We have used in situ hybridization to visualize cells in the developin
g rat retina and optic nerve that express mRNAs encoding the A and B c
hains of platelet-derived growth factor (PDGF-A and PDGF-B), and the a
lpha and beta subunits of the PDGF receptor (PDGF-alphaR and PDGF-beta
R). We have also visualized PDGF-A protein in these tissues by immunoh
istochemistry. In the retina, PDGF-A mRNA is present in pigment epithe
lial cells, ganglion neurons and a subset of amacrine neurons. PDGF-A
transcripts accumulate in ganglion neurons during target innervation a
nd in amacrine neurons around the time of eye opening, suggesting that
PDGF-A expression in these cells may be regulated by target-derived s
ignals or by electrical activity. In the mouse retina, PDGF-A immunore
activity is present in the cell bodies, dendrites and proximal axons o
f ganglion neurons, and throughout the inner nuclear layer. PDGF-alpha
R mRNA is expressed in the retina by astrocytes in the optic fibre lay
er and by a subset of cells in the inner nuclear layer that might be M
uller glia or bipolar neurons. Taken together, our data suggest short-
range paracrine interactions between PDGF-A and PDGF-alphaR, the ligan
d and its receptor being expressed in neighbouring layers of cells in
the retina. In the optic nerve, PDGF-A immunoreactivity is present in
astrocytes but apparently not in the retinal ganglion cell axons. PDGF
-alphaR+ cells in the optic nerve first appear near the optic chiasm a
nd subsequently spread to the retinal end of the nerve; these PDGF-alp
haR+ cells are probably oligodendrocyte precursors (Pringle et al., 19
92). RNA transcripts encoding PDGF-B and PDGF-betaR are expressed by c
ells of the hyaloid and mature vascular systems in the eye and optic n
erve.