LESION-SPECIFIC PATTERN OF IMMUNOCYTOCHEMICAL DISTRIBUTION OF GROWTH-ASSOCIATED PROTEIN B-50 (GAP-43) IN THE CEREBELLUM OF WEAVER AND PCD-MUTANT MICE - LACK OF B-50 INVOLVEMENT IN NEUROPLASTICITY OF PURKINJE-CELL TERMINALS
J. Baurle et al., LESION-SPECIFIC PATTERN OF IMMUNOCYTOCHEMICAL DISTRIBUTION OF GROWTH-ASSOCIATED PROTEIN B-50 (GAP-43) IN THE CEREBELLUM OF WEAVER AND PCD-MUTANT MICE - LACK OF B-50 INVOLVEMENT IN NEUROPLASTICITY OF PURKINJE-CELL TERMINALS, Journal of neuroscience research, 38(3), 1994, pp. 327-335
The growth-associated protein B-50 (GAP-43) is thought to play a major
role in the development and regeneration of neurons. The participatio
n of B-50 in neuronal plasticity is well documented, especially for mo
noaminergic systems, However, such an important role for B-50 in GABAe
rgic systems has not been substantiated to date. This study was perfor
med to obtain detailed information about the identity of B-50 immunopo
sitive axons and terminals in the cerebellum and to test the involveme
nt of this protein during plastic changes as observed in the projectio
ns of GABAergic Purkinje cells to the lateral vestibular nucleus (LVN)
. For this purpose mutant mice with specific cerebellar cell loss were
used, Weaver mutants (B6CBA wv/wv), PCD-mutants (B6C3Fe pcd/pcd), and
their corresponding wild-type mice were investigated with immunocytoc
hemical and immunoblot procedures at the age of 8-23 days and 5-6 mont
hs using polyclonal and monoclonal antibodies to B-50. Substantial dif
ferences in B-50 distribution were detected between normals and mutant
s and between young and adult animals. These results demonstrate that
the labeling of B-50 is mainly related to the outgrowth of parallel fi
bers and to a minor degree on the ingrowth of non-GABAergie cerebellar
afferents. There was no immunocytochemical indication that B-50 is re
lated to Purkinje cells or accompanies the plasticity of the GABAergic
innervation of the LVN. (C) 1994 Wiley-Liss, Inc.