LESION-INDUCED EXPRESSION OF LOW-AFFINITY NGF-BINDING PROTEIN (P75) IMMUNOREACTIVITY AFTER NEONATAL AND ADULT ASPIRATION LESIONS OF THE RATDORSOMEDIAL PREFRONTAL CORTEX
Cg. Vaneden et A. Rinkens, LESION-INDUCED EXPRESSION OF LOW-AFFINITY NGF-BINDING PROTEIN (P75) IMMUNOREACTIVITY AFTER NEONATAL AND ADULT ASPIRATION LESIONS OF THE RATDORSOMEDIAL PREFRONTAL CORTEX, Developmental brain research, 82(1-2), 1994, pp. 167-174
The present study was performed in order to examine whether or not NGF
-mediated processes could be involved in the sparing of function obser
ved after neonatal prefrontal cortex lesions. After unilateral neonata
l aspiration lesions of the dorsomedial prefrontal cortex, fibers immu
noreactive for the low-affinity NGF-binding protein (p75) with a devia
nt morphology were observed in the severed hemisphere only. The morpho
logy of these fibers was characterized by their large caliber, their l
arge, often bulbous varicosities, and their curly appearance. These fi
bers were present as soon as 24 h after the operation. Between 3 and 5
days after the operation, the greatest abundance of these fibers was
found in the ventrorostral areas of the forebrain and along the pathwa
ys of cortical projections of the cholinergic cell groups. After 7 day
s, such fibers were no longer observed. After comparable lesions in ad
ult animals, a similar type of fiber was observed in the lesioned hemi
sphere. However, in these cases a response comparable to that observed
in the neonatal animals was not observed until 5 days after the opera
tion, with fewer fibers. Furthermore, in contrast to what was observed
after neonatal lesions, in adult animals no indications of retrograde
transport of p75 immunoreactive material towards the cholinergic cell
s of the basal forebrain nuclei were found. From these findings it was
concluded that the prompt upregulation of p75 expression in neonatal
animals may contribute to the survival of the cholinergic cells of the
basal forebrain, and may therefore be involved in the restoration of
function of the medial prefrontal cortex.