Zhang Xuemeng, Kampourakis Thomas, Yan Ziqian, Sevrieva Ivanka, Irving Malcolm, Sun Yin-Biao
Randall Division of Cell and Molecular Biophysics, King's College London, London, United Kingdom.
British Heart Foundation Centre of Research Excellence, King's College London, London, United Kingdom.
Elife. 2017 Feb 23;6:e24081. doi: 10.7554/eLife.24081.
The Frank-Starling relation is a fundamental auto-regulatory property of the heart that ensures the volume of blood ejected in each heartbeat is matched to the extent of venous filling. At the cellular level, heart muscle cells generate higher force when stretched, but despite intense efforts the underlying molecular mechanism remains unknown. We applied a fluorescence-based method, which reports structural changes separately in the thick and thin filaments of rat cardiac muscle, to elucidate that mechanism. The distinct structural changes of troponin C in the thin filaments and myosin regulatory light chain in the thick filaments allowed us to identify two aspects of the Frank-Starling relation. Our results show that the enhanced force observed when heart muscle cells are maximally activated by calcium is due to a change in filament structure, but the increase in calcium sensitivity at lower calcium levels is due to a change in filament structure.
弗兰克 - 斯塔林关系是心脏的一种基本自动调节特性,可确保每次心跳射出的血量与静脉充盈程度相匹配。在细胞水平上,心肌细胞在被拉伸时会产生更大的力量,但尽管进行了深入研究,其潜在的分子机制仍然未知。我们应用了一种基于荧光的方法,该方法分别报告大鼠心肌粗肌丝和细肌丝的结构变化,以阐明该机制。细肌丝中的肌钙蛋白C和粗肌丝中的肌球蛋白调节轻链的明显结构变化使我们能够确定弗兰克 - 斯塔林关系的两个方面。我们的结果表明,当心肌细胞被钙最大程度激活时观察到的力量增强是由于细丝结构的变化,而在较低钙水平下钙敏感性的增加是由于细丝结构的变化。