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1000 Titel
  • Ferroptosis inhibitor improves outcome after early and delayed treatment in mild spinal cord injury
1000 Autor/in
  1. Ryan, Fari |
  2. Blex, Christian |
  3. Ngo, The Dung |
  4. Kopp, Marcel A. |
  5. Michalke, Bernhard |
  6. Venkataramani, Vivek |
  7. Curran, Laura |
  8. Schwab, Jan M. |
  9. Ruprecht, Klemens |
  10. Otto, Carolin |
  11. Jhelum, Priya |
  12. Kroner, Antje |
  13. JHELUM, PRIYA |
1000 Verlag Springer Berlin Heidelberg
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-06-22
1000 Erschienen in
1000 Quellenangabe
  • 147(1):106
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-024-02758-2 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11193702/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>We show that redox active iron can induce a regulated form of non-apoptotic cell death and tissue damage called ferroptosis that can contribute to secondary damage and functional loss in the acute and chronic periods after spinal cord injury (SCI) in young, adult, female mice. Phagocytosis of red blood cells at sites of hemorrhage is the main source of iron derived from hemoglobin after SCI. Expression of hemeoxygenase-1 that induces release of iron from heme, is increased in spinal cord macrophages 7 days after injury. While iron is stored safely in ferritin in the injured spinal cord, it can, however, be released by NCOA4-mediated shuttling of ferritin to autophagosomes for degradation (ferritinophagy). This leads to the release of redox active iron that can cause free radical damage. Expression of NCOA4 is increased after SCI, mainly in macrophages. Increase in the ratio of redox active ferrous (Fe<jats:sup>2+</jats:sup>) to ferric iron (Fe<jats:sup>3+</jats:sup>) is also detected after SCI by capillary electrophoresis inductively coupled mass spectrometry. These changes are accompanied by other hallmarks of ferroptosis, i.e., deficiency in various elements of the antioxidant glutathione (GSH) pathway. We also detect increases in enzymes that repair membrane lipids (ACSL4 and LPCAT3) and thus promote on-going ferroptosis. These changes are associated with increased levels of 4-hydroxynonenal (4-HNE), a toxic lipid peroxidation product. Mice with mild SCI (30 kdyne force) treated with the ferroptosis inhibitor (UAMC-3203-HCL) either early or delayed times after injury showed improvement in locomotor recovery and secondary damage. Cerebrospinal fluid and serum samples from human SCI cases show evidence of increased iron storage (ferritin), and other iron related molecules, and reduction in GSH. Collectively, these data suggest that ferroptosis contributes to secondary damage after SCI and highlights the possible use of ferroptosis inhibitors to treat SCI.</jats:p>
1000 Sacherschließung
lokal Iron/metabolism [MeSH]
lokal Female [MeSH]
lokal Spinal Cord Injuries/drug therapy [MeSH]
lokal Mice, Inbred C57BL [MeSH]
lokal Spinal cord injury
lokal NCOA4
lokal Antioxidants
lokal Ferroptosis/physiology [MeSH]
lokal Animals [MeSH]
lokal Ferroptosis/drug effects [MeSH]
lokal Iron toxicity
lokal Ferritin
lokal Mice [MeSH]
lokal Original Paper
lokal Spinal Cord Injuries/metabolism [MeSH]
lokal Spinal Cord Injuries/pathology [MeSH]
lokal Treatment Delay [MeSH]
lokal Lipid peroxidation
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/UnlhbiwgRmFyaQ==|https://frl.publisso.de/adhoc/uri/QmxleCwgQ2hyaXN0aWFu|https://frl.publisso.de/adhoc/uri/TmdvLCBUaGUgRHVuZw==|https://frl.publisso.de/adhoc/uri/S29wcCwgTWFyY2VsIEEu|https://frl.publisso.de/adhoc/uri/TWljaGFsa2UsIEJlcm5oYXJk|https://frl.publisso.de/adhoc/uri/VmVua2F0YXJhbWFuaSwgVml2ZWs=|https://frl.publisso.de/adhoc/uri/Q3VycmFuLCBMYXVyYQ==|https://frl.publisso.de/adhoc/uri/U2Nod2FiLCBKYW4gTS4=|https://frl.publisso.de/adhoc/uri/UnVwcmVjaHQsIEtsZW1lbnM=|https://frl.publisso.de/adhoc/uri/T3R0bywgQ2Fyb2xpbg==|https://frl.publisso.de/adhoc/uri/SmhlbHVtLCBQcml5YQ==|https://frl.publisso.de/adhoc/uri/S3JvbmVyLCBBbnRqZQ==|https://orcid.org/0000-0003-0779-2816
1000 Hinweis
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1000 Förderer
  1. Wings for Life |
  2. Canadian Institutes of Health Research |
  3. Else Kröner-Fresenius-Stiftung |
  4. Deutsche Forschungsgemeinschaft |
  5. National Institute of Neurological Disorders and Stroke |
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    1000 Förderer Canadian Institutes of Health Research |
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    1000 Förderer Else Kröner-Fresenius-Stiftung |
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    1000 Förderer Deutsche Forschungsgemeinschaft |
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    1000 Förderer National Institute of Neurological Disorders and Stroke |
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1000 Erstellt am 2025-02-03T17:37:57.791+0100
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