M. Steinhoff et al., Proteinase-activated receptor-2 in human skin: tissue distribution and activation of keratinocytes by mast cell tryptase, EXP DERMATO, 8(4), 1999, pp. 282-294
Proteinase-activated receptor-2 (PAR-2) is a G-protein coupled receptor. Tr
yptic proteases cleave PAR-2 exposing a tethered ligand (SLIGKV), which bin
ds and activates the receptor. Although PAR-2 is highly expressed by cultur
ed keratinocytes and is an inflammatory mediator, its precise localization
in the normal and inflamed human skin is unknown, and the proteases that ac
tivate PAR-2 in the skin have not been identified. We localized PAR-2. in h
uman skin by immunohistochemistry, examined PAR-2 expression by RT-PCR and
RNA blotting, and investigated PAR-2 activation by mast cell tryptase. PAR-
2 was localized to keratinocytes, especially in the granular layer, to endo
thelial cells, hair follicles, myoepithelial cells of sweat glands, and der
mal dendritic-like cells. PAR-2 was also highly expressed in keratinocytes
and endothelial cells of inflamed skin. PAR-2 mRNA was detected in normal h
uman skin by RT-PCR, and in cultured human keratinocytes and dermal microva
scular endothelial cells by Northern hybridization. Trypsin, tryptase and a
peptide corresponding to the tethered ligand (SLIGKVNH(2)) increased [Ca2](i) in keratinocytes, measured using Fura-2/AM. Although tryptase-containi
ng mast cells were sparsely scattered in the normal dermis, they were numer
ous in the dermis in atopic dermatitis, and in the dermis, dermal-epidermal
border, and occasionally within the lower epidermis in psoriasis. Tryptase
may activate PAR-2 on keratinocytes and endothelial cells during inflammat
ion.