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Drosophila Neuronal Injury Follows a Temporal Sequence of Cellular Events Leading to Degeneration at the Neuromuscular Junction

机译:果蝇神经元损伤遵循时间序列的细胞事件导致神经肌肉交界处的变性。

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摘要

Neurodegenerative diseases affect millions of people worldwide, and as the global population ages, there is a critical need to improve our understanding of the molecular and cellular mechanisms that drive neurodegeneration. At the molecular level, neurodegeneration involves the activation of complex signaling pathways that drive the active destruction of neurons and their intracellular components. Here, we use an in vivo motor neuron injury assay to acutely induce neurodegeneration in order to follow the temporal order of events that occur following injury in Drosophila melanogaster. We find that sites of injury can be rapidly identified based on structural defects to the neuronal cytoskeleton that result in disrupted axonal transport. Additionally, the neuromuscular junction accumulates ubiquitinated proteins prior to the neurodegenerative events, occurring at 24 hours post injury. Our data provide insights into the early molecular events that occur during axonal and neuromuscular degeneration in a genetically tractable model organism. Importantly, the mechanisms that mediate neurodegeneration in flies are conserved in humans. Thus, these studies have implications for our understanding of the cellular and molecular events that occur in humans and will facilitate the identification of biomedically relevant targets for future treatments.
机译:神经退行性疾病影响着全球数百万人,并且随着全球人口老龄化,迫切需要提高我们对驱动神经变性的分子和细胞机制的了解。在分子水平上,神经变性涉及激活神经元及其细胞内成分的主动破坏的复杂信号通路的激活。在这里,我们使用体内运动神经元损伤试验来急性诱导神经退行性病变,以遵循果蝇黑腹果蝇损伤后发生的事件的时间顺序。我们发现可以基于导致轴突运输受阻的神经元细胞骨架的结构缺陷快速确定损伤部位。另外,在损伤后24小时发生的神经退行性事件之前,神经肌肉接头会积聚遍在蛋白。我们的数据提供了对在遗传上易处理的模型生物中轴突和神经肌肉变性期间发生的早期分子事件的见解。重要的是,人类中介导果蝇神经变性的机制是保守的。因此,这些研究对我们理解人类中发生的细胞和分子事件具有重要意义,并将有助于确定生物医学相关靶标以用于未来治疗。

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