Banerjee Swati, Bhat Manzoor A
Department of Cell and Molecular Physiology, Neurodevelopmental Disorders Research Center, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599-7545, USA.
J Neurosci Res. 2008 May 1;86(6):1189-98. doi: 10.1002/jnr.21574.
The ensheathment of neurons and their axons creates an ion-sensitive microenvironment that allows rapid conduction of nerve impulses. One of the fundamental questions about axonal ensheathment is how insulating glial cells wrap around axons. The mechanisms that underlie insulation of axons in invertebrates and vertebrates are not fully understood. In the present article we address cellular aspects of axonal ensheathment in Drosophila by taking advantage of glial mutants that illustrate a range of phenotypic defects including ensheathment of axons. From the findings of these mutant studies, we summarize that loss of glial cells, defects in glial membrane wrapping, failure of glial migration, and loss of specialized ladderlike septate junctions between ensheathing glial membranes result in axon-glial functional defects. These studies provide a broad perspective on glial ensheathment of axons in Drosophila and key insights into the anatomical and cellular aspects of axonal insulation. Given the powerful genetic approaches available in Drosophila, the axonal ensheathment process can be dissected in great detail to reveal the fundamental principles of ensheathment. These observations will be relevant to understanding the very similar processes in vertebrates, where defects in glial cell functions lead to devastating neurological diseases.
神经元及其轴突的被膜形成了一个离子敏感的微环境,使神经冲动能够快速传导。关于轴突被膜的一个基本问题是绝缘性胶质细胞如何围绕轴突。脊椎动物和无脊椎动物轴突绝缘的潜在机制尚未完全了解。在本文中,我们利用胶质突变体研究果蝇轴突被膜的细胞层面问题,这些突变体表现出一系列表型缺陷,包括轴突被膜异常。从这些突变体研究的结果中,我们总结出胶质细胞缺失、胶质细胞膜包裹缺陷、胶质细胞迁移失败以及包裹性胶质细胞膜之间特殊的梯状分隔连接缺失会导致轴突-胶质细胞功能缺陷。这些研究为果蝇轴突的胶质被膜提供了广阔的视角,并对轴突绝缘的解剖学和细胞层面提供了关键见解。鉴于果蝇中可用的强大遗传方法,可以非常详细地剖析轴突被膜过程,以揭示被膜的基本原理。这些观察结果将有助于理解脊椎动物中非常相似的过程,在脊椎动物中,胶质细胞功能缺陷会导致毁灭性的神经疾病。