Hepatocyte growth factor (HGF), also known as scatter factor (SF), is a motogen, mitogen and morphogen produced by mesenchymal cells that mainly acts on epithelial cells and is involved in osteoclast stimulation. This study examined the possible enhanced production of HGF=SF by human gingival ®broblasts upon stimulation with killed cells of Porphyromonas gingivalis strain 381 and its representative bioactive cellular components, ®mbriae and lipopolysaccharide (LPS). P. gingivalis whole cells enhanced the production of HGF=SF detected by ELISA in culture supernates of the ®broblasts. Fimbriae prepared from P. gingivalis exhibited powerful HGF=SF-inducing activity in a concentration-dependent manner, with peak activity observed at 100±200 ìg=ml. The ®mbriae-induced HGF=SF mRNA expression by the cells was also detected by reverse transcription-PCR. P. gingivalis LPS exhibited weak HGF=SF-inducing activity. The study also examined the HGF=SF-inducing activity of seven synthetic peptides corresponding to the segments of P. gingivalis ®mbrial subunit protein. The peptides of residues 282±301 and 302±321, which exhibited antagonistic effects against P. gingivalis ®mbriae-binding to human gingival ®broblasts in a previous study, showed weak activity, whereas other non-antagonistic peptides showed no signi®cant activity. These ®ndings indicated that P. gingivalis ®mbriae enhanced production of HGF=SF by human gingival ®broblasts, whereas synthetic peptide segments of ®mbrial subunit protein were not suf®cient to exert the activity.