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不同的自噬降解途径与神经退行性变。

The different autophagy degradation pathways and neurodegeneration.

机构信息

Department of Medical Genetics, University of Cambridge, Cambridge Institute for Medical Research, The Keith Peters Building, Cambridge Biomedical Campus, Hills Road, Cambridge CB2 0XY, UK; UK Dementia Research Institute, University of Cambridge, Cambridge Institute for Medical Research, The Keith Peters Building, Cambridge Biomedical Campus, Hills Road, Cambridge CB2 0XY, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.

Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France.

出版信息

Neuron. 2022 Mar 16;110(6):935-966. doi: 10.1016/j.neuron.2022.01.017. Epub 2022 Feb 7.

Abstract

The term autophagy encompasses different pathways that route cytoplasmic material to lysosomes for degradation and includes macroautophagy, chaperone-mediated autophagy, and microautophagy. Since these pathways are crucial for degradation of aggregate-prone proteins and dysfunctional organelles such as mitochondria, they help to maintain cellular homeostasis. As post-mitotic neurons cannot dilute unwanted protein and organelle accumulation by cell division, the nervous system is particularly dependent on autophagic pathways. This dependence may be a vulnerability as people age and these processes become less effective in the brain. Here, we will review how the different autophagic pathways may protect against neurodegeneration, giving examples of both polygenic and monogenic diseases. We have considered how autophagy may have roles in normal CNS functions and the relationships between these degradative pathways and different types of programmed cell death. Finally, we will provide an overview of recently described strategies for upregulating autophagic pathways for therapeutic purposes.

摘要

自噬涵盖了将细胞质物质运送到溶酶体进行降解的不同途径,包括巨自噬、伴侣介导的自噬和微自噬。由于这些途径对于降解聚集倾向的蛋白质和功能失调的细胞器(如线粒体)至关重要,因此它们有助于维持细胞内的平衡。由于有丝分裂后的神经元不能通过细胞分裂稀释不需要的蛋白质和细胞器积累,因此神经系统特别依赖于自噬途径。随着人们年龄的增长,这些过程在大脑中变得不那么有效,这种依赖性可能成为一种弱点。在这里,我们将回顾不同的自噬途径如何预防神经退行性变,并举例说明多基因和单基因疾病。我们已经考虑了自噬可能在中枢神经系统正常功能中发挥的作用,以及这些降解途径与不同类型的程序性细胞死亡之间的关系。最后,我们将概述最近描述的用于治疗目的上调自噬途径的策略。

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本文引用的文献

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Reciprocal regulation of chaperone-mediated autophagy and the circadian clock.伴侣蛋白介导的自噬与生物钟的相互调节。
Nat Cell Biol. 2021 Dec;23(12):1255-1270. doi: 10.1038/s41556-021-00800-z. Epub 2021 Dec 7.
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Vinexin contributes to autophagic decline in brain ageing across species.Vinexin 有助于跨物种的大脑衰老中的自噬下降。
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