Department of Pathology, University of Pittsburgh School of Medicine, 200 Lothrop St., Rm. W958 BST, Pittsburgh, PA 15261, USA.
Neuropathol Appl Neurobiol. 2010 Apr;36(2):125-32. doi: 10.1111/j.1365-2990.2010.01062.x. Epub 2010 Feb 19.
Protein aggregation, mitochondrial impairment and oxidative stress are common to multiple neurodegenerative diseases. Homeostasis is regulated by a balanced set of anabolic and catabolic responses, which govern removal and repair of damaged proteins and organelles. Macroautophagy is an evolutionarily conserved pathway for the degradation of long-lived proteins, effete organelles and protein aggregates. Aberrations in macroautophagy have been observed in Alzheimer, Huntington, Parkinson, motor neuron and prion diseases. In this review, we will discuss the divergent roles of macroautophagy in neurodegenerative diseases and suggest a potential regulatory mechanism that could determine cell death or survival outcomes. We also highlight emerging data on neurite morphology and synaptic remodelling that indicate the possibility of detrimental functional trade-offs in the face of neuronal cell survival, particularly if the need for elevated macroautophagy is sustained.
蛋白质聚集、线粒体损伤和氧化应激是多种神经退行性疾病的共同特征。内稳态是通过一组平衡的合成代谢和分解代谢反应来调节的,这些反应控制着受损蛋白质和细胞器的清除和修复。巨自噬是一种用于降解长寿命蛋白质、失效细胞器和蛋白质聚集体的进化上保守的途径。在阿尔茨海默病、亨廷顿病、帕金森病、运动神经元病和朊病毒病中都观察到了巨自噬的异常。在这篇综述中,我们将讨论巨自噬在神经退行性疾病中的不同作用,并提出一种潜在的调节机制,该机制可能决定细胞死亡或存活的结果。我们还强调了关于神经突形态和突触重塑的新数据,这些数据表明,在神经元细胞存活的情况下,可能会产生有害的功能权衡,特别是如果需要持续提高巨自噬水平的话。