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Updated: Aug 16, 2026

Understanding the Changes in Mitochondrial Morphology through Dynamic and Three-dimensional Fluorescence Micrographs
Published on: August 15, 2025
Molecular basis of morphological changes in mitochondrial membrane accompanying induction of permeability transition,
Satsuki Terauchi1, Takenori Yamamoto, Kikuji Yamashita
1Institute for Genome Research, University of Tokushima, Kuramotocho-3, Tokushima 770-8503, Japan.
Abstract:
The mitochondrial inner membrane typically shows a condensed structure when examined by electron microscopy. However, this typical structure is known to disappear upon induction of the mitochondrial permeability transition (PT). This change in the appearance of the mitochondrial membrane structure that accompanies the induction of PT is thought to reflect changes in the permeability of inner mitochondrial membrane; however, its molecular basis has remained uncertain. In the present study, changes in membrane status were examined by immuno-electron microscopy using antibodies against the voltage-dependent anion channel (VDAC), beta-subunit of F1-ATPase (F1beta), and cytochrome c (cyt. c). In control mitochondria, antibody against VDAC was observed at the rim of the mitochondria, whereas antibodies against F1beta and cytochrome c bound these molecules inside of the mitochondria. However, in PT-induced mitochondria, all three antibodies were observed at the mitochondrial rim. These results strongly suggest that the inner mitochondrial membrane is shoved to the rim region of mitochondria upon induction of mitochondrial PT.
Insights
The mitochondrial inner membrane structure changes during permeability transition (PT). Researchers used immuno-electron microscopy to show the inner membrane shifts to the mitochondrial rim during PT.
Area of Science:
- Mitochondrial biology
- Cellular biophysics
Background:
- The mitochondrial inner membrane's condensed structure changes during permeability transition (PT).
- The molecular basis for this structural change and its relation to inner mitochondrial membrane permeability remains unclear.
Purpose of the Study:
- To investigate the molecular basis of structural changes in the mitochondrial inner membrane during PT.
- To determine the localization of key mitochondrial proteins during PT induction.
Main Methods:
- Immuno-electron microscopy was employed to visualize protein localization.
- Antibodies against voltage-dependent anion channel (VDAC), F1-ATPase beta-subunit (F1beta), and cytochrome c (cyt. c) were used.
Main Results:
- In control mitochondria, VDAC was at the rim, while F1beta and cyt. c were inside.
- Upon PT induction, VDAC, F1beta, and cyt. c were all observed at the mitochondrial rim.
- This indicates a significant structural rearrangement of the inner mitochondrial membrane.
Conclusions:
- The study provides strong evidence that the inner mitochondrial membrane is displaced to the rim region during PT.
- This finding offers insights into the structural dynamics of mitochondria during permeability transition events.
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