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大脑衰老和阿尔茨海默病中自噬和线粒体自噬受损。

Compromised autophagy and mitophagy in brain ageing and Alzheimer's diseases.

作者信息

Caponio Domenica, Veverová Kateřina, Zhang Shi-Qi, Shi Liu, Wong Garry, Vyhnalek Martin, Fang Evandro F

机构信息

Department of Clinical Molecular Biology, University of Oslo and Akershus University Hospital, 1478 Lørenskog, Norway.

Memory Clinic, Department of Neurology, Charles University, 2nd Faculty of Medicine and Motol University Hospital, Prague, Czech Republic.

出版信息

Aging Brain. 2022 Nov 24;2:100056. doi: 10.1016/j.nbas.2022.100056. eCollection 2022.

Abstract

Alzheimer's disease (AD) is one of the most persistent and devastating neurodegenerative disorders of old age, and is characterized clinically by an insidious onset and a gradual, progressive deterioration of cognitive abilities, ranging from loss of memory to impairment of judgement and reasoning. Despite years of research, an effective cure is still not available. Autophagy is the cellular 'garbage' clearance system which plays fundamental roles in neurogenesis, neuronal development and activity, and brain health, including memory and learning. A selective sub-type of autophagy is mitophagy which recognizes and degrades damaged or superfluous mitochondria to maintain a healthy and necessary cellular mitochondrial pool. However, emerging evidence from animal models and human samples suggests an age-dependent reduction of autophagy and mitophagy, which are also compromised in AD. Upregulation of autophagy/mitophagy slows down memory loss and ameliorates clinical features in animal models of AD. In this review, we give an overview of autophagy and mitophagy and their link to the progression of AD. We also summarize approaches to upregulate autophagy/mitophagy. We hypothesize that age-dependent compromised autophagy/mitophagy is a cause of brain ageing and a risk factor for AD, while restoration of autophagy/mitophagy to more youthful levels could return the brain to health.

摘要

阿尔茨海默病(AD)是老年期最持久且最具破坏性的神经退行性疾病之一,其临床特征为隐匿起病,认知能力从记忆丧失到判断和推理受损逐渐进行性恶化。尽管经过多年研究,仍未找到有效的治愈方法。自噬是细胞的“垃圾”清除系统,在神经发生、神经元发育与活动以及脑健康(包括记忆和学习)中发挥着重要作用。自噬的一种选择性亚型是线粒体自噬,它识别并降解受损或多余的线粒体,以维持健康且必要的细胞线粒体库。然而,来自动物模型和人类样本的新证据表明,自噬和线粒体自噬会随年龄增长而减少,在AD中也会受到损害。在AD动物模型中,自噬/线粒体自噬的上调可减缓记忆丧失并改善临床特征。在本综述中,我们概述了自噬和线粒体自噬及其与AD进展的联系。我们还总结了上调自噬/线粒体自噬的方法。我们推测,年龄依赖性的自噬/线粒体自噬受损是脑衰老的原因和AD的危险因素,而将自噬/线粒体自噬恢复到更年轻的水平可能使大脑恢复健康。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8421/9997167/5950f9ac59c2/gr1.jpg

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