MOSAIC DISTRIBUTION OF CHONDROITIN AND KERATAN SULFATE IN THE DEVELOPING RAT STRIATUM - POSSIBLE INVOLVEMENT OF PROTEOGLYCANS IN THE ORGANIZATION OF THE NIGROSTRIATAL SYSTEM
I. Charvet et al., MOSAIC DISTRIBUTION OF CHONDROITIN AND KERATAN SULFATE IN THE DEVELOPING RAT STRIATUM - POSSIBLE INVOLVEMENT OF PROTEOGLYCANS IN THE ORGANIZATION OF THE NIGROSTRIATAL SYSTEM, Developmental brain research, 109(2), 1998, pp. 229-244
The striatum of the mammalian basal ganglia is composed of two neuroch
emically distinct compartments termed patches and matrix that contribu
te overall to a mosaic organization. Glycosaminoglycans (GAGs), the su
gar moieties of proteoglycans, provide specific spatio-temporal guidan
ce cues during the development of several functional neural systems. H
owever, their distribution within the nigrostriatal system has not bee
n investigated yet. Here, the immunohistochemical distributions of uns
ulphated (COS), 4-sulphated (C4S) and 6-sulphated chondroitin (C6S) an
d keratan sulphate (KS) were examined in the developing neostriatum of
rat and compared with the distribution of dopaminergic terminals. All
the chondroitin sulphate (CS) isomers are homogeneously expressed in
the embryonic striatum. After birth, COS and C6S reveal the striatal m
osaic in being preferentially expressed within the matrix compartment
and in boundaries around patches whereas the C4S epitope is present in
both compartments, with a slight patchy distribution. KS expression i
s detected first in the patches during the early postnatal period and
subsequently only in the matrix compartment. All these GAG expressions
disappear as the brain matures except for C4S which remains high thro
ughout adult life. Furthermore, studies within the developing medial f
orebrain bundle reveal that CS isomers, but not KS, are expressed in a
nd around the dopamine axonal tract but show similar developmental pat
terns of distribution which do not appear to be specifically associate
d with the nigrostriatal pathway. These results suggest a possible imp
lication of proteoglycans during the development of the striatum and m
ay be useful for understanding the complex cellular and molecular inte
ractions in degeneration and plasticity of the nigrostriatal circuit i
n Parkinson's disease. (C) 1998 Elsevier Science B.V. All rights reser
ved.