Peng Kangfu, Zhao Guoxiu, Zhao Hongyu, Noda Nobuo N, Zhang Hong
National Laboratory of Biomacromolecules, New Cornerstone Science Laboratory, Institute of Biophysics, Chinese Academy of Sciences, Beijing, P.R. China.
College of Life Sciences, University of Chinese Academy of Sciences , Beijing, P.R. China.
J Cell Biol. 2025 Jun 2;224(6). doi: 10.1083/jcb.202411092. Epub 2025 Apr 9.
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.
跨膜自噬蛋白ATG9具有自噬体形成所必需的多种功能。在此,我们揭示了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,我们发现减弱ATG-9脂质翻转活性的突变可抑制epg-5突变体中的自噬缺陷,在该突变体中会积累非降解性自噬溶酶体。脂质翻转酶减弱的ATG-9突变体促进溶酶体生物发生以及溶酶体定位水解酶的递送,并且还有助于维持溶酶体完整性。通过操纵磷脂水平,我们发现磷脂酰乙醇胺(PE)的减少也可抑制与溶酶体降解受损相关的自噬缺陷和溶酶体损伤。我们的结果表明,例如通过减弱ATG-9的脂质翻转酶活性或降低PE水平来调节磷脂组成和分布,可调控溶酶体功能和完整性。