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A mitochondrial self-preservation mechanism

When the balance of proton influx and efflux is lost and theproton inside the mitochondria is insufficient, the amount of ROS generated increases. Proton deficiency inside the mitochondria induces proton influx from the emergency route. Once the proton shortage inside the mitochondria is resolved, the emergency route is closed. Credit: Yoshihiro Ohta/ TUAT

Mitochondria, the powerhouse of the cell, convert sustenance into energy, fueling the cell’s activities. In addition to power, mitochondria also produce reactive oxygen species, byproduct molecules primed to help facilitate communication among the other units in the cells. But when produced too abundantly, they damage DNA and render some cellular components dysfunctional. Now, an international research team has revealed how mitochondria keep their reactive oxygen species production in check.


They published their results on June 30 in Frontiers in Cell and Developmental Biology.

“Excessive generation of reactive oxygen species in mitochondria damages mitochondria and reduces cell function, so the mechanism by which mitochondria maintain production of reactive oxygen species is crucial for cells,” said lead paper author Yoshihiro Ohta, associate professor in the Department of Biotechnology and Life Science at Tokyo University of Agriculture and Technology in Japan. “In this study, we found that mitochondria have a mechanism to spontaneously avoid the production of excess reactive oxygen species.”

Mitochondria are double membraned, with genetic information and functional units contained within its internal matrix. Mitochondria convert chemical energy into power for the cell by moving protons from outside to inside the matrix with the help of an enzyme responsible for energy conversion. But mitochondria also appear to impulsively and temporarily take up protons through another protein through a process called spontaneous transient depolarization.

In a video, mitochondria in rat cardiomyocytes (H9c2) are shown.Mitochondria (white strings) pump out protons and have an internal negative membrane potential. In the yellow ring, the membrane potential of the mitochondria is rapidly lost and then recovered, suppressing the generation of reactive oxygen species. The phenomenon is demonstrated in this video of rodent heart cells. Credit: Yoshihiro Ohta/ TUAT

“Spontaneous fluctuations in mitochondrial membrane potential are physiological phenomena observed in a wide range of cells from plants to mammals,” said Ohta. “In this study, we investigated how this spontaneous fluctuation occurs and what it is useful for.”

The researchers found that increasing the pH of the matrix from neutral to basic significantly increased reactive oxygen species production. They also found that inhibition of the spontaneous fluctuation, or depolarization, increased both the matrix pH and presence of reactive oxygen species.

“Spontaneous transient depolarization may decrease reactive oxygen species production in the mitochondria by inhibiting sustained matrix pH elevation,” Ohta said. “This is the first study suggesting the relationship between spontaneous transient depolarization and reactive oxygen species production.”

While the researchers have not fully elucidated the mechanism by which mitochondria control their reactive oxygen species production, they did propose a model suggesting that spontaneous transient depolarization occurs when increased matrix pH facilitates moving more protons from outside the matrix into the matrix.

The researchers plan to further investigate the mechanism to understand not only how mitochondria can prevent overproduction of reactive oxygen species, but also if detecting the spontaneous fluctuation in mitochondria could indicate the oxidative stress state—and damage—of cells.


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More information:
Jannatul Aklima et al, Effects of Matrix pH on Spontaneous Transient Depolarization and Reactive Oxygen Species Production in Mitochondria, Frontiers in Cell and Developmental Biology (2021). DOI: 10.3389/fcell.2021.692776

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A mitochondrial self-preservation mechanism (2021, July 9)
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