Evidence indicates that the neurotrophin nerve growth factor (NGF) is
a mediator of cutaneous inflammatory responses, Cellular responses to
NGF are facilitated by two receptors called trk A and p75 neurotrophin
receptor (p75(NTR)), In the current study we have investigated the ex
pression of these receptors in lesional and non-lesional skin from pat
ients with plaque psoriasis and in normal skin exposed to three times
the minimal erythema dose of ultraviolet (UV) B radiation, Trk a immun
ostaining was confined to the basal keratinocytes in normal skin. Ther
e was a significant reduction in trk A immunostaining in both non-lesi
onal and lesional psoriatic skin compared with control skin. In UVB-ir
radiated normal skin, there was a significant reduction in trk A immun
ostaining at 4 h after irradiation, which was still evident at 48 h, I
n normal skin, p75(NTR) immunopositive fine nerve fibres were present
throughout the dermis and occasionally seen in the epidermis. Thick ne
rve fibres were evident in the deep dermis and in the middle region of
the dermis, p75(NTR) immunopositive basal keratinocytes were occasion
ally seen. There was a statistically significant loss of p75(NTR) immu
nopositive fine nerve fibres in the epidermis of lesional psoriatic sk
in and a statistically significant loss of p75(NTR) immunopositive fin
e nerve fibres in the dermis in both nonlesional and lesional psoriati
c skin. p75(NTR) immunopositive thick nerve fibres were reduced in les
ional psoriatic skin compared with normal skin. UVB irradiation of nor
mal skin led to a statistically significant decrease in the p75(NTR) i
mmunopositive fine nerve fibres in the epidermis at 48 h after irradia
tion. There was no significant reduction in the dermal p75(NTR) immuno
reactivity. These results demonstrated that expression of both NGF rec
eptors is decreased following an acute inflammatory stimulus and also
in association with a chronic inflammatory dermatosis.