We describe a major glial cell population in the central nervcus system (CN
S) that can be identified by the expression of 2 cell surface molecules, th
e NG2 proteoglycan and the alpha receptor for platelet-derived growth facto
r (PDGF alpha R). In vitro and in the developing brain in vivo, NG2 and PDG
F alpha R are expressed on oligodendrocyte progenitor cells but are down-re
gulated as the progenitor cells differentiate into mature oligoder drocytes
. In the mature CNS, numerous NG2+/PDGF alpha R+ cells with extensive arbor
ization of their cell processes are found ubiquitously long after oligodend
rocytes are generated. NG2+ cells in the mature CNS do not express antigens
specific to mature oligodendrocytes, astrocytes, microglia, or neurons, su
ggesting that they are a novel population of glial cells. Recently NG2+ cel
ls in the adult CNS have been shown to undergo proliferation and morphologi
cal changes in response to a variety of stimuli, such as demyelination and
inflammation, suggesting that they are dynamic cells capable of responding
to changes in the environment. Furthermore, high levels of NG2+ and PDGF al
pha R are expressed on oligodendroglioma cells, raising the possibility tha
t the NG2+/PDGF alpha R+ cells in the mature CNS contribute to glial neopla
sm.