| Literature DB >> 21131950 |
Jeffrey K Huang1, Andrew A Jarjour2, Brahim Nait Oumesmar3, Christophe Kerninon3, Anna Williams2, Wojciech Krezel4, Hiroyuki Kagechika5, Julien Bauer6, Chao Zhao1, Anne Baron-Van Evercooren3, Pierre Chambon4, Charles Ffrench-Constant2, Robin J M Franklin1.
Abstract
The molecular basis of CNS myelin regeneration (remyelination) is poorly understood. We generated a comprehensive transcriptional profile of the separate stages of spontaneous remyelination that follow focal demyelination in the rat CNS and found that transcripts that encode the retinoid acid receptor RXR-γ were differentially expressed during remyelination. Cells of the oligodendrocyte lineage expressed RXR-γ in rat tissues that were undergoing remyelination and in active and remyelinated multiple sclerosis lesions. Knockdown of RXR-γ by RNA interference or RXR-specific antagonists severely inhibited oligodendrocyte differentiation in culture. In mice that lacked RXR-γ, adult oligodendrocyte precursor cells efficiently repopulated lesions after demyelination, but showed delayed differentiation into mature oligodendrocytes. Administration of the RXR agonist 9-cis-retinoic acid to demyelinated cerebellar slice cultures and to aged rats after demyelination caused an increase in remyelinated axons. Our results indicate that RXR-γ is a positive regulator of endogenous oligodendrocyte precursor cell differentiation and remyelination and might be a pharmacological target for regenerative therapy in the CNS.Entities:
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Year: 2010 PMID: 21131950 PMCID: PMC4013508 DOI: 10.1038/nn.2702
Source DB: PubMed Journal: Nat Neurosci ISSN: 1097-6256 Impact factor: 24.884