Calgizzarin (S100A11): a novel inflammatory mediator associated with disease activity of rheumatoid arthritis
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28446208
PubMed Central
PMC5405489
DOI
10.1186/s13075-017-1288-y
PII: 10.1186/s13075-017-1288-y
Knihovny.cz E-zdroje
- Klíčová slova
- Calgizzarin, Disease activity, Inflammation, Rheumatoid arthritis, S100 proteins,
- MeSH
- biologické markery MeSH
- dospělí MeSH
- kultivované buňky MeSH
- lidé středního věku MeSH
- lidé MeSH
- mediátory zánětu metabolismus MeSH
- progrese nemoci * MeSH
- proteiny S100 metabolismus MeSH
- průřezové studie MeSH
- revmatoidní artritida diagnóza metabolismus MeSH
- senioři MeSH
- synoviální tekutina metabolismus MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
- mediátory zánětu MeSH
- proteiny S100 MeSH
- S100A11 protein, human MeSH Prohlížeč
BACKGROUND: Calgizzarin (S100A11) is a member of the S100 protein family that acts in different tumors by regulating a number of biologic functions. Recent data suggest its association with low-grade inflammation in osteoarthritis (OA). The aim of our study is to compare S100A11 expression in the synovial tissues, synovial fluid and serum of patients with rheumatoid arthritis (RA) and osteoarthritis (OA) and to characterize the potential association between S100A11 and disease activity. METHODS: S100A11 protein expression was detected in synovial tissue from patients with RA (n = 6) and patients with OA (n = 6) by immunohistochemistry and immunofluorescence. Serum and synovial fluid S100A11 levels were measured by ELISA in patients with RA (n = 40) and patients with OA (n = 34). Disease activity scores in 28 joints based on C-reactive protein (DAS28-CRP) were used to assess disease activity. Cytokine content in peripheral blood mononuclear cells (PBMCs), synovial fibroblasts (SFs) and synovial fluid was analysed by ELISA, western blotting or cytometric bead array. RESULTS: S100A11 expression was significantly up-regulated in the synovial lining and sublining layers (p < 0.01) and vessels (p < 0.05) of patients with RA compared to patients with OA, and was associated with fibroblasts and T cells. S100A11 was significantly increased in synovial fluid (p < 0.0001) but not in serum (p = 0.158) from patients with RA compared to patients with OA when adjusted for age and sex. Synovial fluid S100A11 correlated with DAS28 (r = 0.350, p = 0.027), serum CRP (r = 0.463, p = 0.003), synovial fluid leukocyte count (r = 0.677, p < 0.001), anti-cyclic citrullinated peptide antibodies (anti-CCP) (r = 0.424, p = 0.006) and IL-6 (r = 0.578, p = 0.002) and IL-8 (r = 0.740, p < 0.001) in synovial fluid from patients with RA. PBMCs and SFs isolated from patients with RA synthesized and spontaneously secreted higher levels of S100A11 in comparison with PBMCs and SFs from patients with OA (p = 0.011 and 0.03, respectively). S100A11 stimulated the production of the pro-inflammatory cytokine IL-6 by PBMCs (p < 0.05) and SFs (p < 0.01). CONCLUSIONS: Our data provide the first evidence of S100A11 up-regulation and its association with inflammation and disease activity in patients with RA.
1st Orthopaedic Clinic 1st Faculty of Medicine Charles University Prague Czech Republic
Department of Rheumatology 1st Faculty of Medicine Charles University Prague Czech Republic
Institute of Rheumatology Na Slupi 4 12850 Prague Czech Republic
Zobrazit více v PubMed
McInnes IB, Schett G. Cytokines in the pathogenesis of rheumatoid arthritis. Nat Rev Immunol. 2007;7:42942. doi: 10.1038/nri2094. PubMed DOI
Todoroki H, Kobayashi R, Watanabe M, Minami H, Hidaka H. Purification, characterization, and partial sequence analysis of a newly identified EF-hand type 13-kDa Ca(2+)-binding protein from smooth muscle and non-muscle tissues. J Biol Chem. 1991;266:18668–73. PubMed
Seemann J, Weber K, Gerke V. Annex I targets S100C to early endosomes. FEBS Lett. 1997;11(413):185–90. doi: 10.1016/S0014-5793(97)00911-3. PubMed DOI
Mailliard WS, Haigler HT, Schlaepfer DD. Calcium-dependent binding of S100C to the N-terminal domain of annexin I. J Biol Chem. 1996;12(271):719–25. doi: 10.1074/jbc.271.2.719. PubMed DOI
Seemann J, Weber K, Gerke V. Structural requirements for annexin I-S100C complex-formation. Biochem J. 1996;319:123–9. doi: 10.1042/bj3190123. PubMed DOI PMC
Zhao XQ, Naka M, Muneyuki M, Tanaka T. Ca(2+)-dependent inhibition of actin-activated myosin ATPase activity by S100C (S100A11), a novel member of the S100 protein family. Biochem Biophys Res Commun. 2000;267:77–9. doi: 10.1006/bbrc.1999.1918. PubMed DOI
Sakaguchi M, Miyazaki M, Inoue Y, Tsuji T, Kouchi H, Tanaka T, et al. Relationship between contact inhibition and intranuclear S100C of normal human fibroblasts. J Cell Biol. 2000;12(149):1193–206. doi: 10.1083/jcb.149.6.1193. PubMed DOI PMC
Makino E, Sakaguchi M, Iwatsuki K, Huh NH. Introduction of an N-terminal peptide of S100C/A11 into human cells induces apoptotic cell death. J Mol Med (Berl) 2004;82:612–20. doi: 10.1007/s00109-004-0560-1. PubMed DOI
Cecil DL, Johnson K, Rediske J, Lotz M, Schmidt AM, Terkeltaub R. Inflammation-induced chondrocyte hypertrophy is driven by receptor for advanced glycation end products. J Immunol. 2005;175:8296–302. doi: 10.4049/jimmunol.175.12.8296. PubMed DOI
Inada H, Naka M, Tanaka T, Davey GE, Heizmann CW. Human S100A11exhibits differential steady-state RNA levels in various tissues and a distinct subcellular localization. Biochem Biophys Res Commun. 1999;263:135–8. doi: 10.1006/bbrc.1999.1319. PubMed DOI
Sakaguchi M, Sonegawa H, Murata H, Kitazoe M, Futami J, Kataoka K, et al. S100A11, a dual mediator for growth regulation of human keratinocytes. Mol Biol Cell. 2008;19:78–85. doi: 10.1091/mbc.E07-07-0682. PubMed DOI PMC
Cross SS, Hamdy FC, Deloulme JC, Rehman I. Expression of S100 proteins normal human tissues and common cancers using tissue microarrays: S100A6, S100A8, S100A9 and S100A11 are all overexpressed in common cancers. Histopathology. 2005;46:256–69. doi: 10.1111/j.1365-2559.2005.02097.x. PubMed DOI
Broome AM, Eckert RL. Microtubule-dependent redistribution of a cytoplasmic cornified envelope precursor. J Invest Dermatol. 2004;122:29–38. doi: 10.1046/j.0022-202X.2003.22105.x. PubMed DOI
Salama I, Malone PS, Mihaimeed F, Jones JL. A review of the S100 proteins in cancer. Eur J Surg Oncol. 2008;34:357–64. doi: 10.1016/j.ejso.2007.04.009. PubMed DOI
Sakaguchi M, Miyazaki M, Takaishi M, Sakaguchi Y, Makino E, Kataoka N, et al. S100C/A11 is a key mediator of Ca(2+)-induced growth inhibition of human epidermal keratinocytes. J Cell Biol. 2003;163:825–35. doi: 10.1083/jcb.200304017. PubMed DOI PMC
Foertsch F, Teichmann N, Kob R, Hentschel J, Laubscher U, Melle C. S100A11 is involved in the regulation of the stability of cell cycle regulator p21(CIP1/WAF1) in human keratinocyte HaCaT cells. FEBS J. 2013;16:3840–53. doi: 10.1111/febs.12378. PubMed DOI
Amin AR, Islam AB. Genomic analysis and differential expression of HMG and S100A family in human arthritis: upregulated expression of chemokines, IL-8 and nitric oxide by HMGB1. DNA Cell Biol. 2014;33:550–65. doi: 10.1089/dna.2013.2198. PubMed DOI PMC
Cecil DL, Terkeltaub R. Transamidation by transglutaminase 2 transforms S100A11 calgranulin into a procatabolic cytokine for chondrocytes. J Immunol. 2008;180:8378–85. doi: 10.4049/jimmunol.180.12.8378. PubMed DOI PMC
Yu H, Lu C, Tan MT, Moudgil KD. The gene expression profile of preclinical autoimmune arthritis and its modulation by a tolerogenic disease-protective antigenic challenge. Arthritis Res Ther. 2011;13:R143. doi: 10.1186/ar3457. PubMed DOI PMC
Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, et al. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988;31:315–24. doi: 10.1002/art.1780310302. PubMed DOI
Damgaard D, Senolt L, Nielsen CH. Increased levels of peptidylarginine deiminase 2 in synovial fluid from anti-CCP-positive rheumatoid arthritis patients: association with disease activity and inflammatory markers. Rheumatology (Oxford) 2016;55:918–27. doi: 10.1093/rheumatology/kev440. PubMed DOI PMC
Klingelhofer J, Senolt L, Baslund B, Nielsen GH, Skibshøj I, Pavelka K, et al. Up-regulation of metastasis-promoting S100A4 (Mts 1) in rheumatoid arthritis: putative involvement in the pathogenesis of RA. Arthritis Rheum. 2007;56:779–89. doi: 10.1002/art.22398. PubMed DOI
Andrés Cerezo L, Kuklová M, Hulejová H, Vernerová Z, Pešáková V, Pecha O, Veigl D, Haluzík M, Pavelka K, Vencovský J, Senolt L. The level of fatty acid-binding protein 4, a novel adipokine, is increased in rheumatoid arthritis and correlates with serum cholesterol levels. Cytokine. 2013;64:441–7. doi: 10.1016/j.cyto.2013.05.001. PubMed DOI
Foell D, Kane D, Bresnihan B, Vogl T, Nacken W, Sorg C, et al. Expression of the pro-inflammatory protein S100A12 (EN-RAGE) in rheumatoid and psoriatic arthritis. Rheumatology (Oxford) 2003;42:1383–9. doi: 10.1093/rheumatology/keg385. PubMed DOI
Sunahori K, Yamamura M, Yamana J, Takasugi K, Kawashima M, Yamamoto H, et al. The S100A8/A9 heterodimer amplifies proinflammatory cytokine production by macrophages via activation of nuclear factor kappa B and p38 mitogen-activated protein kinase in rheumatoid arthritis. Arthritis Res Ther. 2006;8:R69. doi: 10.1186/ar1939. PubMed DOI PMC
Cerezo LA, Remáková M, Tomčik M, Gay S, Neidhart M, Lukanidin E, et al. The metastasis-associated protein S100A4 promotes the inflammatory response of mononuclear cells via the TLR4 signalling pathway in rheumatoid arthritis. Rheumatology (Oxford) 2014;53:1520–6. doi: 10.1093/rheumatology/keu031. PubMed DOI
Oslejsková L, Grigorian M, Gay S, Neidhart M, Senolt L. The metastasis associated protein S100A4: a potential novel link to inflammation and consequent aggressive behaviour of rheumatoid arthritis synovial fibroblasts. Ann Rheum Dis. 2008;67:1499–504. doi: 10.1136/ard.2007.079905. PubMed DOI
Oslejsková L, Grigorian M, Hulejová H, Vencovsky J, Pavelka K, Klingelhofer J, et al. Metastasis-inducing S100A4 protein is associated with the disease activity of rheumatoid arthritis. Rheumatology (Oxford) 2009;48:1590–4. doi: 10.1093/rheumatology/kep316. PubMed DOI
Andrés Cerezo L, Mann H, Pecha O, Pleštilová L, Pavelka K, Vencovsky J, et al. Decreases in serum levels of S100A8/9 (calprotectin) correlate with improvements in total swollen joint count in patients with recent-onset rheumatoid arthritis. Arthritis Res Ther. 2011;13:R122. doi: 10.1186/ar3426. PubMed DOI PMC
Hammer HB, Odegard S, Fagerhol MK, Landewé R, van der Heijde D, Uhlig T, et al. Calprotectin (a major leucocyte protein) is strongly and independently correlated with joint inflammation and damage in rheumatoid arthritis. Ann Rheum Dis. 2007;66:1093–7. doi: 10.1136/ard.2006.064741. PubMed DOI PMC
Hurnakova J, Zavada J, Hanova P, Hulejova H, Klein M, Mann H, et al. Serum calprotectin (S100A8/9): an independent predictor of ultrasound synovitis in patients with rheumatoid arthritis. Arthritis Res Ther. 2015;17:252. doi: 10.1186/s13075-015-0764-5. PubMed DOI PMC
Erlandsson MC, Forslind K, Andersson SE, Lund A, Bokarewa MI. Metastasin S100A4 is increased in proportion to radiographic damage in patients with RA. Rheumatology (Oxford) 2012;51:932–40. doi: 10.1093/rheumatology/ker362. PubMed DOI
Brentano F, Schorr O, Gay RE, Gay S, Kyburz D. RNA released from necrotic synovial fluid cells activates rheumatoid arthritis synovial fibroblasts via Toll-like receptor 3. Arthritis Rheum. 2005;52:2656–65. doi: 10.1002/art.21273. PubMed DOI
Simard JC, Cesaro A, Chapeton-Montes J, Tardif M, Antoine F, Girard D, Tessier PA. PLoS One. S100A8 and S100A9 induce cytokine expression and regulate the NLRP3 inflammasome via ROS-dependent activation of NF-κB(1.). PLoS One. 2013;8:e72138. PubMed PMC