从宝藏中分类垃圾:轴突中自噬和内吞运输的不同途径

Autophagy reports Pub Date : 2023-01-19 eCollection Date: 2023-01-01 DOI:10.1080/27694127.2023.2166322
Vineet Vinay Kulkarni, Sandra Maday
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摘要

巨噬(以下简称自噬)和内吞运输是神经元轴突调节轴突蛋白质组组成和完整性的关键途径。这些途径有类似的贩运路线;然而,他们的相声程度仍不完全清楚。我们最近的工作表明,在生理条件下,轴突自噬和内吞途径是分开的,并表现出不同的细胞器成熟速度。引人注目的是,致病性α-突触核蛋白的过度表达通过合并远端轴突产生的自噬体和核内体,破坏了这些途径之间的分离。这些结果提出了一种可能性,即内吞货物通过错误路径进入溶酶体归宿的自噬体而过早降解可能导致帕金森病和相关α-突触核蛋白病的神经元功能障碍。
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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Sorting trash from treasure: Separate pathways for autophagy and endocytic trafficking in axons.

Macroautophagy (hereafter autophagy) and endocytic trafficking are key pathways in neuronal axons that regulate the composition and integrity of the axonal proteome. These pathways have similar trafficking itineraries; however, the extent of their cross-talk remains incompletely understood. Our recent work demonstrates that under physiological conditions, axonal autophagy and endocytic pathways are separate and exhibit distinct rates of organelle maturation. Strikingly, overexpression of pathogenic α-synuclein disrupts the segregation between these pathways by merging autophagosomes and endosomes generated in the distal axon. These results raise the possibility that precocious degradation of endocytosed cargo via misrouting into lysosome-destined autophagosomes may contribute to neuronal dysfunction in Parkinson disease and related α-synucleinopathies.

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