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Subsarcolemmal mitochondrial flashes induced by hypochlorite stimulation in cardiac myocytes

机译:次氯酸盐刺激心肌细胞引起的肌膜下线粒体闪烁

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Mitochondrial superoxide flash (mitoflash) reflects quantal and bursting superoxide production and concurrent membrane depolarization triggered by transient mitochondrial permeability transition in many types of cells, at the level of single mitochondria. Here we investigate reactive oxygen species (ROS)-mediated modulation of mitoflash activity in cardiac myocytes and report a surprising finding that hypochlorite ions potently and preferentially triggered mitoflashes in the subsarcolemmal mitochondria (SSM), whereas hydrogen peroxide (H2O2) elicited mitoflash activity uniformly among SSM and interfibrillar mitochondria (IFM). The striking SSM mitoflash response to hypochlorite stimulation remained intact in cardiac myocytes from NOX2-deficient mice, excluding local NOX2-mediated ROS as the major player. Furthermore, it occurred concomitantly with SSM Ca2+ accumulation and local Ca2+ and CaMKII signaling played an important modulatory role by altering frequency and unitary properties of SSM mitoflashes. These findings underscore the functional heterogeneity of SSM and IFM and the oxidant-specific responsiveness of mitochondria to ROS, and may bear important ramifications in devising therapeutic strategies for the treatment of oxidative stress-related heart diseases.
机译:线粒体过氧化物闪光(mitoflash)反映了许多类型细胞在单个线粒体水平上由瞬时线粒体通透性转变触发的定量和爆发性超氧化物生成以及同时发生的膜去极化。在这里,我们研究了活性氧(ROS)介导的心肌细胞线粒体闪动的调节,并报告了一个令人惊讶的发现:次氯酸盐离子有效地并优先触发了结膜下线粒体(SSM)中的线粒体闪动,而过氧化氢(H2O2)均匀地引起线粒体闪动活性。 SSM和原纤维间线粒体(IFM)。对次氯酸盐刺激的惊人SSM线粒体闪现反应在来自NOX2缺陷小鼠的心肌细胞中保持完整,但不包括主要由NOX2介导的ROS。此外,它与SSM Ca2 +积累同时发生,局部Ca2 +和CaMKII信号传导通过改变SSM线粒体闪光的频率和单位特性发挥重要的调节作用。这些发现强调了SSM和IFM的功能异质性以及线粒体对ROS的氧化剂特异性反应性,并且在设计用于治疗与氧化应激相关的心脏病的治疗策略中可能具有重要意义。

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