OP0193 Synovial Fluid Neutrophils Undergoing Netosis Contribute to Joint Inflammation by Producing Citrullinated Autoantigens
Background Anti-citrullinated protein antibodies (ACPA) are characteristically detected in patients with rheumatoid arthritis (RA) and growing evidence suggests that they are involved in disease pathogenesis. During disease flares large numbers of neutrophils enter the joint space of RA patients. Th...
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Veröffentlicht in: | Annals of the rheumatic diseases 2013-06, Vol.72 (Suppl 3), p.A118-A118 |
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Sprache: | eng |
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Zusammenfassung: | Background Anti-citrullinated protein antibodies (ACPA) are characteristically detected in patients with rheumatoid arthritis (RA) and growing evidence suggests that they are involved in disease pathogenesis. During disease flares large numbers of neutrophils enter the joint space of RA patients. These cells can extrude genomic DNA in an active process termed NETosis. NETosis critically depends on histone citrullination by peptidyl deiminase 4 (PAD4). Objectives Here we tested the hypothesis that activation and release of PAD4 during NETosis contributes to the production of autoantigens in the inflamed joint. Methods Levels of extracellular DNA in the synovial fluid (SF) of patients with RA (n=23) and osteoarthritis (OA) (n=15) or crystal arthritis (n=6) were quantified using the non cell-permeable DNA dye SYTOX Green. PAD4, neutrophil elastase, citrullinated proteins and bound human IgG were labelled in association with DNA on smear preparations of RA SF and detected by immunofluorescence. NETs from SF and in vitro stimulated neutrophils were isolated and western blotting and mass spectrometry were used to identify proteins released during NET formation and proteins co-fractionated with NETs. PAD enzymatic activity was determined after NETosis in vitro and in the SF of patients with RA (n=9) and OA (n=9). Results Extracellular DNA was detected in SF from patients with RA and crystal arthritis at significantly higher levels than in OA SF (RA vs. OA p |
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ISSN: | 0003-4967 1468-2060 |
DOI: | 10.1136/annrheumdis-2013-eular.398 |