胞吐
细胞生物学
氧化应激
脂质过氧化
蛋白质聚集
程序性细胞死亡
化学
膜脂
生物
生物化学
细胞凋亡
分泌物
膜
作者
Isha Ralhan,Jinlan Chang,Matthew J. Moulton,Lindsey D. Goodman,Nathanael YJ Lee,Greg Plummer,H. Amalia Pasolli,Doreen Matthies,Hugo J. Bellen,Maria S. Ioannou
标识
DOI:10.1101/2022.11.24.517842
摘要
ABSTRACT During oxidative stress neurons release lipids that are internalized by glia. Defects in this coordinated process play an important role in several neurodegenerative diseases. Yet, the mechanisms of lipid release and its consequences on neuronal health are unclear. Here, we demonstrate that lipid-protein particle release by autolysosome exocytosis protects neurons from ferroptosis, a form of cell death driven by lipid peroxidation. We show that during oxidative stress, peroxidated lipids and iron are released from neurons by autolysosomal exocytosis which requires the exocytic machinery; VAMP7 and syntaxin 4. We observe membrane-bound lipid-protein particles by TEM and demonstrate that these particles are released from neurons using cryoEM. Failure to release these lipid-protein particles causes lipid hydroperoxide and iron accumulation and sensitizes neurons to ferroptosis. Our results reveal how neurons protect themselves from peroxidated lipids. Given the number of brain pathologies that involve ferroptosis, defects in this pathway likely play a key role in the pathophysiology of neurodegenerative disease. SUMMARY Release of lipid-protein particles by autolysosomal exocytosis protects neurons from ferroptosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI