THU0114 The Loss of S100A4 Prevents Joint Destruction and Systemic Bone Loss in hTNFtg Mouse Model. (23rd January 2014)

• Record Type: Journal Article
• Authors: Tomcik, M.; Böhm, C.; Scholtysek, C.; Andres Cerezo, L.; Baum, W.; Dees, C.; Beyer, C.; Avouac, J.; Zerr, P.; Palumbo-Zerr, K.; Distler, A.; Becvar, R.; Distler, O.; Grigorian, M.; Krönke, G.; Schett, G.; Distler, J. H.; Senolt, L.
• Is Part Of: Annals of the rheumatic diseases. Volume 72:Supplement 3(2013)
• Page Start: A201
• Page End: A201
• Publication Date: 2014-01-23
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/annrheumdis-2013-eular.642
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Background: Our previous studies demonstrated increased levels of S100A4 protein in sera, synovial fluid and synovial membrane of patients with rheumatoid arthritis (RA) compared to osteoarthritis. S100A4 regulates apoptosis and induces production of matrix metalloproteinases by synovial fibroblasts. Furthermore, S100A4 stimulates synthesis of tumour necrosis factor (TNF)-α by mononuclear cells. Objectives: To investigate the effect of loss of S1004 in induction of experimental arthritis in the human TNF transgenic (hTNFtg) mouse model. Methods: We crossed the heterozygous hTNFtg mice with S100A4 knockout (S100A4-/-) mice. Mice were clinically assessed for paw swelling, grip strength and body weight weekly from week 6 to 14 in a blinded manner. Sections of hind paws and tibias were histologically analyzed for synovial inflammation, cartilage loss, bone erosions, osteoclast numbers and bone formation parameters with the OsteoMeasure image analysis system. Results: In the group of hTNFtg;S100A4-/- mice, paw swelling, grip strength and body weight were significantly improved compared to hTNFtg;S100A4+/+ (p<0.01for all parameters). Consistent with the clinical observations, histological analysis of the tarsal joints of hTNFtg;S100A4-/- mice showed reduced pannus formation (area of inflammation decreased by 66±3%, p<0.01) and cartilage destruction (cartilage loss decreased by 63±6%, p<0.01) compared to hTNFtg;S100A4+/+ mice. Similarly, osteoclast numbers were decreased by 84±3%, (p<0.01) and bone erosions were less severe (area of bone erosion decreased by 81±4%, p<0.01) in hTNFtg;S100A4-/- mice. Furthermore, hTNFtg;S100A4-/- mice were protected from systemic bone loss. Absence of S100A4 completely reversed increased osteoclast formation and bone resorption in hTNFtg mice. hTNFtg; S100A4-/- mice had an increased bone volume per total volume (BV/TV) by 78±20% (p<0.05), a decrease in trabecular separation by 39±4% (p<0.05), decreased numbers of osteoclasts per bone perimeter (N.Oc/B.Pm decreased by 43±2%, p<0.01), decreased bone surface covered by osteoclasts (Oc.S/BS decreased by 52±3%, p<0.01), increased numbers of osteoblasts per bone perimeter (N.Ob/B.Pm increased by 129±20%, p<0.05) and increased bone formation rate per bone surface (BFR/BS increased by 112±18%, p<0.05) compared to hTNFtg;S100A4+/+. Conclusions: These results suggest that inhibition of S100A4 effectively prevents induction of experimental arthritis via protecting against TNF-induced synovial inflammation, cartilage and bone destruction, and systemic bone loss. Our results support the role of S100A4 in the pathogenesis of RA where an increased S100A4 protein in circulation and locally at sites of inflammation may be linked to the process of aggressive fibroblast behaviour. Thus, S100A4 might represent a novel therapeutic target in RA. Acknowledgements: This study was supported by IGA NT 13698-4 grant. Disclosure of Interest: None Declared