Glia Disease and Repair - Remyelination

被引:151
作者
Franklin, Robin J. M. [1 ]
Goldman, Steven A. [2 ,3 ]
机构
[1] Univ Cambridge, Wellcome Trust Med Res Council Cambridge Stem Cel, Cambridge CB3 0ES, England
[2] Univ Rochester, Med Ctr, Ctr Translat Neuromed, Rochester, NY 14642 USA
[3] Univ Copenhagen, Fac Med, DK-2200 Copenhagen, Denmark
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2015年 / 7卷 / 07期
关键词
CENTRAL-NERVOUS-SYSTEM; OLIGODENDROCYTE PROGENITOR CELLS; FIBRILLARY ACIDIC PROTEIN; MULTIPLE-SCLEROSIS LESIONS; SUBCORTICAL WHITE-MATTER; INCREASING LOCAL-LEVELS; PLURIPOTENT STEM-CELLS; SPINAL-CORD; CNS REMYELINATION; SCHWANN-CELL;
D O I
10.1101/cshperspect.a020594
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The inability of the mammalian central nervous system (CNS) to undergo spontaneous regeneration has long been regarded as a central tenet of neurobiology. However, although this is largely true of the neuronal elements of the adult mammalian CNS, save for discrete populations of granular neurons, the same is not true of its glial elements. In particular, the loss of oligodendrocytes, which results in demyelination, triggers a spontaneous and often highly efficient regenerative response, remyelination, in which new oligodendrocytes are generated andmyelin sheaths are restored to denuded axons. Yet, remyelination in humans is not without limitation, and a variety of demyelinating conditions are associated with sustained and disabling myelin loss. In this review, we will review the biology of remyelination, including the cells and signals involved; describewhen remyelination occurs and when and why it fails and the consequences of its failure; and discuss approaches for therapeutically enhancing remyelination in demyelinating diseases of both children and adults, both by stimulating endogenous oligodendrocyte progenitor cells and by transplanting these cells into demyelinated brain.
引用
收藏
页码:1 / 28
页数:28
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