Epidermal growth factor (
EGF), which promotes epidermal
regeneration and
wound closure, is important for the proliferation and differentiation of epidermal and
epithelial tissues in
animals. Exogenous
EGF is a promising
therapeutic agent for
wound healing, but its general use is restricted by the limited availability of this
protein. In this
work, we show that the
transfection of
mouse BALB/MK
keratinocytes, which are totally dependent on
EGF for
growth and migration, with mature
cDNA for
human EGF via a retroviral vector abolished the
cells requirement for exogenous
EGF. The transformed
cells had normal morphology and a
growth rate that varied according to the source of the retroviral vector used.
Keratinocyte transfection with
EGF cDNA provides a
time- and
cost-efficient means of culturing
keratinocytes and yields
cells that may be useful for
skin grafting.