Ultraviolet-B irradiation of human dermal fibroblasts has earlier been shown to induce matrix-degrading metalloproteinases, thus driving connective tissue degradation in photoaging and photocarcinogenesis. Herein,,vc report that Ultraviolet-B irradiation led to a dramatic increase in specific mRNA and protein levels of interstitial collagenase, stromelysin and interleukin-6. By contrast, the major tissue inhibitor of matrix-degrading metalloproteinases, TIMP-1, was unaffected, Monospecific neutralizing antibodies directed against human interleukin-6 significantly reduced the interstitial collagenase and stromelysin-1 protein levels, Taken together, our data provide the first evidence that Ultraviolet-B induction of interstitial collagenase and stromelysin-l occurs, ia the synthesis and release of interleukin-6. Hence, this newly identified autocrine mechanism may contribute to dermal photodamage. (C) 1999 Federation of European Biochemical Societies.