Autolysosomal exocytosis of lipids protect neurons from ferroptosis

Isha Ralhan, Jinlan Chang, M. Moulton, Lindsey D. Goodman, Nathanael Lee, Gregory Plummer, H. Pasolli, D. Matthies, H. Bellen, Maria S. Ioannou
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引用次数: 1

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.
脂质自溶酶体胞吐保护神经元免于铁下垂
在氧化应激过程中,神经元释放脂质,脂质被神经胶质内化。这种协调过程中的缺陷在几种神经退行性疾病中起重要作用。然而,脂质释放的机制及其对神经元健康的影响尚不清楚。在这里,我们证明了自溶酶体胞吐释放的脂质蛋白颗粒可以保护神经元免受铁死亡,铁死亡是一种由脂质过氧化驱动的细胞死亡形式。我们发现,在氧化应激过程中,过氧化脂质和铁通过自溶酶体胞吐作用从神经元中释放出来,这需要胞吐机制;VAMP7和syntaxin 4。我们通过透射电镜观察到膜结合的脂质蛋白颗粒,并通过低温电镜证明这些颗粒从神经元中释放出来。不能释放这些脂质蛋白颗粒会导致脂质过氧化氢和铁积累,并使神经元对铁下垂敏感。我们的研究结果揭示了神经元如何保护自己免受过氧化脂质的侵害。考虑到涉及铁下垂的脑病理的数量,该通路的缺陷可能在神经退行性疾病的病理生理中起关键作用。自溶酶体胞吐释放脂质蛋白颗粒保护神经元免于铁下垂。
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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