Hepatocyte growth factor (HGF) is one of the vital factors for wound healing. HGF expression markedly increases in wounded skin and is mainly localized in dermal fibroblasts. HGF expression level in human dermal fibroblasts in vitro, however, is low and thus may be stimulated by some factors in the process of wound healing. Candidates of the factors are inflammatory cytokines released by polymorphonuclear and mononuclear cells infiltrating the wounded area, but HGF production in human dermal fibroblasts is only slightly induced by interleukin (IL)-1, tumor necrosis factor (TNF)-α or interferon (IFN)-γ. We here report that a combination of IL-1β and IFN-γ or a combination of TNF-α and IFN-γ very markedly induced HGF production. The synergistic effect of the former was more marked than that of the latter. Synergistic effects of IL-1β and IFN-γ were observed at more than 10pg/ml and 10IU/ml, respectively, and were detectable as early as 12h after addition. Neither IFN-α nor IFN-β was able to replace IFN-γ. HGF mRNA expression was also synergistically upregulated by IL-1β and IFN-γ. IL-1β plus IFN-γ-induced synergistic production of HGF was potently inhibited by treatment of cells with the extracellular signal-regulated kinase (ERK) kinase inhibitor PD98059 and the p38 inhibitor SB203580 but not by the c-Jun N-terminal kinase (JNK) inhibitor SP600125. Taken together, our results indicate that a combination of IL-1β and IFN-γ synergistically induced HGF production in human dermal fibroblasts and suggest that activation of ERK and p38 but not of JNK is involved in the synergistic effect.