J. Gailit et al., TGF-BETA-1 STIMULATES EXPRESSION OF KERATINOCYTE INTEGRINS DURING REEPITHILIALIZATION OF CUTANEOUS WOUNDS, Journal of investigative dermatology, 103(2), 1994, pp. 221-227
Epidermal keratinocytes migrate over a provisional matrix during the r
e-epithelialization of cutaneous wounds. We have investigated the expr
ession of integrins and of transforming growth factor-beta 1 (TGF-beta
1) during re-epithelialization in a porcine model. Tissue specimens w
ere collected at different times after injury and stained with antibod
ies against subunits of the fibronectin receptor, integrin alpha 5 bet
a 1, and the vitronectin receptor, integrin alpha v beta 5. Intense st
aining was observed in the migrating keratinocytes of 5-d wounds; basa
l and suprabasal cells were stained around the entire cell periphery.
Staining returned toward normal levels in 14-d wounds. The appearance
of the extracellular form of TGF-beta 1 seemed to be coordinated with
the increased expression of integrin subunits: it was detected in migr
ating keratinocytes and in the adjacent epidermis of early wounds at 5
and 7 d. We also investigated the effect of TGF-beta 1 on cultured ep
idermal cells. Treating human keratinocytes with TGF-beta 1 increased
the levels of mRNA for the integrin subunits alpha 5, alpha v, and bet
a 5, but had little effect on beta 1. The corresponding cell-surface e
xpression of alpha 5 and alpha v was also increased after treatment. T
hus, during wound repair, TGF-beta 1 may induce epidermal keratinocyte
s to express integrins that facilitate the migratory component of re-e
pithelialization.