Imaging the Permeability Pore Transition in Single Mitochondria

• Published in: Biophysical journal 1998-04, Vol.74 (4), p.2129-2137
• Main Authors: Hüser, Jörg, Rechenmacher, Christine E., Blatter, Lothar A.
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - metabolism; Animals; Biophysical Phenomena; Biophysics; Calcium - metabolism; Cyclosporine - pharmacology; Glutathione - pharmacology; In Vitro Techniques; Intracellular Membranes - drug effects; Intracellular Membranes - metabolism; Intracellular Membranes - radiation effects; Ion Channel Gating; Light; Membrane Potentials; Mitochondria, Heart - drug effects; Mitochondria, Heart - metabolism; Mitochondria, Heart - radiation effects; Permeability; Rats; Reactive Oxygen Species - metabolism
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/S0006-3495(98)77920-2

In mitochondria the opening of a large proteinaceous pore, the “mitochondrial permeability transition pore” (MTP), is known to occur under conditions of oxidative stress and matrix calcium overload. MTP opening and the resulting cellular energy deprivation have been implicated in processes such as hypoxic cell damage, apoptosis, and neuronal excitotoxicity. Membrane potential (ΔΨ m) in single isolated heart mitochondria was measured by confocal microscopy with a voltage-sensitive fluorescent dye. Measurements in mitochondrial populations revealed a gradual loss of ΔΨ m due to the light-induced generation of free radicals. In contrast, the depolarization in individual mitochondria was fast, sometimes causing marked oscillations of ΔΨ m. Rapid depolarizations were accompanied by an increased permeability of the inner mitochondrial membrane to matrix-entrapped calcein (≈620 Da), indicating the opening of a large membrane pore. The MTP inhibitor cyclosporin A significantly stabilized ΔΨ m in single mitochondria, thereby slowing the voltage decay in averaged recordings. We conclude that the spontaneous depolarizations were caused by repeated stochastic openings and closings of the transition pore. The data demonstrate a much more dynamic regulation of membrane permeability at the level of a single organelle than predicted from ensemble behavior of mitochondrial populations.