Departments of Mechanical Engineering & Bioengineering, Stanford University, CA, USA.
California Medical Innovations Institute, Inc., San Diego, CA, USA.
Acta Biomater. 2019 Mar 1;86:66-76. doi: 10.1016/j.actbio.2018.12.053. Epub 2019 Jan 7.
Dilated cardiomyopathy is a progressive irreversible disease associated with contractile dysfunction and heart failure. During dilated cardiomyopathy, elevated diastolic wall strains trigger mechanotransduction pathways that initiate the addition of sarcomeres in series and an overall increase in myocyte length. At the whole organ level, this results in a chronic dilation of the ventricles, an increase in end diastolic and end systolic volumes, and a decrease in ejection fraction. However, how exactly changes in sarcomere number translate into changes in myocyte morphology, and how these cellular changes translate into ventricular dilation remains incompletely understood. Here we combined a chronic animal study, continuum growth modeling, and machine learning to quantify correlations between sarcomere dynamics, myocyte morphology, and ventricular dilation. In an eight-week long volume overload study of six pigs, we found that the average sarcomere number increased by +3.8%/week, from 47 to 62, resulting in a myocyte lengthening of +3.3%/week, from 85 to 108 μm, while the sarcomere length and myocyte width remained unchanged. At the same time, the average end diastolic volume increased by +6.0%/week. Using continuum growth modeling and Bayesian inference, we correlated alterations on the subcellular, cellular, and organ scales and found that the serial sarcomere number explained 88% of myocyte lengthening, which, in turn, explained 54% of cardiac dilation. Our results demonstrate that sarcomere number and myocyte length are closely correlated and constitute the major determinants of dilated heart failure. We anticipate our study to be a starting point for more sophisticated multiscale models of heart failure. Our study suggests that altering sarcomere turnover-and with it myocyte morphology and ventricular dimensions-could be a potential therapeutic target to attenuate or reverse the progression of heart failure. STATEMENT OF SIGNIFICANCE: Heart failure is a significant global health problem that affects more than 25 million people worldwide and increases in prevalence as the population ages. Heart failure has been studied excessively at various scales; yet, there is no compelling concept to connect knowledge from the subcellular, cellular, and organ level across the scales. Here we combined a chronic animal study, continuum growth modeling, and machine learning to quantify correlations between sarcomere dynamics, myocyte morphology, and ventricular dilation. We found that the serial sarcomere number explained 88% of myocyte lengthening, which, in turn, explained 54% of cardiac dilation. Our results show that sarcomere number and myocyte length are closely correlated and constitute the major determinants of dilated heart failure. This suggests that altering the sarcomere turnover-and with it myocyte morphology and ventricular dimensions-could be a potential therapeutic target to attenuate or reverse heart failure.
扩张型心肌病是一种进行性、不可逆的疾病,与收缩功能障碍和心力衰竭有关。在扩张型心肌病中,升高的舒张壁应变引发机械转导途径,导致肌节串联增加,心肌细胞长度总体增加。在整个器官水平上,这会导致心室慢性扩张、舒张末期和收缩末期容积增加以及射血分数降低。然而,肌节数量的变化如何精确转化为心肌细胞形态的变化,以及这些细胞变化如何转化为心室扩张,仍不完全清楚。在这里,我们结合了一项慢性动物研究、连续体生长模型和机器学习,以量化肌节动力学、心肌细胞形态和心室扩张之间的相关性。在一项为期八周的六头猪容量超负荷研究中,我们发现平均肌节数量每周增加+3.8%,从 47 个增加到 62 个,导致心肌细胞长度每周增加+3.3%,从 85 微米增加到 108 微米,而肌节长度和心肌细胞宽度保持不变。同时,平均舒张末期容积每周增加+6.0%。使用连续体生长模型和贝叶斯推断,我们对亚细胞、细胞和器官尺度上的变化进行了相关分析,发现串联肌节数量解释了心肌细胞伸长的 88%,而心肌细胞伸长又解释了心脏扩张的 54%。我们的研究结果表明,肌节数量和心肌细胞长度密切相关,是扩张性心力衰竭的主要决定因素。我们预计我们的研究将成为心力衰竭更复杂的多尺度模型的起点。我们的研究表明,改变肌节周转率——随之改变心肌细胞形态和心室尺寸——可能是减轻或逆转心力衰竭进展的潜在治疗靶点。
心力衰竭是一个重大的全球健康问题,影响着全球超过 2500 万人,并且随着人口老龄化而增加。心力衰竭已经在各个尺度上进行了过度研究;然而,没有一个引人注目的概念可以将亚细胞、细胞和器官水平的知识联系起来。在这里,我们结合了一项慢性动物研究、连续体生长模型和机器学习,以量化肌节动力学、心肌细胞形态和心室扩张之间的相关性。我们发现串联肌节数量解释了心肌细胞伸长的 88%,而心肌细胞伸长又解释了心脏扩张的 54%。我们的研究结果表明,肌节数量和心肌细胞长度密切相关,是扩张性心力衰竭的主要决定因素。这表明改变肌节周转率——随之改变心肌细胞形态和心室尺寸——可能是减轻或逆转心力衰竭的潜在治疗靶点。