Background Several of the characteristic clinical features of photoaged ski
n, including wrinkling, are thought to be dependent on changes in the derma
l matrix brought about by chronic sun exposure. Such changes include reduct
ions in collagens I, III and VII, an increase in elastotic material in the
reticular dermis and a marked reduction in the microfibrillar glycoprotein
fibrillin.
Objectives To examine whether type VI collagen, a microfibrillar collagen n
ecessary for cell-cell and cell-matrix communication, is affected by the ph
otoageing process.
Methods Six healthy volunteers with moderate to severe photoageing were enr
olled into the study. Immunohistochemistry and in situ hybridization histoc
hemistry were used to examine the levels of type VI collagen in photoprotec
ted and photoaged sites.
Results In photoprotected skin, type VI collagen was concentrated in the pa
pillary dermis immediately below the dermal-epidermal junction, around bloo
d vessels, hair follicles and glandular structures. The distribution of typ
e VI collagen was unchanged in photoaged skin, although we observed an incr
ease in the abundance of the alpha3 chain of collagen VI in the upper papil
lary dermis, at its junction with the dermal-epidermal junction (P < 0.05).
No alterations were observed for any a chain at the mRNA level.
Conclusions These studies suggest that chronic sun exposure (photoageing) h
as little or no effect on either the distribution, abundance or levels of e
xpression of type VI collagen in human skin. Thus, type VI collagen, unlike
other matrix components so far studied, appears to be relatively unaffecte
d by the photoageing process.