Members of the death receptor family may play a prominent role in developme
ntal and pathological neuronal cell death. We report the expression of the
TR3 and TR7 death receptors in the adult human and rat central nervous syst
em. Whereas expression of TR3 appears to be high in the human cerebellum, w
ith lower levels in other brain regions, robust expression is observed in m
any regions of the rat brain. We also analysed modulation of death receptor
expression in an in vivo rat model of acute stroke. In contrast to tumour
necrosis factor receptor 1, Fas and p75(NGFR), which all show up-regulation
specifically in lesioned cortex of the permanent middle cerebral artery oc
clusion model of stroke, TR3 shows a rapid global increase in both lesioned
and unlesioned brain. In comparison, the recently described death receptor
TR7 shows no change in this model. These data indicate that the death rece
ptors show clear differences in patterns of expression in response to ischa
emic injury. (C) 2000 IBRO. Published by Elsevier Science Ltd.