Olirdendrocytes assist in the maintenance of sodium channel clusters independent of the myelin sheath

Jeffrey L. Dupree*, Jeffrey L. Mason, Jill R. Marcus, Michael Stull, Rock Levinson, Glenn K. Matsushima, Brian Popko

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

47 Scopus citations


To ensure rapid and efficient impulse conduction, myelinated axons establish and maintain specific protein domains. For instance, sodium (Na+) channels accumulate in the node of Ranvier; potassium (K+) channels aggregate in the juxtaparanode and neurexin/caspr/paranodin clusters in the paranode. Our understanding of the mechanisms that control the initial clustering of these proteins is limited and less is known about domain maintenance. Correlative data indicate that myelin formation and/ or mature myelin-forming cells mediate formation of all three domains. Here, we test whether myelin is required for maintaining Na+ channel domains in the nodal gap by employing two demyelinating murine models: (1) cuprizone ingestion, which induces complete demyelination through oligodendrocyte toxicity; and (2) ceramide galactosyltransferase deficient mice, which undergo spontaneous adult-onset demyelination without oligodendrocyte death. Our data indicate that the myelin sheath is essential for long-term maintenance of sodium channel domains; however, oligodendrocytes, independent of myelin, provide a partial protective influence on the maintenance of nodal Na+ channel clusters. Thus, we propose that multiple mechanisms regulate the maintenance of nodal protein organization. Finally, we present evidence that following the loss of Na+ channel clusters the chronological progression of expression and reclustering of Na+ channel isoforms during the course of CNS remyelination recapitulates development.

Original languageEnglish (US)
Pages (from-to)179-192
Number of pages14
JournalNeuron Glia Biology
Issue number3
StatePublished - 2004


  • Protein domains
  • axolemma
  • demyelination
  • node of Ranvier

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology


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