NALP3 was widely expressed in the lining and sub-lining areas (Fig. 1a). Double labelling studies were performed and showed that NALP3 was expressed by a proportion of CD31+ endothelial cells, CD68+ cells, CD20+ B cells and almost all MPO-positive neutrophils, but was not found in CD3+ T cells (Fig. 1b). As for ASC, it was also abundantly detected (Fig. 2a) in T and B cells, macrophages, neutrophils and endothelial cells

(Fig. 2b). Taken together, these results indicate that in RA and OA synovial tissue, many different cell types express NALP3 and ASC, but T cells did not express NALP3. The expression of messenger RNAs (mRNAs) encoding the different NLRs, ASC as well as caspase-1, caspase-5 was examined by reverse transcription–polymerase chain selleck chemicals reaction (RT-PCR). NALP1, NALP3, NALP6, NALP10, NALP12 and NALP14 were readily detected in both RA and OA synovium (Table 1), whereas no expression

selleck compound of NALP5 and NALP13 was found in any of the samples analysed. Expression of the other NALPs (2, 4, 7, 8, 9, 11) was not ubiquitous, and was positive in a proportion of the samples analysed. Both caspase-1 and caspase-5 were expressed. Western blots confirmed the protein expression of ASC and NALP1, NALP3 and NALP12 in the synovium. (Fig. 1). In macrophages and keratinocytes, IL-1β processing is dependent on the inflammasome. As fibroblasts comprise a major resident cell population in the synovium, they may play a part in the production of inflammatory cytokines from the results described above. We first assessed the presence of the molecular components of the inflammasome by RT-PCR. The FLS from RA patients (n = 3) were cultured in the presence or absence of crude LPS, a known activator of the NALP3 inflammasome. We found expression of NALPs 1, 2, 3, 8, 10, 12 and 14 as well as of ASC, caspase-1

and caspase-5 in both unstimulated and LPS-stimulated cells (Fig. 3a). Under the same conditions, NALPs 4, 5, 6, 9, 11 and 13 were not detected and a variable expression of NALP7 Glutamate dehydrogenase and NALP8 was observed. Expression of ASC was confirmed by Western blot of unstimulated and LPS-stimulated FLS (Fig. 3b) as well as by immunohistochemistry (Fig. 3c). Although NALP3 mRNA was readily detectable in FLS, no NALP3 protein could be demonstrated by Western blot or immunohistochemistry (Fig. 3b,c). We investigated if FLS could process and secrete IL-1β when activated by stimuli that are known to induce IL-1β secretion in macrophages. Interleukin-1β levels were measured in cell lysates and in supernatants. Intracellular levels of IL-1β increased in response to the different stimuli, except for ATP and H2O2 (Table 2). However, this was not paralleled by secretion of IL-1β into the culture supernatant, as no IL-1β was detected by ELISA (detection limit 2 pg/ml) or by Western blotting (results not shown). Similarly, intracellular levels of caspase-1 were elevated when FLS were stimulated, but secreted caspase-1 was not detected in the supernatants.