B50/GAP-43 has been implicated in neural plasticity, development, and
regeneration. Several studies of axonally transported proteins in the
optic nerve have shown that this protein is synthesized by developing
and regenerating retinal ganglion cells in mammals, amphibians, and fi
sh. However, previous studies using immunohistochemistry to localize B
50/GAP-43 in retina have shown that this protein is found in the inner
plexiform layer in adults. Since the inner plexiform layer contains t
he processes of amacrine cells, ganglion cells, and bipolar cells to d
etermine which cells in the retina express B50/GAP-43, we have now use
d in situ hybridization to localize the mRNA that codes for this prote
in in the developing rat retina. We have found that B50/GAP-43 is expr
essed primarily by cells in the retinal ganglion cell layer as early a
s embryonic day 15, and until 3 weeks postnatal. Some cells in the inn
er nuclear layer, possibly a subclass of amacrine cells, also express
B50/GAP-43 protein and mRNA; however, the other retinal neurons-bipola
r cells, photoreceptors, and horizontal cells express little, if any,
B50/GAP-43 at any stage in their development. Early in development, th
e protein appears in the somata and axons of ganglion cells, while lat
er in development, B50/GAP-43 becomes concentrated in the inner plexif
orm layer, where it continues to be expressed in adult animals. These
results are discussed in terms of previous proposals as to the functio
ns of this molecule.