Neurotrophins such as nerve growth factor (NGF) mediate their effects
through interactions with high-affinity tropomycin-related kinase (trk
) receptors. The present study employed a polyclonal antibody to chara
cterize the distribution of trk-immunoreactive neurons within the nonh
uman primate brain. Both young adult and aged cebus and rhesus monkeys
displayed trk-immunoreactive neurons within all subdivisions of the b
asal forebrain. Colocalization studies revealed that between 66% and 7
6% of trk-immunoreactive basal forebrain neurons also expressed immuno
reactivity for the low-affinity p75 NGF receptor, an excellent marker
for cholinergic basal forebrain cells. In this experiment, most single
-labeled basal forebrain neurons contained only trk immunoreactivity,
whereas 4% of basal;forebrain neurons expressed only the low-affinity
p75 NGF receptor. Scattered trk-immunoreactive neurons also were obser
ved within the caudate nucleus and putamen. Although dual-localization
studies with choline acetyltransferase (ChAT) were not performed, str
iatal neurons codistributed with ChAT-immunoreactive cells, and both t
ypes of cells were similar in size and morphology. This suggests that
trk immunoreactivity is expressed within cholinergic interneurons with
in the primate striatum. Finally, lightly stained trk-immunoreactive n
eurons were observed within the stratum oriens of the hippocampal form
ation and within the hypothalamus. These data indicate that both choli
nergic and, possibly, noncholinergic forebrain neurons express the pro
tein for the high-affinity trk. receptor, which transduces the signal
mediating the trophic effects of neurotrophins. In addition, the patte
rn of trk immunoreactivity was preserved in two aged (26 and 29 years
old) rhesus monkeys, suggesting that the expression of trk, for the mo
st part, is sustained throughout the lifetime of the organism. (C) 199
4 Wiley-Liss, Inc.