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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...

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Autores principales: McWilliams, Thomas G., Prescott, Alan R., Allen, George F.G., Tamjar, Jevgenia, Munson, Michael J., Thomson, Calum, Muqit, Miratul M.K., Ganley, Ian G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
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.
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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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