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Effects of tumor necrosis factor α and β on resorption of human articular cartilage and production of plasminogen activator by human articular chondrocytes
Author(s) -
Campbell Ian K.,
Piccoli Diana S.,
Roberts Michael J.,
Muirden Kenneth D.,
Hamilton John A.
Publication year - 1990
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.1780330412
Subject(s) - chondrocyte , tumor necrosis factor alpha , cartilage , plasminogen activator , collagenase , cytokine , immunology , chemistry , endocrinology , microbiology and biotechnology , medicine , biology , anatomy , biochemistry , enzyme
Abstract We examined the effects of recombinant human tumor necrosis factor (TNF) on human articular cartilage and chondrocytes in culture. Both TNF α and TNFβ stimulated cartilage matrix breakdown during prolonged culture and elevated the levels of plasminogen activator (PA) activity in both the supernatants and cell layers of cultured chondrocytes. Characterization of the PA activities by immunochemistry and by zymography following gel electrophoresis indicated that human chondrocytes produce both urokinase‐type PA and tissuetype PA in response to TNF. The addition of both interleukin‐1 and TNFα or TNFβ to chondrocyte cultures demonstrated a synergism between these cytokines in the generation of PA activity in the culture supernatants and cell layers. Our results suggest that both activated lymphocytes and monocytes may contribute to the cartilage destruction of inflammatory arthritis through their stimulation of chondrocytes with TNFβ and TNFα, respectively. Since PA is the only neutral proteinase reported to be elevated in TNF‐stimulated chondrocyte cultures, it could have an important role in TNF‐mediated cartilage destruction.

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