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Molecular analysis of axonal-intrinsic and glial-associated co-regulation of axon degeneration

机译:轴突内在和神经胶质相关的轴突变性调控的分子分析

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摘要

Wallerian degeneration is an active program tightly associated with axonal degeneration, required for axonal regeneration and functional recovery after nerve damage. Here we provide a functional molecular foundation for our undertstanding of the complex non-cell autonomous role of glial cells in the regulation of axonal degeneration. To shed light on the complexity of the molecular machinery governing axonal degeneration we employ a multi-model, unbiased, in vivo approach combining morphological assesment and quantitative proteomics with in silico- based higher order functional clustering to genetically uncouple the intrinsic and extrinsic processes governing Wallerian degeneration. Highlighting a pivotal role for glial cells in the early stages fragmenting the axon by a cytokinesis-like process and a cell autonomous stage of axonal disintegration associated to mitochondrial dysfunction.
机译:Wallerian变性是与轴突变性紧密相关的活动程序,是神经损伤后轴突再生和功能恢复所必需的。在这里,我们为了解神经胶质细胞在轴突变性调控中的复杂的非细胞自主作用提供了功能性的分子基础。为了阐明控制轴突变性的分子机制的复杂性,我们采用了一种多模型,无偏见的体内方法,将形态学评估和定量蛋白质组学与基于计算机的高阶功能聚类相结合,从而遗传分离了控制Wallerian的内在和外在过程退化。突显了胶质细胞在早期通过与细胞线粒体功能障碍相关的胞质分裂样过程和轴突解体的细胞自主阶段使轴突断裂的关键作用。

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