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轴突-胶质细胞信号传导与轴突功能的胶质细胞支持

Axon-glial signaling and the glial support of axon function.

作者信息

Nave Klaus-Armin, Trapp Bruce D

机构信息

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, D-37075 Göttingen, Germany.

出版信息

Annu Rev Neurosci. 2008;31:535-61. doi: 10.1146/annurev.neuro.30.051606.094309.

Abstract

Oligodendrocytes and Schwann cells are highly specialized glial cells that wrap axons with a multilayered myelin membrane for rapid impulse conduction. Investigators have recently identified axonal signals that recruit myelin-forming Schwann cells from an alternate fate of simple axonal engulfment. This is the evolutionary oldest form of axon-glia interaction, and its function is unknown. Recent observations suggest that oligodendrocytes and Schwann cells not only myelinate axons but also maintain their long-term functional integrity. Mutations in the mouse reveal that axonal support by oligodendrocytes is independent of myelin assembly. The underlying mechanisms are still poorly understood; we do know that to maintain axonal integrity, mammalian myelin-forming cells require the expression of some glia-specific proteins, including CNP, PLP, and MAG, as well as intact peroxisomes, none of which is necessary for myelin assembly. Loss of glial support causes progressive axon degeneration and possibly local inflammation, both of which are likely to contribute to a variety of neuronal diseases in the central and peripheral nervous systems.

摘要

少突胶质细胞和施万细胞是高度特化的神经胶质细胞,它们用多层髓鞘膜包裹轴突,以实现快速冲动传导。研究人员最近发现了一些轴突信号,这些信号能使形成髓鞘的施万细胞从简单轴突吞噬的另一种命运中被招募过来。这是轴突与神经胶质细胞相互作用中进化上最古老的形式,其功能尚不清楚。最近的观察表明,少突胶质细胞和施万细胞不仅为轴突形成髓鞘,还维持其长期的功能完整性。小鼠身上的突变表明,少突胶质细胞对轴突的支持独立于髓鞘组装。其潜在机制仍知之甚少;我们确实知道,为了维持轴突的完整性,哺乳动物形成髓鞘的细胞需要表达一些神经胶质细胞特异性蛋白,包括2',3'-环核苷酸3'-磷酸二酯酶(CNP)、髓鞘脂蛋白(PLP)和髓鞘相关糖蛋白(MAG),以及完整的过氧化物酶体,而这些对于髓鞘组装都不是必需的。神经胶质细胞支持的丧失会导致轴突进行性退化,并可能引发局部炎症,这两者都可能导致中枢和周围神经系统中的多种神经元疾病。

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