GLYCEROPHOSPHORYLCHOLINE PHOSPHOCHOLINE PHOSPHODIESTERASE ACTIVITY DURING THE DIFFERENTIATION OF GLIAL PROGENITOR CELLS

Citation
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
Citations number
15
Categorie Soggetti
Neurosciences
ISSN journal
03604012
Volume
36
Issue
4
Year of publication
1993
Pages
441 - 445
Database
ISI
SICI code
0360-4012(1993)36:4<441:GPPAD>2.0.ZU;2-Y
Abstract
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.