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• W2023942293 abstract "New CNS neurons and glia are generated throughout adulthood from endogenous neural stem and progenitor cells. These progenitors can respond to injury, but their ability to proliferate, migrate, differentiate, and survive is usually insufficient to replace lost cells and restore normal function. Potentiating the progenitor response with exogenous factors is an attractive strategy for the treatment of nervous system injuries and neurodegenerative and demyelinating disorders. Previously, we reported that delivery of leukemia inhibitory factor (LIF) to the CNS stimulates the self-renewal of neural stem cells and the proliferation of parenchymal glial progenitors. Here we identify these parenchymal glia as oligodendrocyte (OL) progenitor cells (OPCs) and show that LIF delivery stimulates their proliferation through the activation of gp130 receptor signaling within these cells. Importantly, this effect of LIF on OPC proliferation can be harnessed to enhance the generation of OLs that express myelin proteins and reform nodes of Ranvier in the context of chronic demyelination in the adult mouse hippocampus. Our findings, considered together with the known beneficial effects of LIF on OL and neuron survival, suggest that LIF has both reparative and protective activities that make it a promising potential therapy for CNS demyelinating disorders and injuries." @default.
• W2023942293 created "2016-06-24" @default.
• W2023942293 creator A5003624509 @default.
• W2023942293 creator A5014515859 @default.
• W2023942293 date "2012-02-08" @default.
• W2023942293 modified "2023-10-13" @default.
• W2023942293 title "Exogenous Leukemia Inhibitory Factor Stimulates Oligodendrocyte Progenitor Cell Proliferation and Enhances Hippocampal Remyelination" @default.
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• W2023942293 doi "https://doi.org/10.1523/jneurosci.3803-11.2012" @default.
• W2023942293 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3561904" @default.
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