G. Alonso et al., IMMUNOLOCALIZATION OF B-50 (GAP-43) IN INTACT AND LESIONED NEUROHYPOPHYSIS OF ADULT-RATS, Experimental neurology, 131(1), 1995, pp. 93-107
The persistence of high levels of B-50 in the adult brain is generally
assumed to characterize neuronal systems capable of undergoing some f
orm of plasticity such as axonal sprouting and regeneration, Since adu
lt hypothalamo-neurohypophysial neurons are known to rapidly regenerat
e after being transected, the present study was undertaken to determin
e if such a capacity for regeneration could be related to the expressi
on of this protein. Adult rats were killed by intraaortic perfusion of
fixative either without lesion or at different delays after a surgica
l transection of the hypophysial stalk. Electron microscopy and laser
scanning confocal microscopy were used to examine the regenerating axo
ns after single or double immunocytochemical labeling of vibratome sec
tions for B-50 and for various neuronal markers characterizing differe
nt types of neurohypophysial axons, In intact neurohypophysis, B-50 im
munostaining was frequently associated with fibers immunoreactive to G
ABA or to tyrosine hydroxylase, whereas it was not detected within pep
tidergic neurohypophysial axons. In the lesioned neurohypophysis, B-50
was again frequently localized within axonal fibers immunoreactive to
tyrosine hydroxylase or GABA. On the other hand, B-50 immunostaining
was never detected within the numerous vasopressinergic or oxytocinerg
ic axonal sprouts that regenerate all along the median eminence proxim
al to the lesion. These data indicate that persistence of high levels
of B-50 within the neurohypophysis of adult rats is a specific feature
of catecholaminergic and/or GABA-ergic axons innervating this region
and that, contrasting to other neuronal systems, B-50 is not involved
in the remarkable capacity for regeneration exhibited by the vasopress
inergic and oxytocinergic neurohypophysial axons. (C) 1995 Academic Pr
ess, Inc.