DEVELOPMENTAL PATTERNS OF PROTEOGLYCAN-CONTAINING EXTRACELLULAR-MATRIX IN PERINEURONAL NETS AND NEUROPIL OF THE POSTNATAL RAT-BRAIN

Citation
G. Koppe et al., DEVELOPMENTAL PATTERNS OF PROTEOGLYCAN-CONTAINING EXTRACELLULAR-MATRIX IN PERINEURONAL NETS AND NEUROPIL OF THE POSTNATAL RAT-BRAIN, Cell and tissue research, 288(1), 1997, pp. 33-41
Citations number
60
Categorie Soggetti
Cell Biology
Journal title
ISSN journal
0302766X
Volume
288
Issue
1
Year of publication
1997
Pages
33 - 41
Database
ISI
SICI code
0302-766X(1997)288:1<33:DPOPE>2.0.ZU;2-4
Abstract
The extracellular matrix is involved in various morphogenetic processe s which are accompanied by changes in its physicochemical properties a nd spatial organization. In the adult brain it contributes to cellular communication and the regulation of neuronal activity. The present st udy deals with the postnatal appearance and transformation into adult distribution patterns of extracellular matrix components related to ch ondroitin-sulphate proteoglycans (CSPGs) in the rat brain. The differe ntial accumulation of these components in neuropil and in perineuronal nets (PNs) enriched in certain regions was examined in 0-, 7-, 14-, 2 1- and 35-day-old rats and adult animals using the N-acetylgalactosami ne-binding Wisteria floribunda agglutinin (WFA) and immunocytochemical detection of CSPGs. The lectin stained the olfactory-bulb glomerular layer and layer Ia of piriform and entorhinal cortex already in newbor n animals. On postnatal day 7 diffuse neuropil staining was additional ly found in certain subcortical nuclei and in deep neocortical layers. The first sharply contoured PNs were detected at this age in the brai n stem, indicating the more advanced maturation of matrix components i n subcortical regions. CSPG immunoreactivity yielded staining patterns largely identical to WFA-binding patterns but appeared only between p ostnatal day 14 and 21. The adult-like stage was revealed with both me thods between 21 and 35 days after birth. The results provide further evidence that the accumulation of certain CSPGs in the extracellular s pace is spatiotemporally related to distinct patterns of neuronal acti vity at the regional and cellular level.