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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2013
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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. |
format | Online Article Text |
id | pubmed-3981094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
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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