The autophagy protein ATG-9 regulates lysosome function and integrity.

IF 7.4 1区 生物学 Q1 CELL BIOLOGY
Journal of Cell Biology Pub Date : 2025-06-02 Epub Date: 2025-04-09 DOI:10.1083/jcb.202411092
Kangfu Peng, Guoxiu Zhao, Hongyu Zhao, Nobuo N Noda, Hong Zhang
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引用次数: 0

Abstract

The transmembrane autophagy protein ATG9 has multiple functions essential for autophagosome formation. Here, we uncovered a novel function of ATG-9 in regulating lysosome biogenesis and integrity in Caenorhabditis elegans. Through a genetic screen, we identified that mutations attenuating the lipid scrambling activity of ATG-9 suppress the autophagy defect in epg-5 mutants, in which non-degradative autolysosomes accumulate. The scramblase-attenuated ATG-9 mutants promote lysosome biogenesis and delivery of lysosome-localized hydrolases and also facilitate the maintenance of lysosome integrity. Through manipulation of phospholipid levels, we found that a reduction in phosphatidylethanolamine (PE) also suppresses the autophagy defects and lysosome damage associated with impaired lysosomal degradation. Our results reveal that modulation of phospholipid composition and distribution, e.g., by attenuating the scramblase activity of ATG-9 or reducing the PE level, regulates lysosome function and integrity.

自噬蛋白ATG-9调节溶酶体的功能和完整性。
跨膜自噬蛋白ATG9在自噬体形成中具有多种功能。在这里,我们发现了ATG-9在调节秀丽隐杆线虫溶酶体生物发生和完整性方面的新功能。通过基因筛选,我们发现,降低ATG-9脂质混乱活性的突变抑制了epg-5突变体的自噬缺陷,其中不可降解的自噬酶体积累。减弱的ATG-9突变体促进了溶酶体的生物发生和溶酶体定位水解酶的传递,也促进了溶酶体完整性的维持。通过操纵磷脂水平,我们发现磷脂酰乙醇胺(PE)的减少也抑制自噬缺陷和溶酶体降解受损相关的溶酶体损伤。我们的研究结果表明,磷脂组成和分布的调节,例如,通过减弱ATG-9的超燃酶活性或降低PE水平,调节溶酶体的功能和完整性。
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来源期刊
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
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