The sensory neurons of the nodose ganglion are the classic example of a pop
ulation of peripheral nervous system neurons that do not require nerve grow
th factor (NGF) for survival during development but are dependent on other
neurotrophins. We have re-examined this assertion by studying the developme
nt of the nodose ganglion of mice that have a null mutation in the NGF gene
. Compared with wild-type embryos, the number of neurons undergoing apoptos
is was elevated in NGF(-/-) mice, resulting in a significant reduction in t
he total number of neurons in the ganglion by the end of embryonic developm
ent. TrkA, the NGF receptor tyrosine kinase, was expressed in the nodose ga
nglion throughout development and there was a marked decrease in TrkA mRNA
expression in the nodose ganglion of NGF(-/-) embryos. Although the in vitr
o survival of the majority of nodose neurons was promoted by brain-derived
neurotrophic factor (BDNF), a minor proportion was supported by NGF in cult
ures established over a range of embryonic stages. These results clearly de
monstrate that a subset of nodose ganglion neurons depends on NGF for survi
val during development. The finding that the expression of tyrosine hydroxy
lase (TH) mRNA was unaffected in the nodose ganglia of NGF-deficient embryo
s indicates that this NGF-dependent subset is distinct from the subset of c
atacholaminergic neurons in the nodose ganglion.