During embryogenesis, the neurons of vertebrate sympathetic and sensor
y ganglia become dependent on neurotrophic factors, derived from their
targets, for survival and maintenance of differentiated functions. Ma
ny of these interactions are mediated by the neurotrophins NGF, BDNF,
and NT3 and the receptor tyrosine kinases encoded by genes of the trk
family. Both sympathetic and sensory neurons undergo developmental cha
nges in their responsiveness to NGF, the first neurotrophin to be iden
tified and characterized. Subpopulations of sensory neurons do not req
uire NGF for survival, but respond instead to BDNF or NT3 with enhance
d survival. In addition to their classic effects on neuron survival, n
eurotrophins influence the differentiation and proliferation of neural
crest-derived neuronal precursors. In both sympathetic and sensory sy
stems, production of neurotrophins by target cells and expression of n
eurotrophin receptors by neurons are correlated temporally and spatial
ly with innervation patterns. In vitro, embryonic sympathetic neurons
require exposure to environmental cues, such as basic FGF and retinoic
acid to acquire neurotrophin-responsiveness; in contrast, embryonic s
ensory neurons acquire neurotrophin-responsiveness on schedule in the
absence of these molecules.