TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice - Aix-Marseille Université Accéder directement au contenu
Article Dans Une Revue Nature Communications Année : 2023

TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice

Résumé

The mechanisms regulating myelin repair in the adult central nervous system (CNS) are unclear. Here, we identify DNA hydroxymethylation, catalyzed by the Ten-Eleven-Translocation (TET) enzyme TET1, as necessary for myelin repair in young adults and defective in old mice. Constitutive and inducible oligodendrocyte lineage-specific ablation of Tet1 (but not of Tet2 ), recapitulate this age-related decline in repair of demyelinated lesions. DNA hydroxymethylation and transcriptomic analyses identify TET1-target in adult oligodendrocytes, as genes regulating neuro-glial communication, including the solute carrier ( Slc ) gene family. Among them, we show that the expression levels of the Na + /K + /Cl − transporter, SLC12A2, are higher in Tet1 overexpressing cells and lower in old or Tet1 knockout. Both aged mice and Tet1 mutants also present inefficient myelin repair and axo-myelinic swellings. Zebrafish mutants for slc12a2b also display swellings of CNS myelinated axons. Our findings suggest that TET1 is required for adult myelin repair and regulation of the axon-myelin interface.
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hal-04146392 , version 1 (30-06-2023)

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Sarah Moyon, Rebecca Frawley, Damien Marechal, Dennis Huang, Katy L H Marshall-Phelps, et al.. TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice. Nature Communications, 2023, 12 (1), pp.3359. ⟨10.1038/s41467-021-23735-3⟩. ⟨hal-04146392⟩

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