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Updated: Jul 2, 2026

Assessment of Mitochondrial Fission/Fusion Dynamics in Kidney Proximal Tubular Cells
Published on: November 14, 2025
Novel mitochondrial extensions provide evidence for a link between microtubule-directed movement and mitochondrial
Timothy Bowes1, Radhey S Gupta
1Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada L8N3Z5.
Abstract:
Mitochondrial dynamics play an important role in a large number of cellular processes. Previously, we reported that treatment of mammalian cells with the cysteine-alkylators, N-ethylmaleimide and ethacrynic acid, induced rapid mitochondrial fusion forming a large reticulum approximately 30 min after treatment. Here, we further investigated this phenomenon using a number of techniques including live-cell confocal microscopy. In live cells, drug-induced fusion coincided with a cessation of fast mitochondrial movement which was dependent on microtubules. During this loss of movement, thin mitochondrial tubules extending from mitochondria were also observed, which we refer to as 'mitochondrial extensions'. The formation of these mitochondrial extensions, which were not observed in untreated cells, depended on microtubules and was abolished by pretreatment with nocodazole. In this study, we provide evidence that these extensions result from of a block in mitochondrial fission combined with continued application of motile force by microtubule-dependent motor complexes. Our observations strongly suggest the existence of a link between microtubule-based mitochondrial trafficking and mitochondrial fission.
Insights
Chemicals that alter mitochondrial dynamics trigger rapid mitochondrial fusion and unique extensions. This study reveals a link between microtubule-based movement and mitochondrial fission.
Area of Science:
- Cell Biology
- Mitochondrial Biology
- Cytoskeletal Dynamics
Background:
- Mitochondrial dynamics are crucial for cellular functions.
- Previous work showed cysteine-alkylators induce mitochondrial fusion in mammalian cells.
Purpose of the Study:
- Investigate the mechanisms behind drug-induced mitochondrial fusion.
- Explore the role of microtubules in mitochondrial dynamics and morphology.
Main Methods:
- Live-cell confocal microscopy
- Treatment with cysteine-alkylators (N-ethylmaleimide, ethacrynic acid)
- Microtubule disruption using nocodazole
Main Results:
- Drug treatment caused rapid mitochondrial fusion and cessation of movement.
- Observed novel 'mitochondrial extensions' dependent on microtubules.
- Extensions formation linked to blocked fission and microtubule-motor activity.
Conclusions:
- Microtubule-based mitochondrial trafficking is linked to mitochondrial fission.
- Cessation of movement and extension formation result from impaired fission.
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