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Axonal Transport Phase-Separated Compartments and Neuron Mechanics - A New Approach to Investigate Neurodegenerative Diseases

机译:轴突运输相分隔室和神经元力学-研究神经退行性疾病的新方法

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摘要

Many molecular and cellular pathogenic mechanisms of neurodegenerative diseases have been revealed. However, it is unclear what role a putatively impaired neuronal transport with respect to altered mechanical properties of neurons play in the initiation and progression of such diseases. The biochemical aspects of intracellular axonal transport, which is important for molecular movements through the cytoplasm, e.g., mitochondrial movement, has already been studied. Interestingly, transport deficiencies are associated with the emergence of the affliction and potentially linked to disease transmission. Transport along the axon depends on the normal function of the neuronal cytoskeleton, which is also a major contributor to neuronal mechanical properties. By contrast, little attention has been paid to the mechanical properties of neurons and axons impaired by neurodegeneration, and of membraneless, phase-separated organelles such as stress granules (SGs) within neurons. Mechanical changes may indicate cytoskeleton reorganization and function, and thus give information about the transport and other system impairment. Nowadays, several techniques to investigate cellular mechanical properties are available. In this review, we discuss how select biophysical methods to probe material properties could contribute to the general understanding of mechanisms underlying neurodegenerative diseases.
机译:已经揭示了神经退行性疾病的许多分子和细胞致病机制。但是,尚不清楚假定的受损的神经元运输相对于神经元机械特性的改变在此类疾病的发生和发展中起什么作用。已经研究了细胞内轴突运输的生化方面,这对于通过细胞质的分子运动例如线粒体运动很重要。有趣的是,运输缺陷与疾病的发生有关,并可能与疾病传播有关。沿着轴突的运输取决于神经元细胞骨架的正常功能,这也是神经元机械特性的主要贡献者。相比之下,很少关注神经变性引起的神经元和轴突的机械性质,以及神经元内无膜,相分离的细胞器(如应激颗粒(SGs​​))的机械性质。机械变化可能表明细胞骨架的重组和功能,从而提供有关转运和其他系统损伤的信息。如今,可以使用几种研究细胞力学性能的技术。在这篇综述中,我们讨论了选择生物物理方法来探测物质特性如何有助于对神经退行性疾病的潜在机制的一般理解。

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