The molecular mechanisms necessary for remyelination by oligodendrocyt
es remain unexplored. We previously characterized a myelin basic prote
in promoter-lacZ (MBP-lacZ) transgene whose expression is regulated un
iquely during development and also in pathological situations, suggest
ing that it may be a useful reporter of molecular mechanisms during re
myelination. As a first step toward creating a transgenic mouse model
of remyelination, we cultured oligodendrocytes from these transgenic m
ice and showed that expression of MBP-lacZ appeared in parallel with a
marker of oligodendrocyte maturation, galactocerebroside (GC). In add
ition, basic fibroblast growth factor blocked the expression of both M
BP-lacZ and GC in these cells. Therefore, expression of MBP-lacZ refle
cts not only the developmental stage of oligodendrocytes, but also ext
rinsic influences on oligodendrocytes. These data suggest that MBP-lac
Z may be a useful marker in transgenic mouse models of remyelination.