Nerve growth factor (NGF) binding to cellular receptors is required fo
r the survival of some neural cells. In contrast to Trk A, the high-af
finity NGF receptor that transduces NGF signals for survival and diffe
rentiation, the function of the low-affinity NGF receptor, p75NGFR, re
mains uncertain. Expression of p75NGFR induced neural cell death const
itutively when p75NGFR was unbound; binding by NGF or monoclonal antib
ody, however, inhibited cell death induced by p75NGFR. Thus, expressio
n of p75NGFR may explain the dependence of some neural cells on NGF fo
r survival. These findings also suggest that p75NGFR has some function
al similarities to other members of a superfamily of receptors that in
clude tumor necrosis factor receptors, Fas (Apo-1), and CD40.