The function of keratinocyte growth factor (KGF) in normal and wounded
skin was assessed by expression of a dominant-negative KGF receptor t
ransgene in basal keratinocytes. The skin of transgenic mice was chara
cterized by epidermal atrophy, abnormalities in the hair follicles, an
d dermal hyperthickening. Upon skin injury, inhibition of KGF receptor
signaling reduced the proliferation rate of epidermal keratinocytes a
t the wound edge, resulting in substantially delayed reepithelializati
on of the wound.