We investigated the onset of expression of the myelin/oligodendrocyte
glycoprotein (MOG) mRNA and protein in the developing mouse central ne
rvous system. In situ hybridization on brain sections at different sta
ges of embryonic and postnatal development showed that MOG transcripts
were first detected at birth in the medulla oblongata. During the fir
st week after birth, cells expressing MOG mRNA were located in the ven
tral longitudinal funiculus. During the second postnatal week, the pat
tern of MOG mRNA expression extended rostrally to the mid-forebrain re
gions and reached completion by the beginning of the third week. MOG t
ranscription was delayed by several days with respect to myelin basic
protein (MBP), and it appeared that while the MBP probe labeled both n
on-myelinating and myelinating oligodendrocytes, only the latter were
MOG-positive. In vitro, immunocytochemical analysis of MOG protein exp
ression, performed on myelinating cultures derived from mouse brain em
bryos at 15 days of gestation, confirmed the strict restriction of MOG
expression to myelinating oligodendrocytes. In particular, oligodendr
ocytes lining up their processes along axons, but not yet having start
ed to deposit a myelin sheath, were still MOG negative. However, in th
e same cultures, pseudo-myelinating oligodendrocytes (i.e., cells not
associated with neurites, but forming whorls of myelin-like figures) w
ere MOG positive. Similarly, rat CG4 cells, an oligodendrocyte-like ce
ll line, expressed MOG only after they had extended sheet-like process
es, which suggested that the activation of MOG transcription depends m
ore on an intrinsic oligodendroglial maturation program of myelination
than on a neuronal signal. (C) 1996 Wiley-Liss, Inc.