The production of tissue inhibitor of metalloproteinases (TIMP) in human uterine cervical fibroblasts was increased by human recombinant tumor necrosis factor α (hrTNF) at a low concentration (0.005 81127-A/asset/equation/feb2001457939081127a-math-si1.gif?v=1&s=cfd3e7db48ed6d0788e3466c33a5430d604559d5)
) but the elevated synthesis was suppressed in a dose-dependent manner at higher concentrations (up to 50 81127-A/asset/equation/feb2001457939081127a-math-si2.gif?v=1&s=b2eaf0842cc78cee10e28a598f89a020cf380c51)
). In contrast, the production of collagenase (EC 3.4.24.7) and stromelysin was stimulated at all the corresponding concentrations. In contrast, human recombinant interleukin-1α (hrIL-1, 10 81127-A/asset/equation/feb2001457939081127a-math-si3.gif?v=1&s=d02546bf11b32933c027ccc0595659ec578d0c4c)
) coordinately induced these enzymes and TIMP production. The reduction of the elevated TIMP production by TNF was not due to the inhibition of TIMP secretion. These results suggest that TNF modulates the extracellular matrix degradation in human fibroblasts bifunctionally by the suppression of TIMP production in addition to the acceleration of matrix metalloproteinases production. Furthermore, the fact that TNF and IL-1 differently controlled the production of TIMP suggests that the signal pathway of TNF for TIMP production is different from that of IL-1.
