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The role of mammalian cardiac t-tubules in excitation-contraction coupling: experimental and computational approaches.哺乳动物心脏横小管在兴奋-收缩偶联中的作用:实验与计算方法
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心肌细胞中线粒体的时空振荡揭示了同步线粒体簇的调制。

Spatio-temporal oscillations of individual mitochondria in cardiac myocytes reveal modulation of synchronized mitochondrial clusters.

机构信息

Charité Universitätsmedizin Berlin, Campus Virchow-Klinikum, Med. Klinik m. S. Kardiologie, Berlin 13353, Germany.

出版信息

Proc Natl Acad Sci U S A. 2010 Aug 10;107(32):14315-20. doi: 10.1073/pnas.1007562107. Epub 2010 Jul 23.

DOI:10.1073/pnas.1007562107
PMID:20656937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2922526/
Abstract

Mitochondrial networks in cardiac myocytes under oxidative stress show collective (cluster) behavior through synchronization of their inner membrane potentials (DeltaPsi(m)). However, it is unclear whether the oscillation frequency and coupling strength between individual mitochondria affect the size of the cluster and vice versa. We used the wavelet transform and developed advanced signal processing tools that allowed us to capture individual mitochondrial DeltaPsi(m) oscillations in cardiac myocytes and examine their dynamic spatio-temporal properties. Heterogeneous frequency behavior prompted us to sort mitochondria according to their frequencies. Signal analysis of the mitochondrial network showed an inverse relationship between cluster size and cluster frequency as well as between cluster amplitude and cluster size. High cross-correlation coefficients between neighboring mitochondria clustered longitudinally along the myocyte striations, indicated anisotropic communication between mitochondria. Isochronal mapping of the onset of myocyte-wide DeltaPsi(m) depolarization further exemplified heterogeneous DeltaPsi(m) among mitochondria. Taken together, the results suggest that frequency and amplitude modulation of clusters of synchronized mitochondria arises by means of strong changes in local coupling between neighboring mitochondria.

摘要

在氧化应激下,心肌细胞中的线粒体网络通过其内膜电位(DeltaPsi(m))的同步显示出集体(簇)行为。然而,目前尚不清楚单个线粒体之间的振荡频率和耦合强度是否会影响簇的大小,反之亦然。我们使用了小波变换并开发了先进的信号处理工具,使我们能够捕捉心肌细胞中单个线粒体 DeltaPsi(m) 的振荡,并检查它们的动态时空特性。异质的频率行为促使我们根据频率对线粒体进行分类。线粒体网络的信号分析表明,簇大小和簇频率之间以及簇幅度和簇大小之间呈负相关关系。沿着心肌条纹纵向聚类的相邻线粒体之间具有较高的互相关系数,表明线粒体之间存在各向异性的通讯。心肌细胞全范围 DeltaPsi(m) 去极化起始的等时映射进一步说明了线粒体之间存在异质的 DeltaPsi(m)。总之,研究结果表明,同步线粒体簇的频率和幅度调制是通过相邻线粒体之间局部耦合的强烈变化产生的。