Autophagy in ageing and ageing-related neurodegenerative diseases

C. Karabiyik, Rebecca A. Frake, So Jung Park, Mariana Pavel, D. Rubinsztein
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引用次数: 15

Abstract

Autophagy is a catabolic mechanism that allows cells to deliver cytoplasmic contents to lysosomes for degradation to maintain energy homeostasis and to protect cells against stress. Autophagy has been directly linked to neurodegeneration and ageing by an extensive body of research. It has become evident that disruption of autophagy contributes significantly to age-related pathologies and to the cognitive and motor declines associated with “healthy” ageing. Autophagic dysfunction causes the accumulation of many of the toxic, aggregate-prone proteins that are responsible for neurodegenerative diseases, including mutant huntingtin, alpha-synuclein, tau, and others. Since upregulation of autophagy has been found to reduce levels of such protein species, the therapeutic potential of autophagy induction as a strategy against age-related diseases and a method for modulating longevity has been widely studied. Here we review the evidence supporting a role for autophagy dysfunction in the progression of the age-associated functional decline in the brain and age-related brain pathologies and discuss the available evidence that upregulation of autophagy may be a valuable therapeutic strategy.
衰老和衰老相关神经退行性疾病中的自噬
自噬是一种分解代谢机制,它允许细胞将细胞质内容物传递给溶酶体进行降解,以维持能量稳态并保护细胞免受应激。大量研究表明,自噬与神经退行性变和衰老直接相关。很明显,自噬的破坏在很大程度上导致了与年龄相关的病理以及与“健康”衰老相关的认知和运动能力下降。自噬功能障碍导致许多有毒的、易聚集的蛋白质的积累,这些蛋白质是导致神经退行性疾病的原因,包括突变的亨廷顿蛋白、α -突触核蛋白、tau蛋白等。由于自噬的上调已被发现可降低这类蛋白的水平,自噬诱导作为对抗年龄相关疾病的策略和调节寿命的方法的治疗潜力已被广泛研究。在这里,我们回顾了支持自噬功能障碍在脑年龄相关功能衰退和年龄相关脑病理进展中的作用的证据,并讨论了上调自噬可能是一种有价值的治疗策略的现有证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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