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Repetitive transient depolarizations of the inner mitochondrial membrane induced by proton pumping
Authors:Hattori Tomohiro  Watanabe Koichi  Uechi Yukiko  Yoshioka Hisashi  Ohta Yoshihiro
Affiliation:Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, Nakacho, Koganei, Tokyo 184-8588, Japan.
Abstract:Single mitochondria show the spontaneous fluctuations of DeltaPsim. In this study, to examine the mechanism of the fluctuations, we observed DeltaPsim in single isolated heart mitochondria using time-resolved fluorescence microscopy. Addition of malate, succinate, or ascorbate plus TMPD to mitochondria induced polarization of the inner membrane followed by repeated cycles of rapid depolarizations and immediate repolarizations. ADP significantly decreased the frequency of the rapid depolarizations, but the ADP effect was counteracted by oligomycin. On the other hand, the rapid depolarizations did not occur when mitochondria were polarized by the efflux of K(+) from the matrix. The rapid depolarizations became frequent with the increase in the substrate concentration or pH of the buffer. These results suggest that the rapid depolarizations depend on the net translocation of protons from the matrix. The frequency of the rapid depolarizations was not affected by ROS scavengers, Ca(2+), CsA, or BA. In addition, the obvious increase in the permeability of the inner membrane to calcein (MW 623) that was entrapped in the matrix was not observed upon the transient depolarization. The mechanisms of the spontaneous oscillations of DeltaPsim are discussed in relation to the matrix pH and the permeability transitions.
Keywords:ΔΨm, mitochondrial membrane potential   ANT, adenine nucleotide translocator   BA, bongkrekic acid   BCA, bicinchoninic acid   BSA, bovine serum albumin   calcein-AM, calcein acetoxymethyl ester   CsA, cyclosporin A   DTT, dithiothreitol   GSH, reduced glutathione   IMAC, mitochondrial inner membrane anion channel   MPT, mitochondrial permeability transition   ROS, reactive oxygen species   TMPD, tetramethyl-p-phenylenediamine   TMPyP, Mn(III)tetrakis(1-methyl-4-pyridil)porphyrin pentachloride
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