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SOX6 Identified as Molecular Brake on Myelin Repair in MS, Mouse Study Shows Rapid Remyelination

The paper presents SOX6 inhibition as a potential strategy to restart myelin repair in patients.

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Overview

  • Case Western Reserve University's Institute for Glial Sciences reports the findings in Cell on August 25, identifying SOX6 as a key regulator that times oligodendrocyte maturation.
  • The team describes a mechanism they call gene melting through which SOX6 keeps oligodendrocytes in an immature state during normal development.
  • Analysis of human brain data shows an overabundance of SOX6-linked immature oligodendrocytes in multiple sclerosis samples, a pattern not seen in Alzheimer’s or Parkinson’s cohorts examined.
  • Reducing SOX6 with an antisense oligonucleotide in mouse models drove rapid oligodendrocyte maturation and local myelination within days.
  • The work establishes preclinical proof-of-concept and will require further mechanistic study, safety evaluation, and CNS delivery optimization before human testing.