CHANGES IN THE EXPRESSION OF THE EXTRACELLULAR-MATRIX MOLECULES TENASCIN-C AND TENASCIN-R AFTER 3-ACETYLPYRIDINE-INDUCED LESION OF THE OLIVOCEREBELLAR SYSTEM OF THE ADULT-RAT
Es. Wintergerst et al., CHANGES IN THE EXPRESSION OF THE EXTRACELLULAR-MATRIX MOLECULES TENASCIN-C AND TENASCIN-R AFTER 3-ACETYLPYRIDINE-INDUCED LESION OF THE OLIVOCEREBELLAR SYSTEM OF THE ADULT-RAT, European journal of neuroscience, 9(3), 1997, pp. 424-434
In the central nervous system of rodents, the extracellular matrix gly
coproteins tenascin-C and tenascin-R are expressed predominantly by as
trocytes and oligodendrocytes respectively. Both molecules support neu
rite outgrowth from several neuronal cell types when presented as unif
orm substrates. When offered as a sharp boundary with a permissive sub
strate, however, both molecules prevent neurite elongation. On the bas
is of these observations it has been suggested that tenascin-C and ten
ascin-R may be relevant in determining the cellular response after inj
ury in the adult rodent central nervous system. To investigate whether
tenascin-C and tenascin-R may play important functional roles in the
lesioned central nervous system, we have analysed their expression in
the olivocerebellar system of the adult rat after 3-acetylpyridine-ind
uced degeneration of nerve cells in the inferior olivary nucleus. Tena
scin-C mRNA was not detectable at any time in the unlesioned or lesion
ed inferior olivary nucleus by in situ hybridization. In the cerebella
r cortex, tenascin-C mRNA in Golgi epithelial cells was down-regulated
3 days after the lesion and returned to control values 80 days after
the lesion. Tenascin-R mRNA was expressed by distinct neural cell type
s in the unlesioned olivocerebellar system. After a lesion, the densit
y of cells containing tenascin-R transcripts increased significantly i
n the inferior olivary nucleus and in the white matter of the cerebell
ar cortex. Immunohistochemical and immunochemical investigations confi
rmed these observations at the protein level. Our data thus suggest di
fferential functions of tenascin-C and tenascin-R in the injured centr
al nervous system.