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Chronic oligodendrocyte injury in central nervous system pathologies

期刊

COMMUNICATIONS BIOLOGY
卷 5, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s42003-022-04248-1

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资金

  1. Medical Research Council Senior Non-Clinical Fellowship
  2. United Kingdom Dementia Research Institute at The University of Edinburgh
  3. Astex Pharmaceuticals
  4. John David Eaton Chair in Multiple Sclerosis Research at the Barlo Multiple Sclerosis Centre
  5. Progressive MS Alliance MSIF

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This Perspective discusses the contribution of oligodendrocyte injury to neurological disease and the potential for therapeutic targeting. Targeting mature oligodendrocyte health is proposed as a promising therapeutic strategy to support central nervous system function.
In this Perspective, Molina-Gonzalez and co-authors discuss the contribution of oligodendrocyte injury to neurological disease and the potential for their therapeutic targeting. Myelin, the membrane surrounding neuronal axons, is critical for central nervous system (CNS) function. Injury to myelin-forming oligodendrocytes (OL) in chronic neurological diseases (e.g. multiple sclerosis) ranges from sublethal to lethal, leading to OL dysfunction and myelin pathology, and consequent deleterious impacts on axonal health that drive clinical impairments. This is regulated by intrinsic factors such as heterogeneity and age, and extrinsic cellular and molecular interactions. Here, we discuss the responses of OLs to injury, and perspectives for therapeutic targeting. We put forward that targeting mature OL health in neurological disease is a promising therapeutic strategy to support CNS function.

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