Uncoordinate regulation of collagenase, stromelysin, and tissue inhibitor of metalloproteinases genes by prostaglandin E2: Selective enhancement of collagenase gene expression in human dermal fibroblasts in culture

✍ Scribed by Alain Mauviel; Cynthia Halcin; Panayiotis Vasiloudes; William C. Parks; Markku Kurkinen; Jouni Uitto

• Publisher: John Wiley and Sons
• Year: 1994
• Tongue: English
• Weight: 838 KB
• Volume: 54
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.240540413

✦ Synopsis

The degradative effects of interleukin-1 (IL-1) on the extracellular matrix of connective tissue are mediated primarily by metalloproteinases and prostaglandins. Clinical observations suggest that these effects can be prevented, to some extent, by the use of non-steroidal anti-inflammatory drugs. We have examined the role of prostaglandin E2 (PGE2) in IL-1 -induced gene expression by human skin fibroblasts in culture. Incubation of confluent fibroblast cultures with varying concentrations (0.01-1 . O &ml) of PGE2 led to a dose-dependent elevation of collagenase mRNA steady-state levels, the promoter activity, and the secretion of the protein, whereas relatively little effect was observed on stromelysin and TlMP gene expression. Exogenous PGE2 had no additive or synergistic effect with IL-1 on collagenase gene expression. Furthermore, commonly used non-steroidal anti-inflammatory drugs (indomethacin, acetyl salicylic acid and ibuprofen), at doses which block prostaglandin synthesis in cultured fibroblasts, failed to counteract IL-1 -induced collagenase and stromelysin gene expression, nor did they affect TlMP expression. Although the effects of PGE2 did not potentiate those of IL-I on collagenase gene expression in vitro, one could speculate that massive production of PGE2 by connective tissue cells in vivo in response to inflammatory mediators such as IL-1 or tumor necrosis factor-a, could lead to sustained expression of collagenase in connective tissue cells after clearance of the growth factors.