Matrix metalloproteinase-8 is expressed in rheumatoid synovial fibroblasts and endothelial cells. Regulation by tumor necrosis factor-alpha and doxycycline

• Published in: The Journal of biological chemistry Vol. 272; no. 50; pp. 31504 - 31509
• Main Authors: Hanemaaijer, R, Sorsa, T, Konttinen, Y T, Ding, Y, Sutinen, M, Visser, H, van Hinsbergh, V W, Helaakoski, T, Kainulainen, T, Rönkä, H, Tschesche, H, Salo, T
• Format: Journal Article
• Language: English
• Published: United States 12-12-1997
• Subjects: Arthritis, Rheumatoid - enzymology; Catalysis - drug effects; Cells, Cultured; Collagenases - biosynthesis; Doxycycline - pharmacology; Endothelium - drug effects; Endothelium - enzymology; Endothelium, Vascular - enzymology; Enzyme Inhibitors - pharmacology; Fibroblasts - drug effects; Fibroblasts - enzymology; Glycosylation; Humans; Matrix Metalloproteinase 8; RNA, Messenger - metabolism; Synovial Membrane - cytology; Synovial Membrane - drug effects; Synovial Membrane - enzymology; Tetradecanoylphorbol Acetate - pharmacology; Tumor Necrosis Factor-alpha - pharmacology; Up-Regulation - drug effects
• ISSN: 0021-9258
• DOI: 10.1074/jbc.272.50.31504

Neutrophil collagenase (matrix metalloproteinase-8 or MMP-8) is regarded as being synthesized exclusively by polymorphonuclear neutrophils (PMN). However, in vivo MMP-8 expression was observed in mononuclear fibroblast-like cells in the rheumatoid synovial membrane. In addition, we detected MMP-8 mRNA expression in cultured rheumatoid synovial fibroblasts and human endothelial cells. Up-regulation of MMP-8 was observed after treatment of the cells with either tumor necrosis factor-alpha (10 ng/ml) or phorbol 12-myristate 13-acetate (10 nM). Western analysis showed a similar regulation at the protein level. The size of secreted MMP-8 was 50 kDa, which is about 30 kDa smaller than MMP-8 from PMN. Conditioned media from rheumatoid synovial fibroblasts contained both type I and II collagen degrading activity. However, degradation of type II collagen, but not that of type I collagen, was completely inhibited by 50 microM doxycycline, suggesting specific MMP-8 activity. In addition, doxycycline down-regulated MMP-8 induction, at both the mRNA and protein levels. Thus MMP-8 exerts markedly wider expression in human cells than had been thought previously, implying that PMN are not the only source of cartilage degrading activity at arthritic sites. The inhibition of both MMP-8 activity and synthesis by doxycycline provides an incentive for further studies on the clinical effects of doxycycline in the treatment of rheumatoid arthritis.