M. Monge et al., GLYCEROPHOSPHORYLCHOLINE PHOSPHOCHOLINE PHOSPHODIESTERASE ACTIVITY DURING THE DIFFERENTIATION OF GLIAL PROGENITOR CELLS, Journal of neuroscience research, 36(4), 1993, pp. 441-445
O-2A progenitor cells were grown in medium containing either 1% or 10%
fetal calf serum (FCS) for 4 weeks. The cells in 1% FCS were 75% olig
ondendrocytes by 3 weeks in culture. The cell population was so overgr
own with astrocytes in the 10% medium that an accurate estimate of cel
l number could not be made. The activities of glycerophosphorylcholine
phosphocholine phosphodiesterase (GPC-PC-PdE), p-nitrophenylphosphory
lcholine phosphodiesterase (pNPPC-PC-PdE), and ceramide UDP galactose
galactosyl transferase (CGalT) were barely detectable in the cells gro
wn in 10% FCS. The activities of these 3 enzymes were low in the cells
grown in 1% FCS for the first 2 weeks and then all 3 increased manyfo
ld. These observations reinforce the evidence previously accrued showi
ng that these two phosphodiesterase activities (GPC-PC-PdE and pNPPC-P
C-PdE) are markers of oligodendroglial cells as well as myelin. In con
trast, glycerophosphorylcholine choline phosphodiesterase (GPC-C-PdE)
activities were present in cells grown in both 1% and 10% FCS. (C) 199
3 Wiley-Liss, Inc.