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Abstract
The mitochondrial network continually undergoes events of fission and fusion. Under physiologic conditions, the network is in equilibrium and is characterized by the presence of both elongated and punctate mitochondria. However, this balanced, homeostatic mitochondrial profile can change morphologic distribution in response to various stressors. Therefore, it is imperative to develop a method that robustly measures mitochondrial morphology with high accuracy. Here, we developed a semi-automated image analysis pipeline for the quantitation of mitochondrial morphology for both in vitro and in vivo applications. The image analysis pipeline was generated and validated utilizing images of primary cortical neurons from transgenic mice, allowing genetic ablation of key components of mitochondrial dynamics. This analysis pipeline was further extended to evaluate mitochondrial morphology in vivo through immunolabeling of brain sections as well as serial block-face scanning electron microscopy. These data demonstrate a highly specific and sensitive method that accurately classifies distinct physiological and pathological mitochondrial morphologies. Furthermore, this workflow employs the use of readily available, free open-source software designed for high throughput image processing, segmentation, and analysis that is customizable to various biological models.
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Details
1 University of Michigan Medical School, Department of Emergency Medicine, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370); University of Michigan Medical School, Neuroscience Graduate Program, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370)
2 University of Michigan Medical School, Department of Emergency Medicine, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370); Wayne State University School of Medicine, Department of Physiology, Detroit, USA (GRID:grid.254444.7) (ISNI:0000 0001 1456 7807); University of Pittsburgh, Department of Human Genetics, Pittsburgh, USA (GRID:grid.21925.3d) (ISNI:0000 0004 1936 9000)
3 University of Michigan Medical School, Department of Emergency Medicine, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370)
4 University of Michigan Medical School, Department of Emergency Medicine, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370); University of Michigan Medical School, Frankel Cardiovascular Center, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370)
5 Wayne State University School of Medicine, Department of Physiology, Detroit, USA (GRID:grid.254444.7) (ISNI:0000 0001 1456 7807)
6 University of Michigan Medical School, Department of Emergency Medicine, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370); University of Michigan Medical School, Neuroscience Graduate Program, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370); University of Michigan Medical School, Frankel Cardiovascular Center, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370); University of Michigan Medical School, Department of Molecular and Integrative Physiology, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370)