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Myelin/oligodendrocyte glycoprotein (MOG) expression is associated with myelin deposition
S K Solly1, J L Thomas, M Monge
1Laboratoire de Neurobiologie Cellulaire, Moléculaire, et Clinique INSERM U-134, Hôpital de la Salpêtrière, Université Pierre et Marie Curie, Paris, France.
Abstract:
We investigated the onset of expression of the myelin/oligodendrocyte glycoprotein (MOG) mRNA and protein in the developing mouse central nervous system. In situ hybridization on brain sections at different stages of embryonic and postnatal development showed that MOG transcripts were first detected at birth in the medulla oblongata. During the first week after birth, cells expressing MOG mRNA were located in the ventral longitudinal funiculus. During the second postnatal week, the pattern of MOG mRNA expression extended rostrally to the mid-forebrain regions and reached completion by the beginning of the third week. MOG transcription was delayed by several days with respect to myelin basic protein (MBP), and it appeared that while the MBP probe labeled both non-myelinating and myelinating oligodendrocytes, only the latter were MOG-positive. In vitro, immunocytochemical analysis of MOG protein expression, performed on myelinating cultures derived from mouse brain embryos at 15 days of gestation, confirmed the strict restriction of MOG expression to myelinating oligodendrocytes. In particular, oligodendrocytes lining up their processes along axons, but not yet having started to deposit a myelin sheath, were still MOG negative. However, in the same cultures, pseudo-myelinating oligodendrocytes (i.e., cells not associated with neurites, but forming whorls of myelin-like figures) were MOG positive. Similarly, rat CG4 cells, an oligodendrocyte-like cell line, expressed MOG only after they had extended sheet-like processes, which suggested that the activation of MOG transcription depends more on an intrinsic oligodendroglial maturation program of myelination than on a neuronal signal.
Insights
Myelin/oligodendrocyte glycoprotein (MOG) expression begins at birth in mouse brains, specifically in myelinating oligodendrocytes. MOG is not expressed until myelination is initiated, indicating an intrinsic maturation program.
Area of Science:
- Neuroscience
- Developmental Biology
- Cell Biology
Background:
- The myelin/oligodendrocyte glycoprotein (MOG) is a crucial component of the myelin sheath in the central nervous system.
- Understanding the precise timing and regulation of MOG expression is vital for comprehending oligodendrocyte development and myelination processes.
Purpose of the Study:
- To investigate the temporal and spatial onset of myelin/oligodendrocyte glycoprotein (MOG) mRNA and protein expression during the development of the mouse central nervous system.
- To determine the relationship between MOG expression and the myelination status of oligodendrocytes.
Main Methods:
- In situ hybridization was employed to detect MOG mRNA expression in developing mouse brain sections at various embryonic and postnatal stages.
- Immunocytochemical analysis was performed on in vitro myelinating cultures and rat CG4 oligodendrocyte-like cell lines to assess MOG protein expression.
Main Results:
- MOG transcripts were first detected at birth in the medulla oblongata, with expression patterns expanding rostrally over the first three postnatal weeks.
- MOG expression was strictly restricted to myelinating oligodendrocytes, distinguishing them from non-myelinating or pre-myelinating cells.
- MOG expression in cell cultures was initiated only after the extension of sheet-like processes, suggesting an intrinsic program for myelination.
Conclusions:
- MOG expression is a late event in oligodendrocyte differentiation, specifically linked to the active myelination process.
- The onset of MOG transcription appears to be driven by an intrinsic oligodendroglial maturation program rather than solely by neuronal signals.