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Updated: Jun 23, 2026

Isolation and Functional Analysis of Mitochondria from Cultured Cells and Mouse Tissue
Published on: March 23, 2015
Mitochondrial outer-membrane permeabilization and remodelling in apoptosis
Alexis Jourdain1, Jean-Claude Martinou
1Department of Cell Biology, University of Geneva, Quai Ernest-Ansermet 30, 1211 Geneva 4, Switzerland.
Abstract:
Many human pathologies are associated with defects in mitochondria such as diabetes, neurodegenerative diseases or cancer. This tiny organelle is involved in a plethora of processes in mammalian cells, including energy production, lipid metabolism and cell death. In the so-called intrinsic apoptotic pathway, the outer mitochondrial membrane (MOM) is premeabilized by the pro-apoptotic Bcl-2 members Bax and Bak, allowing the release of apoptogenic factors such as cytochrome c from the inter-membrane space into the cytosol. At the same time, mitochondria fragment in response to Drp-1 activation suggesting that mitochondrial fission could play a role in mitochondrial outer-membrane permeabilization (MOMP). In this review, we will discuss the link that could exist between mitochondrial fission and fusion machinery, Bcl-2 family members and MOMP.
Insights
Mitochondrial fission, regulated by Bcl-2 family proteins, may trigger outer mitochondrial membrane permeabilization (MOMP). This process is crucial for programmed cell death and implicated in various human diseases.
Area of Science:
- Cell Biology
- Molecular Biology
- Pathology
Background:
- Mitochondria are vital organelles involved in energy production, metabolism, and cell death.
- Defects in mitochondria are linked to diseases like diabetes, neurodegeneration, and cancer.
- The intrinsic apoptotic pathway involves outer mitochondrial membrane permeabilization (MOMP) mediated by Bax and Bak, releasing cytochrome c.
Purpose of the Study:
- To explore the potential link between mitochondrial fission and outer mitochondrial membrane permeabilization (MOMP).
- To review the roles of mitochondrial fission/fusion machinery and Bcl-2 family members in MOMP.
Main Methods:
- This is a review article, synthesizing existing research.
- Discussion focuses on the interplay between mitochondrial dynamics and apoptosis.
Main Results:
- Mitochondrial fragmentation, driven by Drp-1 activation, is observed during MOMP.
- This suggests a functional connection between mitochondrial fission and the initiation of apoptosis.
Conclusions:
- Mitochondrial fission machinery and Bcl-2 family proteins are key players in MOMP.
- Understanding this link is critical for deciphering mitochondrial roles in human pathologies.
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