The survival of neurons in the developing isthmo-optic nucleus (ION) i
s believed to depend on the retrograde transport of trophic molecules
from the target, the contralateral retina. We now show that ION neuron
s transport nerve growth factor (NGF), brain-derived neurotrophic fact
or (BDNF), and neurotrophin-3 (NT-3) retrogradely and that BDNF and NT
-3 support the survival of ION neurons in vivo and promote neurite out
growth in vitro. Surprisingly, NGF enhanced normal developmental cell
death in vivo in a dose-dependent way. These findings show that increa
sed levels of NGF can have adverse effects on differentiated neurons.
The negative effect of NCF could be mimicked by intraocular injection
of antibodies that block binding of neurotrophins to the 75 kd neurotr
ophin receptor (p75). These data implicate a role for the p75 receptor
in NCF's neurotoxicity and indicate that this receptor is involved in
the mechanism by which ION neurons respond to BDNF and NT-3 in the ta
rget.