Mitochondrial Management of Reactive Oxygen Species

  • Gaetana Napolitano
    Dipartimento di Scienze e Tecnologie, Università degli Studi di Napoli Parthenope, Via Acton, 80133 Naples, Italy
  • Gianluca Fasciolo
    Dipartimento di Biologia, Università di Napoli Federico II, Complesso Universitario Monte Sant’Angelo, Via Cinthia, 80126 Naples, Italy
  • Paola Venditti
    Dipartimento di Biologia, Università di Napoli Federico II, Complesso Universitario Monte Sant’Angelo, Via Cinthia, 80126 Naples, Italy

説明

<jats:p>Mitochondria in aerobic eukaryotic cells are both the site of energy production and the formation of harmful species, such as radicals and other reactive oxygen species, known as ROS. They contain an efficient antioxidant system, including low-molecular-mass molecules and enzymes that specialize in removing various types of ROS or repairing the oxidative damage of biological molecules. Under normal conditions, ROS production is low, and mitochondria, which are their primary target, are slightly damaged in a similar way to other cellular compartments, since the ROS released by the mitochondria into the cytosol are negligible. As the mitochondrial generation of ROS increases, they can deactivate components of the respiratory chain and enzymes of the Krebs cycle, and mitochondria release a high amount of ROS that damage cellular structures. More recently, the feature of the mitochondrial antioxidant system, which does not specifically deal with intramitochondrial ROS, was discovered. Indeed, the mitochondrial antioxidant system detoxifies exogenous ROS species at the expense of reducing the equivalents generated in mitochondria. Thus, mitochondria are also a sink of ROS. These observations highlight the importance of the mitochondrial antioxidant system, which should be considered in our understanding of ROS-regulated processes. These processes include cell signaling and the progression of metabolic and neurodegenerative disease.</jats:p>

収録刊行物

  • Antioxidants

    Antioxidants 10 (11), 1824-, 2021-11-17

    MDPI AG

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