M. Chen et al., ULTRAVIOLET-A IRRADIATION UP-REGULATES TYPE-VII COLLAGEN EXPRESSION IN HUMAN DERMAL FIBROBLASTS, Journal of investigative dermatology, 108(2), 1997, pp. 125-128
Type VII collagen, a major component of skin-anchoring fibrils, is syn
thesized by both fibroblasts and keratinocytes, the two principal cell
types in the skin, In this study, we examined the effects of ultravio
let A (UVA) irradiation on the expression of type VII collagen in huma
n fibroblasts. UVA irradiation (0-15 J/cm(2)) caused a dose-dependent
increase (5- to 10-fold) in type VII collagen mRNA levels as detected
by northern blot analysis, The UVA-induced enhancement of type VII col
lagen gene expression correlated with an increase in its protein level
by immunoblot analysis of proteins secreted into the conditioned medi
um. The effect of UVA was observed at 12 h and reached its maximum by
18 h Under these conditions, however, the expression of fibronectin, a
major dermal matrix protein, remained unchanged, suggesting that the
induction of type VII collagen expression was selective, Actinomycin D
, a transcription inhibitor, blocked the UVA-mediated induction of typ
e VII collagen gene expression, whereas cycloheximide, a protein synth
esis inhibitor, superinduced the expression of type VII collagen, sugg
esting that ne novo protein synthesis was not required for the action
of UVA, Interestingly, in contrast to the increased type VII collagen
expression in fibroblasts in response to UVA, a slight decrease in typ
e VII collagen mRNA level was observed in the UVA-irradiated keratinoc
ytes, suggesting that the effect of UVA on the type VII collagen expre
ssion is cell type specific.