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Mechanisms of injury-induced axon degeneration

机译:伤害诱导的轴突变性机制

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Injury-induced axon degeneration in model organisms and cell culture has emerged as an area of growing interest due to its experimental tractability and to the promise of identifying conserved mechanisms that mediate axon loss in human disease. Injury-induced axon degeneration is also observed within the well-studied process of Wallerian degeneration, a complex phenomenon triggered by axon injury to peripheral nerves in mammals. Recent studies have led to the identification of key molecular components of injury-induced axon degeneration. Axon survival factors, such as NMNAT2, act to protect injured axons from degeneration. By contrast, factors such as SARM1, MAPK, and PHR1 act to promote degeneration. The coordinated activity of these factors determines axon fate after injury. Since axon loss is an early feature of neurodegenerative diseases, it is possible that understanding the molecular mechanism of injury-induced degeneration will lead to new treatments for axon loss in neurodegenerative disease. Here, we discuss the critical pathways for injury-induced axon degeneration across species with an emphasis on their interactions in an integrated signaling network.
机译:模型生物和细胞培养中的伤害诱导的轴突变性由于其实验途径和识别官方疾病中轴突丧失的保守机制的承诺而出现了越来越感兴趣的领域。在Wallerian变性的良好研究过程中也观察到损伤诱导的轴突变性,这是由轴颈损伤引发的复杂现象对哺乳动物的外周神经引发。最近的研究导致鉴定损伤轴突变性的关键分子组分。轴突存活因子,如NMNAT2,采取免受退化保护受伤的轴突。相比之下,诸如SARM1,MAPK和PHR1等因素,以促进退化。这些因素的协调活动决定了伤害后的轴突命运。由于轴突损失是神经变性疾病的早期特征,因此理解损伤的损伤的分子机制可能导致神经变性疾病中的轴突损失的新治疗方法。在这里,我们讨论了跨越物种伤害引起的轴突变性的关键途径,重点是它们在集成信令网络中的相互作用。

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