Cc. Stichel et al., DIFFERENTIAL EXPRESSION OF THE SMALL CHONDROITIN DERMATAN SULFATE PROTEOGLYCANS DECORIN AND BIGLYCAN AFTER INJURY OF THE ADULT-RAT BRAIN/, Brain research, 704(2), 1995, pp. 263-274
Chondroitin sulfate proteoglycans are widespread extracellular matrix
proteins and are specifically upregulated after CNS injury at the lesi
on site. Many proteoglycan core proteins have been described in the ra
t brain, but detailed analysis of individual proteoglycans expressed a
fter injury are missing. The present study represents an initial attem
pt to assess the diversity and timing of lesion-induced expression of
proteoglycans in order to elucidate their functional role in CNS injur
y and repair. Using immunocytochemical methods we analysed the express
ion of decorin and biglycan in the transected postcommissural fornix o
f the adult rat. Transection of the fornix induced the upregulation of
both decorin and biglycan. However, their expression differed with re
spect to time course, regional extent and cellular localization. The r
apid upregulation of decorin within a wide area around the lesion was
followed by a massive appearance of biglycan that remained restricted
to the transection site. Three months after lesion, differences of the
area size of decorin- and biglycan-immunoreactivities were no longer
detectable. Both proteoglycans were restricted to the lesion site and
the fornix stumps. While decorin was primarily expressed by astrocytes
, biglycan was deposited extracellularly in sheet-like structures. The
upregulation of both proteoglycans persisted for at least up to 6 mon
ths after lesion. These strong but divergent lesion-induced expression
patterns indicate important but different roles of decorin and biglyc
an in CNS injury.