Survival of, and competition between, oligodendrocytes expressing different alleles of thePlpgene
pmid: 12177040
pmc: PMC2174021
Survival of, and competition between, oligodendrocytes expressing different alleles of thePlpgene
Mutations in the X-linked Plp gene lead to dysmyelinating phenotypes and oligodendrocyte cell death. Here, we exploit the X inactivation phenomenon to show that a hierarchy exists in the influence of different mutant Plp alleles on oligodendrocyte survival. We used compound heterozygote mice to study the long-term fate of oligodendrocytes expressing either the jimpy or rumpshaker allele against a background of cells expressing a Plp-null allele. Although mutant and null oligodendrocytes were generated in equal numbers, the proportion expressing the mutant allele subsequently declined, but whereas those expressing the rumpshaker allele formed a reduced but stable population, the number of jimpy cells fell progressively. The age of decline in the jimpy cells in different regions of the CNS correlated with the temporal sequence of myelination. In compound heterozygotes expressing rumpshaker and jimpy alleles, oligodendrocytes expressing the former predominated and were more abundant than when the rumpshaker and null alleles were in competition. Thus, oligodendrocyte survival is not determined solely by cell intrinsic factors, such as the conformation of the misfolded PLP, but is influenced by neighboring cells, possibly competing for cell survival factors.
- Max Planck Society Germany
- University of Glasgow
- University of Glasgow United Kingdom
- University of Glasgow
- University of Glasgow
Central Nervous System, Protein Folding, Cell Death, Cell Survival, Cell Communication, Article, DNA-Binding Proteins, Mice, Oligodendroglia, Phenotype, Mutation, Animals, Alleles, Myelin Sheath, Transcription Factors
Central Nervous System, Protein Folding, Cell Death, Cell Survival, Cell Communication, Article, DNA-Binding Proteins, Mice, Oligodendroglia, Phenotype, Mutation, Animals, Alleles, Myelin Sheath, Transcription Factors
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