We have examined the hypothesis that the segregation of LGN axon termi
nals into ocular dominance (OD) patches in layer 4 of the visual corte
x requires neurotrophins, acting as signals to modulate the pattern of
synaptic connectivity. Neurotrophin receptor antagonists, composed of
the extracellular domain of each member of the trk family of neurotro
phin receptors fused to a human Fc domain, were infused directly into
visual cortex during the peak phase of OD column formation. Infusion o
f trkB-IgG, which binds BDNF and NT-4/5, inhibited the formation of OD
patches within layer 4, while trkA-IgG and trkC-IgG, which preferenti
ally bind NGF and NT-3, respectively, had no effect. The autoradiograp
hic labeling of LGN terminals in cortical layer 4 was reduced by trkB-
IgG, in contrast with the increased labeling observed following NT-4/5
infusion. These data suggest that an endogenous ligand of trkB, norma
lly present in limiting amounts within visual cortex, is necessary for
the selective growth and remodeling of LGN axons into eye-specific pa
tches.