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Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration

Even after decades of research, the mechanism of neurodegeneration remains understudied, hindering the discovery of effective treatments for neurodegenerative diseases. Recent reports suggest that ferroptosis could be a novel therapeutic target for neurodegenerative diseases. While polyunsaturated f...

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Autores principales: Sarparast, Morteza, Pourmand, Elham, Hinman, Jennifer, Vonarx, Derek, Reason, Tommy, Zhang, Fan, Paithankar, Shreya, Chen, Bin, Borhan, Babak, Watts, Jennifer L., Alan, Jamie, Lee, Kin Sing Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881903/
https://www.ncbi.nlm.nih.gov/pubmed/36711920
http://dx.doi.org/10.1101/2023.01.05.522933
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author Sarparast, Morteza
Pourmand, Elham
Hinman, Jennifer
Vonarx, Derek
Reason, Tommy
Zhang, Fan
Paithankar, Shreya
Chen, Bin
Borhan, Babak
Watts, Jennifer L.
Alan, Jamie
Lee, Kin Sing Stephen
author_facet Sarparast, Morteza
Pourmand, Elham
Hinman, Jennifer
Vonarx, Derek
Reason, Tommy
Zhang, Fan
Paithankar, Shreya
Chen, Bin
Borhan, Babak
Watts, Jennifer L.
Alan, Jamie
Lee, Kin Sing Stephen
author_sort Sarparast, Morteza
collection PubMed
description Even after decades of research, the mechanism of neurodegeneration remains understudied, hindering the discovery of effective treatments for neurodegenerative diseases. Recent reports suggest that ferroptosis could be a novel therapeutic target for neurodegenerative diseases. While polyunsaturated fatty acid (PUFA) plays an important role in neurodegeneration and ferroptosis, how PUFAs may trigger these processes remains largely unknown. PUFA metabolites from cytochrome P450 and epoxide hydrolase metabolic pathways may modulate neurodegeneration. Here, we test the hypothesis that specific PUFAs regulate neurodegeneration through the action of their downstream metabolites by affecting ferroptosis. We find that the PUFA, dihomo gamma linolenic acid (DGLA), specifically induces ferroptosis-mediated neurodegeneration in dopaminergic neurons. Using synthetic chemical probes, targeted metabolomics, and genetic mutants, we show that DGLA triggers neurodegeneration upon conversion to dihydroxyeicosadienoic acid through the action of CYP-EH, representing a new class of lipid metabolite that induces neurodegeneration via ferroptosis.
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spelling pubmed-98819032023-01-28 Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration Sarparast, Morteza Pourmand, Elham Hinman, Jennifer Vonarx, Derek Reason, Tommy Zhang, Fan Paithankar, Shreya Chen, Bin Borhan, Babak Watts, Jennifer L. Alan, Jamie Lee, Kin Sing Stephen bioRxiv Article Even after decades of research, the mechanism of neurodegeneration remains understudied, hindering the discovery of effective treatments for neurodegenerative diseases. Recent reports suggest that ferroptosis could be a novel therapeutic target for neurodegenerative diseases. While polyunsaturated fatty acid (PUFA) plays an important role in neurodegeneration and ferroptosis, how PUFAs may trigger these processes remains largely unknown. PUFA metabolites from cytochrome P450 and epoxide hydrolase metabolic pathways may modulate neurodegeneration. Here, we test the hypothesis that specific PUFAs regulate neurodegeneration through the action of their downstream metabolites by affecting ferroptosis. We find that the PUFA, dihomo gamma linolenic acid (DGLA), specifically induces ferroptosis-mediated neurodegeneration in dopaminergic neurons. Using synthetic chemical probes, targeted metabolomics, and genetic mutants, we show that DGLA triggers neurodegeneration upon conversion to dihydroxyeicosadienoic acid through the action of CYP-EH, representing a new class of lipid metabolite that induces neurodegeneration via ferroptosis. Cold Spring Harbor Laboratory 2023-01-10 /pmc/articles/PMC9881903/ /pubmed/36711920 http://dx.doi.org/10.1101/2023.01.05.522933 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Sarparast, Morteza
Pourmand, Elham
Hinman, Jennifer
Vonarx, Derek
Reason, Tommy
Zhang, Fan
Paithankar, Shreya
Chen, Bin
Borhan, Babak
Watts, Jennifer L.
Alan, Jamie
Lee, Kin Sing Stephen
Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration
title Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration
title_full Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration
title_fullStr Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration
title_full_unstemmed Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration
title_short Dihydroxy-Metabolites of Dihomo-gamma-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration
title_sort dihydroxy-metabolites of dihomo-gamma-linolenic acid drive ferroptosis-mediated neurodegeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881903/
https://www.ncbi.nlm.nih.gov/pubmed/36711920
http://dx.doi.org/10.1101/2023.01.05.522933
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