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Cardiolipin fatty acid remodeling regulates mitochondrial function by modifying the electron entry point in the respiratory chain

机译:心磷脂脂肪酸重塑通过修饰呼吸链中的电子进入点来调节线粒体功能

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Modifications of cardiolipin (CL) levels or compositions are associated with changes in mitochondrial function in a wide range of pathologies. We have made the discovery that acetaminophen remodels CL fatty acids composition from tetralinoleoyl to linoleoyltrioleoyl-CL, a remodeling that is associated with decreased mitochondrial respiration. Our data show that CL remodeling causes a shift in electron entry from complex II to the beta-oxidation electron transfer flavoprotein quinone oxidoreductase (ETF/QOR) pathway. These data demonstrate that electron entry in the respiratory chain is regulated by CL fatty acid composition and provide proof-of concept that pharmacological intervention can be used to modify CL composition. (C) 2016 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
机译:在多种病理中,心磷脂(CL)水平或组成的改变与线粒体功能的变化有关。我们已经发现对乙酰氨基酚可以将CL脂肪酸的组成从四亚油酰基重塑为亚油酰基三油酰-CL,这种重塑与线粒体呼吸减少有关。我们的数据表明,CL重塑导致电子从复合物II进入β-氧化电子转移黄素蛋白醌氧化还原酶(ETF / QOR)途径的转变。这些数据表明电子进入呼吸链受CL脂肪酸组成的调节,并提供了药理干预可用于修改CL组成的概念证明。 (C)2016 Elsevier B.V.和线粒体研究学会。版权所有。

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