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mito-QC illuminates mitophagy and mitochondrial architecture in vivo
Autophagic turnover of mitochondria, termed mitophagy, is proposed to be an essential quality-control (QC) mechanism of pathophysiological relevance in mammals. However, if and how mitophagy proceeds within specific cellular subtypes in vivo remains unclear, largely because of a lack of tractable to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4970326/ https://www.ncbi.nlm.nih.gov/pubmed/27458135 http://dx.doi.org/10.1083/jcb.201603039 |
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author | McWilliams, Thomas G. Prescott, Alan R. Allen, George F.G. Tamjar, Jevgenia Munson, Michael J. Thomson, Calum Muqit, Miratul M.K. Ganley, Ian G. |
author_facet | McWilliams, Thomas G. Prescott, Alan R. Allen, George F.G. Tamjar, Jevgenia Munson, Michael J. Thomson, Calum Muqit, Miratul M.K. Ganley, Ian G. |
author_sort | McWilliams, Thomas G. |
collection | PubMed |
description | Autophagic turnover of mitochondria, termed mitophagy, is proposed to be an essential quality-control (QC) mechanism of pathophysiological relevance in mammals. However, if and how mitophagy proceeds within specific cellular subtypes in vivo remains unclear, largely because of a lack of tractable tools and models. To address this, we have developed “mito-QC,” a transgenic mouse with a pH-sensitive fluorescent mitochondrial signal. This allows the assessment of mitophagy and mitochondrial architecture in vivo. Using confocal microscopy, we demonstrate that mito-QC is compatible with classical and contemporary techniques in histochemistry and allows unambiguous in vivo detection of mitophagy and mitochondrial morphology at single-cell resolution within multiple organ systems. Strikingly, our model uncovers highly enriched and differential zones of mitophagy in the developing heart and within specific cells of the adult kidney. mito-QC is an experimentally advantageous tool of broad relevance to cell biology researchers within both discovery-based and translational research communities. |
format | Online Article Text |
id | pubmed-4970326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49703262017-02-01 mito-QC illuminates mitophagy and mitochondrial architecture in vivo McWilliams, Thomas G. Prescott, Alan R. Allen, George F.G. Tamjar, Jevgenia Munson, Michael J. Thomson, Calum Muqit, Miratul M.K. Ganley, Ian G. J Cell Biol Research Articles Autophagic turnover of mitochondria, termed mitophagy, is proposed to be an essential quality-control (QC) mechanism of pathophysiological relevance in mammals. However, if and how mitophagy proceeds within specific cellular subtypes in vivo remains unclear, largely because of a lack of tractable tools and models. To address this, we have developed “mito-QC,” a transgenic mouse with a pH-sensitive fluorescent mitochondrial signal. This allows the assessment of mitophagy and mitochondrial architecture in vivo. Using confocal microscopy, we demonstrate that mito-QC is compatible with classical and contemporary techniques in histochemistry and allows unambiguous in vivo detection of mitophagy and mitochondrial morphology at single-cell resolution within multiple organ systems. Strikingly, our model uncovers highly enriched and differential zones of mitophagy in the developing heart and within specific cells of the adult kidney. mito-QC is an experimentally advantageous tool of broad relevance to cell biology researchers within both discovery-based and translational research communities. The Rockefeller University Press 2016-08-01 /pmc/articles/PMC4970326/ /pubmed/27458135 http://dx.doi.org/10.1083/jcb.201603039 Text en © 2016 McWilliams et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles McWilliams, Thomas G. Prescott, Alan R. Allen, George F.G. Tamjar, Jevgenia Munson, Michael J. Thomson, Calum Muqit, Miratul M.K. Ganley, Ian G. mito-QC illuminates mitophagy and mitochondrial architecture in vivo |
title | mito-QC illuminates mitophagy and mitochondrial architecture in vivo |
title_full | mito-QC illuminates mitophagy and mitochondrial architecture in vivo |
title_fullStr | mito-QC illuminates mitophagy and mitochondrial architecture in vivo |
title_full_unstemmed | mito-QC illuminates mitophagy and mitochondrial architecture in vivo |
title_short | mito-QC illuminates mitophagy and mitochondrial architecture in vivo |
title_sort | mito-qc illuminates mitophagy and mitochondrial architecture in vivo |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4970326/ https://www.ncbi.nlm.nih.gov/pubmed/27458135 http://dx.doi.org/10.1083/jcb.201603039 |
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