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Autolysosomal exocytosis of lipids protect neurons from ferroptosis.
Ralhan, Isha; Chang, Jinlan; Moulton, Matthew J; Goodman, Lindsey D; Lee, Nathanael Y J; Plummer, Greg; Pasolli, H Amalia; Matthies, Doreen; Bellen, Hugo J; Ioannou, Maria S.
Afiliação
  • Ralhan I; Department of Physiology, University of Alberta, Edmonton, Canada.
  • Chang J; Group on Molecular and Cell Biology of Lipids, University of Alberta , Edmonton, Canada.
  • Moulton MJ; Department of Physiology, University of Alberta, Edmonton, Canada.
  • Goodman LD; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Lee NYJ; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital , Houston, TX, USA.
  • Plummer G; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Pasolli HA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital , Houston, TX, USA.
  • Matthies D; Department of Physiology, University of Alberta, Edmonton, Canada.
  • Bellen HJ; Group on Molecular and Cell Biology of Lipids, University of Alberta , Edmonton, Canada.
  • Ioannou MS; Faculty of Medicine & Dentistry Cell Imaging Core, University of Alberta , Edmonton, Canada.
J Cell Biol ; 222(6)2023 06 05.
Article em En | MEDLINE | ID: mdl-37036445
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Exocitose / Ferroptose / Lisossomos Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Exocitose / Ferroptose / Lisossomos Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article