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Loss of iron triggers PINK1/Parkin-independent mitophagy

In this study, we develop a simple assay to identify mitophagy inducers on the basis of the use of fluorescently tagged mitochondria that undergo a colour change on lysosomal delivery. Using this assay, we identify iron chelators as a family of compounds that generate a strong mitophagy response. Ir...

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Detalles Bibliográficos
Autores principales: Allen, George F G, Toth, Rachel, James, John, Ganley, Ian G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981094/
https://www.ncbi.nlm.nih.gov/pubmed/24176932
http://dx.doi.org/10.1038/embor.2013.168
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author Allen, George F G
Toth, Rachel
James, John
Ganley, Ian G
author_facet Allen, George F G
Toth, Rachel
James, John
Ganley, Ian G
author_sort Allen, George F G
collection PubMed
description In this study, we develop a simple assay to identify mitophagy inducers on the basis of the use of fluorescently tagged mitochondria that undergo a colour change on lysosomal delivery. Using this assay, we identify iron chelators as a family of compounds that generate a strong mitophagy response. Iron chelation-induced mitophagy requires that cells undergo glycolysis, but does not require PINK1 stabilization or Parkin activation, and occurs in primary human fibroblasts as well as those isolated from a Parkinson’s patient with Parkin mutations. Thus, we have identified and characterized a mitophagy pathway, the induction of which could prove beneficial as a potential therapy for several neurodegenerative diseases in which mitochondrial clearance is advantageous.
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spelling pubmed-39810942014-04-09 Loss of iron triggers PINK1/Parkin-independent mitophagy Allen, George F G Toth, Rachel James, John Ganley, Ian G EMBO Rep Scientific Reports In this study, we develop a simple assay to identify mitophagy inducers on the basis of the use of fluorescently tagged mitochondria that undergo a colour change on lysosomal delivery. Using this assay, we identify iron chelators as a family of compounds that generate a strong mitophagy response. Iron chelation-induced mitophagy requires that cells undergo glycolysis, but does not require PINK1 stabilization or Parkin activation, and occurs in primary human fibroblasts as well as those isolated from a Parkinson’s patient with Parkin mutations. Thus, we have identified and characterized a mitophagy pathway, the induction of which could prove beneficial as a potential therapy for several neurodegenerative diseases in which mitochondrial clearance is advantageous. European Molecular Biology Organization 2013-12 2013-11-01 /pmc/articles/PMC3981094/ /pubmed/24176932 http://dx.doi.org/10.1038/embor.2013.168 Text en Copyright © 2013, European Molecular Biology Organization https://creativecommons.org/licenses/by/3.0/This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. To view a copy of this licence visit http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Scientific Reports
Allen, George F G
Toth, Rachel
James, John
Ganley, Ian G
Loss of iron triggers PINK1/Parkin-independent mitophagy
title Loss of iron triggers PINK1/Parkin-independent mitophagy
title_full Loss of iron triggers PINK1/Parkin-independent mitophagy
title_fullStr Loss of iron triggers PINK1/Parkin-independent mitophagy
title_full_unstemmed Loss of iron triggers PINK1/Parkin-independent mitophagy
title_short Loss of iron triggers PINK1/Parkin-independent mitophagy
title_sort loss of iron triggers pink1/parkin-independent mitophagy
topic Scientific Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981094/
https://www.ncbi.nlm.nih.gov/pubmed/24176932
http://dx.doi.org/10.1038/embor.2013.168
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