The jimpy mutation has been identified as a point mutation in the gene
coding for the major myelin proteolipid protein. The most prominent e
ffect of the mutation is an extreme reduction in central nervous syste
m myelin in affected mice. However, both oligodendrocytes and astrocyt
es, the two types of central nervous system macroglia, have been shown
to exhibit more subtle developmental and metabolic changes as a resul
t of the mutation. These include early death and proliferation abnorma
lities in jimpy oligodendrocytes, and hypertrophy, increased pH and ab
normal responses to high K+ in jimpy astrocytes. In the present study,
we examine the effect of the mutation on the cell cycle of astrocytes
. Using an immunocytochemical method to chart the percent of labeled m
itoses, we find the total cell cycle to be lengthened in jimpy astrocy
tes by 5-6 h, with increases in several different phases. Since there
is no evidence that astrocytes make myelin proteolipid protein, the re
sults support previous studies which suggest that this gene may code f
or other proteins playing an important role in the development of many
cell types.