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恢复神经退行性疾病中自噬和溶酶体功能的分子靶点和方法。

Molecular targets and approaches to restore autophagy and lysosomal capacity in neurodegenerative disorders.

机构信息

Novartis Institutes for BioMedical Research, Basel, Switzerland.

Novartis Institutes for BioMedical Research, Cambridge, MA, USA.

出版信息

Mol Aspects Med. 2021 Dec;82:101018. doi: 10.1016/j.mam.2021.101018. Epub 2021 Sep 4.

Abstract

Autophagy is a catabolic process that promotes cellular fitness by clearing aggregated protein species, pathogens and damaged organelles through lysosomal degradation. The autophagic process is particularly important in the nervous system where post-mitotic neurons rely heavily on protein and organelle quality control in order to maintain cellular health throughout the lifetime of the organism. Alterations of autophagy and lysosomal function are hallmarks of various neurodegenerative disorders. In this review, we conceptualize some of the mechanistic and genetic evidence pointing towards autophagy and lysosomal dysfunction as a causal driver of neurodegeneration. Furthermore, we discuss rate-limiting pathway nodes and potential approaches to restore pathway activity, from autophagy initiation, cargo sequestration to lysosomal capacity.

摘要

自噬是一种分解代谢过程,通过溶酶体降解清除聚集的蛋白质种类、病原体和受损的细胞器,从而促进细胞健康。自噬过程在神经系统中尤为重要,因为有丝分裂后的神经元在整个生物体的生命周期中严重依赖于蛋白质和细胞器的质量控制来维持细胞健康。自噬和溶酶体功能的改变是各种神经退行性疾病的标志。在这篇综述中,我们将一些指向自噬和溶酶体功能障碍作为神经退行性变的因果驱动因素的机制和遗传证据概念化。此外,我们还讨论了限速途径节点和恢复途径活性的潜在方法,从自噬起始、货物隔离到溶酶体容量。

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