Sakurai Maria, Kuwahara Tomoki
Department of Neuropathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Front Cell Dev Biol. 2025 Jan 30;13:1518991. doi: 10.3389/fcell.2025.1518991. eCollection 2025.
Autophagy is the major degradation process in cells and is involved in a variety of physiological and pathological functions. While macroautophagy, which employs a series of molecular cascades to form ATG8-coated double membrane autophagosomes for degradation, remains the well-known type of canonical autophagy, microautophagy and chaperon-mediated autophagy have also been characterized. On the other hand, recent studies have focused on the functions of autophagy proteins beyond intracellular degradation, including noncanonical autophagy, also known as the conjugation of ATG8 to single membranes (CASM), and autophagy-related extracellular secretion. In particular, CASM is unique in that it does not require autophagy upstream mechanisms, while the ATG8 conjugation system is involved in a manner different from canonical autophagy. There have been many reports on the involvement of these autophagy-related mechanisms in neurodegenerative diseases, with Parkinson's disease (PD) receiving particular attention because of the important roles of several causative and risk genes, including LRRK2. In this review, we will summarize and discuss the contributions of canonical and noncanonical autophagy to cellular functions, with a special focus on the pathogenesis of PD.
自噬是细胞内主要的降解过程,参与多种生理和病理功能。虽然巨自噬利用一系列分子级联反应形成包裹有ATG8的双膜自噬体进行降解,仍然是经典自噬中广为人知的类型,但微自噬和伴侣介导的自噬也已得到表征。另一方面,最近的研究集中在自噬蛋白在细胞内降解之外的功能,包括非经典自噬,也称为ATG8与单膜的结合(CASM),以及与自噬相关的细胞外分泌。特别是,CASM的独特之处在于它不需要自噬上游机制,而ATG8结合系统以不同于经典自噬的方式参与其中。关于这些自噬相关机制参与神经退行性疾病的报道很多,帕金森病(PD)由于包括LRRK2在内的几个致病和风险基因的重要作用而受到特别关注。在这篇综述中,我们将总结和讨论经典和非经典自噬对细胞功能的贡献,特别关注PD的发病机制。