A. Mihaly et al., EXPRESSION OF RAF SERINE THREONINE PROTEIN-KINASES IN THE CELL-BODIESOF PRIMARY SENSORY NEURONS OF THE ADULT-RAT/, Cell and tissue research, 285(2), 1996, pp. 261-271
We have used immunocytochemistry to examine the distribution of raf pr
otein kinases in sensory neurons of the adult rat. In lumbar and trige
minal sensory ganglia, cells of all size ranges appeared to be raf imm
unoreactive and this was confirmed by double labeling using subpopulat
ion specific markers. Almost all cells labeled with Griffonia simplici
folia IB4 (a small cell marker) or immunostained by using a large cell
marker (RT97) showed raf immunoreactivity. These two markers label ce
lls known to differ in their expression of neurotrophin receptors (trk
). Thus raf kinases are not confined to cells expressing only certain
trk subtypes. In the dorsal horn of the spinal cord, raf immunoreactiv
ity was present in scattered neurons. However, sensory axons identifie
d by IB4 histochemistry were devoid of raf immunostaining. Lectin-labe
led nerve fibers in the cornea, lower lip and glans penis were also no
t immunoreactive. Ligation of the sciatic nerve did not produce any ac
cumulation of raf immunoreactivity, confirming that raf kinases are no
t axonally transported to the peripheral processes of sensory neurons.
Surgical dissection of the sciatic nerve caused the normal homogeneou
s cytoplasmic raf immunoreactivity to be replaced in some cells by a s
taining concentrated predominantly under the plasma membrane. One poss
ibility is that this represents activation of raf in these cells.