citrullinated fashion has not been reported before. Because thrombin cleavage at that position is dependent on the presence of an arginine residue, the citrullination of the C-terminal arginine of fibrinopeptide A has most likely occurred after thrombin cleavage. Citrullination of R35 in the uncleaved fibrinogen protein would inhibit thrombin cleavage and might, therefore, have implications on the efficiency of clotting in inflamed joints . The cleavage generating the N-terminus of the amino acids 414-433 fragment is most likely mediated by cathepsin D, which can cleave fibrinogen at that position in the process of clearing fibrin cloths .
Fibrinogen is certainly not the only citrullinated antigen present in synovial fluid as, for example, citrullinated fibronectin and vimentin have also been found . However, the presence of high levels of endogenous citrullinated peptides derived from the protein is quite unique to fibrinogen, and could potentially provide a direct link between with the generation of an immune response targeting citrullinated epitopes. From a diagnostic point of view, such peptides might be very interesting to discriminate RA from closely related inflammatory diseases that also affect the joints. This could be achieved either by employing targeted mass spectrometric techniques or by the development of alternative, for example, antibody-based methods that would allow the specific detection of these citrullinated peptides in synovial fluid samples.
We have shown the presence of increased amounts of specific endogenous citrullinated peptides, derived from fibrinogen, in the synovial fluid of RA patients. Citrullinated fibrinopeptide A was found to be present more abundantly in RA patients compared to control patients and compared to the not citrullinated fibrinopeptide. This elevated presence could indicate a role for such endogenously generated, citrullinated peptides in the development of the anti-citrullinated protein antibody (ACPA) immune response that is often seen in RA patients.
anti-citrullinated protein antibodies
cyclic citrullinated peptide
enzyme-linked immunosorbent assay
human leukocyte antigen
liquid chromatography-tandem mass spectrometry
major histocompatibility complex
tumor necrosis factor
extracted ion chromatogram.
This work was supported in part by the Dutch Technology Foundation (STW) and the Netherlands Proteomics Centre (NPC). We are thankful to the clinicians of the Department of Rheumatology of the UMC Ljubljana (Slovenia) for patient samples and clinical data.
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