2025/01/09 by Julie Faitg, Tracey Davey, Ross Laws +5 · 1 voice · 1 citation
Biochemistry, Genetics and Molecular Biology · #ATP Synthase and ATPases Research #Metabolism and Genetic Disorders #Mitochondrial Function and Pathology
paper · pdf · doi:10.1038/s42003-024-07389-7
openalex publication_date 2025/01/09 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/23
Mitochondria play a crucial role in maintaining cellular health. It is interesting that the shape of mitochondria can vary depending on the type of cell, mitochondrial function, and other cellular conditions. However, there are limited studies that link functional assessment with mitochondrial morphology evaluation at high magnification, even fewer that do so in situ and none in human muscle biopsies. Therefore, we have developed a method which combines functional assessment of mitochondria through Cytochrome c Oxidase (COX) histochemistry, with a 3D electron microscopy (EM) technique, serial block-face scanning electron microscopy (SBFSEM). Here we apply COX-SBFSEM to muscle samples from patients with single, large-scale mtDNA deletions, a cause of mitochondrial disease. These deletions cause oxidative phosphorylation deficiency, which can be observed through changes in COX activity. One of the main advantages of combining 3D-EM with the COX reaction is the ability to look at how per-mitochondrion oxidative phosphorylation status is spatially distributed within muscle fibres. Here we show a robust spatial pattern in COX-positive and intermediate-fibres and that the spatial pattern is less clear in COX-deficient fibres.