Doring Axinia, Yong Voon Wee
University of Calgary, Department of Clinical Neuroscience, Hotchkiss Brain Institute, Calgary, Canada.
Front Biosci (Schol Ed). 2011 Jun 1;3(3):846-56. doi: 10.2741/191.
A feature of most neurological disorders is demyelination, whereby myelin is lost from axons partly through stripping by macrophages/microglia. Spontaneous remyelination by oligodendrocytes that mature from oligodendrocyte precursor cells occurs following demyelination, even in the chronic inflammatory disorder of the central nervous system, multiple sclerosis. If remyelination does not occur or is prevented, then one consequence besides the loss of saltatory nerve conduction is the degeneration of axons. Thus, promoting remyelination is a desired result. In this article, we review the data that despite a reputation as "bad" factors for CNS wellbeing, including the promotion of neuroinflammation and demyelination, some aspects of macrophages/microglia activity are indeed "good", and can engender repair from the "ugly" phenomenon of demyelination. We discuss factors that help promote the benefits of macrophages/microglia activity for remyelination.
大多数神经系统疾病的一个特征是脱髓鞘,即髓磷脂部分通过巨噬细胞/小胶质细胞的剥离作用从轴突上丢失。即使在中枢神经系统的慢性炎症性疾病——多发性硬化症中,由少突胶质细胞前体细胞成熟而来的少突胶质细胞也会在脱髓鞘后自发进行髓鞘再生。如果髓鞘再生没有发生或受到阻碍,那么除了跳跃式神经传导丧失之外的一个后果就是轴突退化。因此,促进髓鞘再生是一个理想的结果。在本文中,我们回顾了相关数据,尽管巨噬细胞/小胶质细胞被认为是对中枢神经系统健康有“不良”影响的因素,包括促进神经炎症和脱髓鞘,但巨噬细胞/小胶质细胞活动的某些方面实际上是“有益的”,并且可以促使从脱髓鞘这种“不良”现象中修复。我们讨论了有助于促进巨噬细胞/小胶质细胞活动对髓鞘再生产生益处的因素。