mito-QC illuminates mitophagy and mitochondrial architecture in vivo

Author:

McWilliams Thomas G.1,Prescott Alan R.23ORCID,Allen George F.G.1,Tamjar Jevgenia1,Munson Michael J.1ORCID,Thomson Calum3,Muqit Miratul M.K.14,Ganley Ian G.1ORCID

Affiliation:

1. Medical Research Council Protein Phosphorylation and Ubiquitylation Unit, University of Dundee, Dundee DD1 9SY, Scotland, UK

2. Division of Cell Signalling and Immunology, University of Dundee, Dundee DD1 9SY, Scotland, UK

3. Dundee Imaging Facility, School of Life Sciences, University of Dundee, Dundee DD1 9SY, Scotland, UK

4. School of Medicine, University of Dundee, Dundee DD1 9SY, Scotland, UK

Abstract

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.

Funder

Medical Research Council

Wellcome Trust

Publisher

Rockefeller University Press

Subject

Cell Biology

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