Mattedi Francesca, Vagnoni Alessio
Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, IoPPN, King's College London, London, United Kingdom.
Front Cell Neurosci. 2019 Aug 23;13:393. doi: 10.3389/fncel.2019.00393. eCollection 2019.
A fundamental question in cell biology is how cellular components are delivered to their destination with and precision within the crowded cytoplasmic environment. The long processes of neurons represent a significant challenge and make these cells particularly dependent on mechanisms for long-range cytoskeletal transport of proteins, RNA and organelles. Although many studies have substantiated a role for defective transport of axonal cargoes in the pathogenesis of neurodevelopmental and neurodegenerative diseases, remarkably little is known about how transport is regulated throughout ageing. The scale of the challenge posed by ageing is considerable because, in this case, the regulation of transport is ultimately dictated by the length of organismal lifespan, which can extend to days, years or decades. Recent methodological advances to study live axonal transport during ageing have provided new tools to scratch beneath the surface of this complex problem and revealed that age-dependent decline in the transport of mitochondria is a common feature across different neuronal populations of several model organisms. In certain instances, the molecular pathways that affect transport in ageing animals have begun to emerge. However, the functional implications of these observations are still not fully understood. Whether transport decline is a significant determinant of neuronal ageing or a mere consequence of decreased cellular fitness remains an open question. In this review, we discuss the latest developments in axonal trafficking in the ageing nervous system, along with the early studies that inaugurated this new area of research. We explore the possibility that the interplay between mitochondrial function and motility represents a crucial driver of ageing in neurons and put forward the hypothesis that declining axonal transport may be legitimately considered a hallmark of neuronal ageing.
细胞生物学中的一个基本问题是,在拥挤的细胞质环境中,细胞成分如何精确无误地被运送到它们的目的地。神经元长长的轴突带来了巨大的挑战,使得这些细胞特别依赖于蛋白质、RNA和细胞器的长距离细胞骨架运输机制。尽管许多研究证实了轴突货物运输缺陷在神经发育和神经退行性疾病发病机制中的作用,但对于衰老过程中运输是如何被调控的,我们却知之甚少。衰老带来的挑战规模相当大,因为在这种情况下,运输的调控最终取决于生物体的寿命长度,而生物体寿命可以延长至数天、数年或数十年。最近在研究衰老过程中轴突实时运输方面的方法进展提供了新工具,使我们能够深入探究这个复杂问题的表面之下,并揭示出线粒体运输的年龄依赖性下降是几种模式生物不同神经元群体中的一个共同特征。在某些情况下,影响衰老动物运输的分子途径已经开始显现。然而,这些观察结果的功能意义仍未完全被理解。运输能力下降是神经元衰老的一个重要决定因素,还是仅仅是细胞适应性降低的结果,这仍然是一个悬而未决的问题。在这篇综述中,我们讨论了衰老神经系统中轴突运输的最新进展,以及开创这一研究新领域的早期研究。我们探讨了线粒体功能和运动性之间的相互作用可能是神经元衰老的关键驱动因素这一可能性,并提出轴突运输能力下降可以被合理地视为神经元衰老的一个标志这一假设。