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胶质细胞对轴突完整性的髓鞘形成和支持。

Myelination and support of axonal integrity by glia.

机构信息

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Hermann-Rein-Strasse 3, 37075 Göttingen, Germany.

出版信息

Nature. 2010 Nov 11;468(7321):244-52. doi: 10.1038/nature09614.

Abstract

The myelination of axons by glial cells was the last major step in the evolution of cells in the vertebrate nervous system, and white-matter tracts are key to the architecture of the mammalian brain. Cell biology and mouse genetics have provided insight into axon-glia signalling and the molecular architecture of the myelin sheath. Glial cells that myelinate axons were found to have a dual role by also supporting the long-term integrity of those axons. This function may be independent of myelin itself. Myelin abnormalities cause a number of neurological diseases, and may also contribute to complex neuropsychiatric disorders.

摘要

少突胶质细胞对轴突的髓鞘化是脊椎动物神经系统细胞进化的最后一个主要步骤,而白质束是哺乳动物大脑结构的关键。细胞生物学和小鼠遗传学为轴突-胶质细胞信号转导和髓鞘的分子结构提供了深入了解。研究发现,对轴突进行髓鞘化的神经胶质细胞具有双重作用,既能支持这些轴突的长期完整性,也能支持这些轴突的长期完整性。这一功能可能与髓鞘本身无关。髓鞘异常会导致多种神经疾病,也可能导致复杂的神经精神疾病。

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