The introduction and expression of a foreign gene provide a powerful tool f
or investigating functions and regulation of a gene of interest; however, k
eratinocytes have a major drawback in that foreign genes are hardly transfe
cted by conventional methods and stable transformants are most difficult to
establish in normal keratinocytes with a limited short life span. To overc
ome these problems, we used an adenovirus vector, Ax, developed by Saito et
al, which yields desired recombinant viruses at an efficiency about 100-fo
ld that of conventional methods, and by which genes are expressed at a high
level under the control of a composite CAG promoter. We established Ax vec
tors carrying various isoforms of protein kinase C (PKC), Using these vecto
rs, we found that the eta and delta isoforms of PKC, but not the alpha and
zeta isoforms, mediate terminal differentiation in normal human keratinocyt
es. These Ax-vectors are also applicable to organ culture of mouse embryos.
Advantages and disadvantages of adenovirus vectors and their use for kerat
inocyte biology are reviewed.