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将具有氧化还原活性的泛醌选择性靶向细胞内的线粒体:抗氧化和抗凋亡特性。

Selective targeting of a redox-active ubiquinone to mitochondria within cells: antioxidant and antiapoptotic properties.

作者信息

Kelso G F, Porteous C M, Coulter C V, Hughes G, Porteous W K, Ledgerwood E C, Smith R A, Murphy M P

机构信息

Departments of Chemistry and Biochemistry, University of Otago, Box 56, Dunedin, New Zealand.

出版信息

J Biol Chem. 2001 Feb 16;276(7):4588-96. doi: 10.1074/jbc.M009093200. Epub 2000 Nov 22.

Abstract

With the recognition of the central role of mitochondria in apoptosis, there is a need to develop specific tools to manipulate mitochondrial function within cells. Here we report on the development of a novel antioxidant that selectively blocks mitochondrial oxidative damage, enabling the roles of mitochondrial oxidative stress in different types of cell death to be inferred. This antioxidant, named mitoQ, is a ubiquinone derivative targeted to mitochondria by covalent attachment to a lipophilic triphenylphosphonium cation through an aliphatic carbon chain. Due to the large mitochondrial membrane potential, the cation was accumulated within mitochondria inside cells, where the ubiquinone moiety inserted into the lipid bilayer and was reduced by the respiratory chain. The ubiquinol derivative thus formed was an effective antioxidant that prevented lipid peroxidation and protected mitochondria from oxidative damage. After detoxifying a reactive oxygen species, the ubiquinol moiety was regenerated by the respiratory chain enabling its antioxidant activity to be recycled. In cell culture studies, the mitochondrially localized antioxidant protected mammalian cells from hydrogen peroxide-induced apoptosis but not from apoptosis induced by staurosporine or tumor necrosis factor-alpha. This was compared with untargeted ubiquinone analogs, which were ineffective in preventing apoptosis. These results suggest that mitochondrial oxidative stress may be a critical step in apoptosis induced by hydrogen peroxide but not for apoptosis induced by staurosporine or tumor necrosis factor-alpha. We have shown that selectively manipulating mitochondrial antioxidant status with targeted and recyclable antioxidants is a feasible approach to investigate the role of mitochondrial oxidative damage in apoptotic cell death. This approach will have further applications in investigating mitochondrial dysfunction in a range of experimental models.

摘要

随着人们认识到线粒体在细胞凋亡中的核心作用,有必要开发特定工具来操控细胞内的线粒体功能。在此,我们报告一种新型抗氧化剂的研发情况,该抗氧化剂能选择性地阻断线粒体氧化损伤,从而推断线粒体氧化应激在不同类型细胞死亡中的作用。这种名为线粒体辅酶Q(mitoQ)的抗氧化剂是一种泛醌衍生物,通过脂肪族碳链与亲脂性三苯基膦阳离子共价连接,从而靶向线粒体。由于线粒体内膜电位较大,阳离子在细胞内的线粒体内积累,泛醌部分插入脂质双层并被呼吸链还原。由此形成的泛醇衍生物是一种有效的抗氧化剂,可防止脂质过氧化并保护线粒体免受氧化损伤。在清除活性氧后,泛醇部分由呼吸链再生,使其抗氧化活性得以循环利用。在细胞培养研究中,这种定位于线粒体的抗氧化剂可保护哺乳动物细胞免受过氧化氢诱导的细胞凋亡,但不能保护其免受星形孢菌素或肿瘤坏死因子-α诱导的细胞凋亡。与之相比,非靶向泛醌类似物在预防细胞凋亡方面无效。这些结果表明,线粒体氧化应激可能是过氧化氢诱导细胞凋亡的关键步骤,但不是星形孢菌素或肿瘤坏死因子-α诱导细胞凋亡的关键步骤。我们已经表明,用靶向且可循环利用的抗氧化剂选择性地操控线粒体抗氧化状态是研究线粒体氧化损伤在凋亡性细胞死亡中作用的一种可行方法。这种方法将在一系列实验模型中进一步应用于研究线粒体功能障碍。

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