Institute for Molecular Cell Biology, Center for Molecular Signaling (PZMS), Medical Faculty, Saarland University, Homburg, Germany.
Elife. 2017 Nov 14;6:e30425. doi: 10.7554/eLife.30425.
In beating cardiomyocytes, synchronized localized Ca transients from thousands of active excitation-contraction coupling sites (ECC couplons) comprising plasma and sarcoplasmic reticulum membrane calcium channels are important determinants of the heart's performance. Nevertheless, our knowledge about the properties of ECC couplons is limited by the lack of appropriate experimental and analysis strategies. We designed CaCLEAN to untangle the fundamental characteristics of ECC couplons by combining the astronomer's CLEAN algorithm with known properties of calcium diffusion. CaCLEAN empowers the investigation of fundamental properties of ECC couplons in beating cardiomyocytes without pharmacological interventions. Upon examining individual ECC couplons at the nanoscopic level, we reveal their roles in the negative amplitude-frequency relationship and in β-adrenergic stimulation, including decreasing and increasing firing reliability, respectively. CaCLEAN combined with 3D confocal imaging of beating cardiomyocytes provides a functional 3D map of active ECC couplons (on average, 17,000 per myocyte). CaCLEAN will further enlighten the ECC-couplon-remodelling processes that underlie cardiac diseases.
在跳动的心肌细胞中,来自数千个活跃的兴奋-收缩偶联(ECC 偶联)位点的同步局部钙瞬变,这些位点包括质膜和肌浆网钙通道,是心脏功能的重要决定因素。然而,由于缺乏适当的实验和分析策略,我们对 ECC 偶联的特性的了解是有限的。我们设计了 CaCLEAN,通过将天文学家的 CLEAN 算法与钙扩散的已知特性相结合,来梳理 ECC 偶联的基本特性。CaCLEAN 可以在不进行药理学干预的情况下,研究跳动心肌细胞中 ECC 偶联的基本特性。通过在纳米尺度上检查单个 ECC 偶联,我们揭示了它们在负幅度-频率关系和β-肾上腺素能刺激中的作用,分别是降低和增加发射可靠性。CaCLEAN 结合 3D 共聚焦成像跳动的心肌细胞,提供了活性 ECC 偶联的功能 3D 图谱(每个心肌细胞平均 17000 个)。CaCLEAN 将进一步阐明心脏疾病的基础 ECC 偶联重塑过程。