M. Horvath et al., POSTNATAL-DEVELOPMENT OF GAP-43 IMMUNOREACTIVITY IN THE AUDITORY BRAIN-STEM OF THE RAT, Journal of comparative neurology, 382(1), 1997, pp. 104-115
Extensive data link the growth associated protein GAP-43 to axonal elo
ngation and synapse formation during development and in plastic respon
ses of nervous tissue. We have studied the changing levels of GAP-43 e
xpression in the auditory brainstem nuclei of the developing rat by ap
plying immunocytochemical techniques. By the first postnatal day (P1),
GAP-43 was expressed at high concentrations in all subdivisions of th
e cochlear nuclear complex and the superior olivary complex. At this s
tage, neuropil structures recognized by the antibody did not show any
varicosities on cellular processes in all these regions. By P8, the te
xture of the stain has turned markedly more granular, a pattern likely
to reflect the formation of presynaptic endings. A predominantly gran
ular distribution of GAP-43 has developed by P12. At that time, the st
aining intensity is markedly reduced compared to the levels of the new
born. By P16, the auditory brainstem nuclei have lost most of their GA
P-43 immunoreactivity, but a distinct level of staining persisted into
adulthood in all of them. This staining was restricted to boutons, wh
ich are thought to be presynaptic terminals. We conclude that a modera
te but apparently relevant potential for plasticity is retained in the
se auditory structures. Should the patterns of neural signals, mediate
d by the inner ear, change during adulthood, the central structures ap
pear to be able to respond with the formation of altered synaptic conn
ectivity. (C) 1997 Wiley-Liss. Inc.