最初由 HOPS 介导的融合事件对于从轴突末端开始的自噬体运输至关重要。

Autophagy Pub Date : 2024-10-01 Epub Date: 2024-06-20 DOI:10.1080/15548627.2024.2366122
Serena R Wisner, Madison Chlebowski, Amrita Mandal, Don Mai, Chris Stein, Ronald S Petralia, Ya-Xian Wang, Catherine M Drerup
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引用次数: 0

摘要

在神经元中,大自噬/自噬是一个频繁而关键的过程。在轴突中,自噬开始于轴突末端,大多数新生自噬体在此形成。自噬体形成后,必须启动运输以离开轴突末端,并通过逆行运输向细胞体移动。在逆向运输过程中,这些自噬体通过重复的融合事件逐渐成熟。溶酶体货物的完全降解主要发生在细胞体内。刺激自噬体逆行运输的诱发事件一直存在争议,但其重要性是显而易见的:破坏神经元的自噬或自噬体运输会损害神经元的健康和功能。我们已经确定 HOPS 复合物对于早期自噬体成熟以及随后从轴突末端开始逆向运输至关重要。在酵母和哺乳动物细胞中,HOPS控制着自噬体和晚期内体与溶酶体之间的融合。我们利用HOPS复合体核心成分vps18和vps41功能缺失突变的斑马鱼品系,发现破坏HOPS会消除自噬体的成熟,并破坏自噬体从轴突末端开始的逆向运输。我们利用 Vps18 中 HOPS 结合结构域的内源性缺失,证实了这种表型是由于 HOPS 复合物形成的缺失造成的。最后,我们利用溶酶体蛋白酶的药理抑制,证明自噬体逆向运输的启动需要自噬体的成熟。我们的数据共同证明,HOPS 介导的融合事件是通过促进自噬体成熟启动自噬体逆向运输的关键。这揭示了 HOPS 复合物在神经元自噬中的关键作用,加深了我们对与 HOPS 复合物相关的神经退行性疾病的细胞病理学的理解:缩写:CORVET:缩写:CORVET:Class C core vacuole/endosome tethering;gRNA:引导 RNA;HOPS:同型融合和蛋白分选;pLL:后侧线;Vps18:CORVET 和 HOPS 复合物的 VPS18 核心亚基;Vps41:HOPS 复合物的 VPS41 亚基。
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An initial HOPS-mediated fusion event is critical for autophagosome transport initiation from the axon terminal.

In neurons, macroautophagy/autophagy is a frequent and critical process. In the axon, autophagy begins in the axon terminal, where most nascent autophagosomes form. After formation, autophagosomes must initiate transport to exit the axon terminal and move toward the cell body via retrograde transport. During retrograde transport these autophagosomes mature through repetitive fusion events. Complete lysosomal cargo degradation occurs largely in the cell body. The precipitating events to stimulate retrograde autophagosome transport have been debated but their importance is clear: disrupting neuronal autophagy or autophagosome transport is detrimental to neuronal health and function. We have identified the HOPS complex as essential for early autophagosome maturation and consequent initiation of retrograde transport from the axon terminal. In yeast and mammalian cells, HOPS controls fusion between autophagosomes and late endosomes with lysosomes. Using zebrafish strains with loss-of-function mutations in vps18 and vps41, core components of the HOPS complex, we found that disruption of HOPS eliminates autophagosome maturation and disrupts retrograde autophagosome transport initiation from the axon terminal. We confirmed this phenotype was due to loss of HOPS complex formation using an endogenous deletion of the HOPS binding domain in Vps18. Finally, using pharmacological inhibition of lysosomal proteases, we show that initiation of autophagosome retrograde transport requires autophagosome maturation. Together, our data demonstrate that HOPS-mediated fusion events are critical for retrograde autophagosome transport initiation through promoting autophagosome maturation. This reveals critical roles for the HOPS complex in neuronal autophagy which deepens our understanding of the cellular pathology of HOPS-complex linked neurodegenerative diseases.Abbreviations: CORVET: Class C core vacuole/endosome tethering; gRNA: guide RNA; HOPS: homotypic fusion and protein sorting; pLL: posterior lateral line; Vps18: VPS18 core subunit of CORVET and HOPS complexes; Vps41: VPS41 subunit of HOPS complex.

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