Keratinocyte growth factor (KGF) is the seventh member of the fibroblast gr
owth factor (FGF) family. It is produced by mesenchymal cells and its activ
ity is specific for epithelial cell, controlling epithelial homeostasis and
wound repair in a paracrine manner. Although KGF has been implicated in a
number of hyperplastic pathologies, it has not previously been investigated
in gingival hyperplasia (GH), an adverse side-effect of three pharmacologi
cally different types of drugs, including the anti-hypertensive drug nifedi
pine (NIF), The mechanism by which NIF causes GH is not yet known, but we h
ave recently shown that KGF mRNA transcripts are elevated in drug-induced G
H in vivo (manuscript submitted). It is therefore possible that the action
of NIF is mediated via KGF and, in the present study, using the enzyme-link
ed immunosorbent assay (ELISA) and the semi-quantitative reverse transcribe
d-polymerase chain reaction (RT-PCR), we found that NIF upregulates KGF sec
retion and gene transcription by gingival fibroblasts in vitro. Our results
thus suggest that KGF may have an important role in the molecular patholog
y of GH in vivo. (C) 2000 Academic Press.