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Spatiotemporal Control of CNS Myelination by Oligodendrocyte Programmed Cell Death through the TFEB-PUMA Axis.
Sun, Lu O; Mulinyawe, Sara B; Collins, Hannah Y; Ibrahim, Adiljan; Li, Qingyun; Simon, David J; Tessier-Lavigne, Marc; Barres, Ben A.
Afiliação
  • Sun LO; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: lsun2@stanford.edu.
  • Mulinyawe SB; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Collins HY; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Ibrahim A; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Li Q; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Simon DJ; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Tessier-Lavigne M; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Barres BA; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Cell ; 175(7): 1811-1826.e21, 2018 12 13.
Article em En | MEDLINE | ID: mdl-30503207
ABSTRACT
Nervous system function depends on proper myelination for insulation and critical trophic support for axons. Myelination is tightly regulated spatially and temporally, but how it is controlled molecularly remains largely unknown. Here, we identified key molecular mechanisms governing the regional and temporal specificity of CNS myelination. We show that transcription factor EB (TFEB) is highly expressed by differentiating oligodendrocytes and that its loss causes precocious and ectopic myelination in many parts of the murine brain. TFEB functions cell-autonomously through PUMA induction and Bax-Bak activation to promote programmed cell death of a subset of premyelinating oligodendrocytes, allowing selective elimination of oligodendrocytes in normally unmyelinated brain regions. This pathway is conserved across diverse brain areas and is critical for myelination timing. Our findings define an oligodendrocyte-intrinsic mechanism underlying the spatiotemporal specificity of CNS myelination, shedding light on how myelinating glia sculpt the nervous system during development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Oligodendroglia / Neuroglia / Apoptose / Proteínas Supressoras de Tumor / Proteínas Reguladoras de Apoptose / Fatores de Transcrição de Zíper de Leucina e Hélice-Alça-Hélix Básicos / Bainha de Mielina Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Oligodendroglia / Neuroglia / Apoptose / Proteínas Supressoras de Tumor / Proteínas Reguladoras de Apoptose / Fatores de Transcrição de Zíper de Leucina e Hélice-Alça-Hélix Básicos / Bainha de Mielina Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article