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Pushing Forward: Remyelination as the New Frontier in CNS Diseases

Journal

TRENDS IN NEUROSCIENCES
Volume 39, Issue 4, Pages 246-263

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tins.2016.02.004

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Funding

  1. German Research Council (DFG) [SPP1757, KU1934/5-1]
  2. Christiane and Claudia Hempel Foundation
  3. AFM (Association Francaise contre les Myopathies)
  4. Wafter and Ilse Rose Foundation
  5. James and Elisabeth Cloppenburg, Peek & Cloppenburg Dusseldorf Foundation

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The evolutionary acquisition of myelin sheaths around large caliber axons in the central nervous system (CNS) represented a milestone in the development of vertebrate higher brain function. Myelin ensheathment of axons enabled saltatory conduction and thus accelerated information processing. However, a number of CNS diseases harm or destroy myelin and oligodendrocytes (myelin -producing cells), ultimately resulting in demyelination. In the adult CNS, new oligodendrocytes can be generated from a quiescent pool of precursor cells, which-upon differentiation-can replace lost myelin sheaths. The efficiency of this spontaneous regeneration is limited, which leads to incomplete remyelination and residual clinical symptoms. Here, we discuss CNS pathologies characterized by white matter degeneration and regeneration and highlight drugs that could potentially serve as remyelination therapies.

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