Autolysosomal exocytosis of lipids protect neurons from ferroptosis

Author:

Ralhan Isha12ORCID,Chang Jinlan1ORCID,Moulton Matthew J.34ORCID,Goodman Lindsey D.34ORCID,Lee Nathanael Y.J.12ORCID,Plummer Greg5ORCID,Pasolli H. Amalia67ORCID,Matthies Doreen8ORCID,Bellen Hugo J.349ORCID,Ioannou Maria S.121011ORCID

Affiliation:

1. University of Alberta 1 Department of Physiology, , Edmonton, Canada

2. Group on Molecular and Cell Biology of Lipids, University of Alberta 2 , Edmonton, Canada

3. Baylor College of Medicine 3 Department of Molecular and Human Genetics, , Houston, TX, USA

4. Jan and Dan Duncan Neurological Research Institute, Texas Children’s Hospital 4 , Houston, TX, USA

5. Faculty of Medicine & Dentistry Cell Imaging Core, University of Alberta 5 , Edmonton, Canada

6. Electron Microscopy Resource Center, The Rockefeller University 6 , New York, NY, USA

7. Janelia Research Campus, Howard Hughes Medical Institute 7 , Ashburn, VA, USA

8. Unit on Structural Biology, Division of Basic and Translational Biophysics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health 8 , Bethesda, MD, USA

9. Department of Neuroscience, Baylor College of Medicine 9 , Houston, TX, USA

10. Department of Cell Biology, University of Alberta 10 , Edmonton, Canada

11. Neuroscience and Mental Health Institute, University of Alberta 11 , Edmonton, Canada

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.

Funder

Canadian Institutes of Health Research

Alzheimer Society

University Hospital Foundation

Neuroscience and Mental Health Institute

Faculty of Medicine and Dentistry, University of Alberta

National Institutes of Health

BrightFocus Foundation

Howard Hughes Medical Institute

National Institute on Aging

NIH Office of the Director

NHLBI Division of Intramural Research

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Heart and Stroke Foundation of Canada

Canadian Foundation for Innovation

Publisher

Rockefeller University Press

Subject

Cell Biology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The mechanism of ferroptosis and its related diseases;Molecular Biomedicine;2023-10-16

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3