髓鞘
祖细胞
神经科学
多发性硬化
疾病
发病机制
白质营养不良
生物
脱髓鞘病
神经胶质
少突胶质细胞
神经学
免疫学
医学
干细胞
病理
中枢神经系统
细胞生物学
作者
Steven A. Goldman,Maiken Nedergaard,Martha S. Windrem
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-10-25
卷期号:338 (6106): 491-495
被引量:181
标识
DOI:10.1126/science.1218071
摘要
The diseases of myelin are among the most prevalent and disabling conditions in neurology. These diseases include both the vascular and inflammatory demyelinating disorders of adulthood, as well as the childhood leukodystrophies and cerebral palsy. These fundamentally glial disorders may be amenable to treatment by glial progenitor cells (GPCs), which give rise to astroglia and myelin-producing oligodendrocytes. Given the development of new methods for generating and isolating human GPCs, the myelin disorders may now be compelling targets for cell-based therapy. In addition, the efficient engraftment and expansion of human GPCs in murine hosts has led to the development of human glial chimeric mouse brains, which provides new opportunities for studying the species-specific roles of human glia in cognition, as well as in disease pathogenesis.
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