Departments of Oncology and Clinical Neuroscience, University of Calgary, Alberta, Canada.
Glia. 2018 Sep;66(9):1809-1825. doi: 10.1002/glia.23333. Epub 2018 Mar 30.
The repair of myelin, termed remyelination, is a regenerative process that occurs within the central nervous system in conditions such as multiple sclerosis. Remyelination is enabled by oligodendrocytes that mature from oligodendrocyte precursor cells. Many factors influence the biology of oligodendrocytes and their capacity to reform myelin, and considerable evidence now implicates the extracellular matrix within the injured central nervous system as a major modifier of remyelination. Herein, we review current knowledge of components of the brain extracellular matrix that are beneficial or inhibitory for oligodendrocyte recruitment and maturation, and for their capacity to remyelinate where evidence exists. We highlight the detrimental roles of the chondroitin sulfate proteoglycans in remyelination and discuss approaches to alter the brain extracellular matrix for the wellbeing of oligodendrocytes and their capacity for myelin regeneration.
髓鞘的修复,称为髓鞘再生,是中枢神经系统中在多发性硬化等情况下发生的一种再生过程。髓鞘再生是由从少突胶质前体细胞成熟而来的少突胶质细胞所实现的。许多因素影响少突胶质细胞的生物学特性及其形成髓鞘的能力,现在有大量证据表明,损伤的中枢神经系统中的细胞外基质是调节髓鞘再生的主要因素。本文综述了目前对大脑细胞外基质成分的认识,这些成分对少突胶质细胞的募集和成熟以及在有证据的情况下它们的髓鞘再生能力有有益或抑制作用。我们强调了软骨素硫酸盐蛋白聚糖在髓鞘再生中的有害作用,并讨论了改变大脑细胞外基质以促进少突胶质细胞及其髓鞘再生能力的方法。