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Cyclophilin D-dependent mitochondrial permeability transition regulates some necrotic but not apoptotic cell death

机译:亲环蛋白D依赖的线粒体通透性转变调节某些坏死细胞但不凋亡

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Mitochondria play an important role in energy production, Ca~(2+) homeostasis and cell death. In recent years, the role of the mitochondria in apoptotic and necrotic cell death has attracted much attention. In apoptosis and necrosis, the mitochondrial permeability transition (mPT), which leads to disruption of the mitochondrial membranes and mitochondrial dysfunction, is considered to be one of the key events, although its exact role in cell death remains elusive. We therefore created mice lacking cyclophilin D (CypD), a protein considered to be involved in the mPT, to analyse its role in cell death. CypD-deficient mice were developmentally normal and showed no apparent anomalies, but CypD-deficient mitochondria did not undergo the cyclosporin A-sensitive mPT. CypD-deficient cells died normally in response to various apoptotic stimuli, but showed resistance to necrotic cell death induced by reactive oxygen species and Ca~(2+) overload. In addition, CypD-deficient mice showed a high level of resistance to ischaemia/reperfusion-induced cardiac injury. Our results indicate that the CypD-dependent mPT regulates some forms of necrotic death, but not apoptotic death.
机译:线粒体在能量产生,Ca〜(2+)稳态和细胞死亡中起重要作用。近年来,线粒体在凋亡和坏死细胞死亡中的作用引起了广泛关注。在细胞凋亡和坏死中,导致线粒体膜破裂和线粒体功能障碍的线粒体通透性转变(mPT)被认为是关键事件之一,尽管其在细胞死亡中的确切作用仍然难以捉摸。因此,我们创建了缺乏亲环蛋白D(CypD)的小鼠来分析其在细胞死亡中的作用,亲环蛋白D(CypD)被认为与mPT有关。 CypD缺陷小鼠发育正常,没有明显异常,但CypD缺陷线粒体未经历环孢菌素A敏感性mPT。 CypD缺陷细胞可响应各种凋亡刺激而正常死亡,但对活性氧和Ca〜(2+)超负荷诱导的坏死细胞死亡具有抵抗力。此外,CypD缺陷型小鼠对缺血/再灌注诱导的心脏损伤显示出高水平的抵抗力。我们的结果表明,依赖CypD的mPT调节某些形式的坏死性死亡,而不是凋亡性死亡。

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