Teh Irvin, Burton Rebecca A B, McClymont Darryl, Capel Rebecca A, Aston Daniel, Kohl Peter, Schneider Jürgen E
Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Department of Pharmacology, University of Oxford, Oxford, United Kingdom.
Prog Biophys Mol Biol. 2016 Jul;121(2):85-96. doi: 10.1016/j.pbiomolbio.2016.06.001. Epub 2016 Jun 16.
Myocardial microstructure and its macroscopic materialisation are fundamental to the function of the heart. Despite this importance, characterisation of cellular features at the organ level remains challenging, and a unifying description of the structure of the heart is still outstanding. Here, we optimised diffusion tensor imaging data to acquire high quality data in ex vivo rabbit hearts in slack and contractured states, approximating diastolic and systolic conditions. The data were analysed with a suite of methods that focused on different aspects of the myocardium. In the slack heart, we observed a similar transmural gradient in helix angle of the primary eigenvector of up to 23.6°/mm in the left ventricle and 24.2°/mm in the right ventricle. In the contractured heart, the same transmural gradient remained largely linear, but was offset by up to +49.9° in the left ventricle. In the right ventricle, there was an increase in the transmural gradient to 31.2°/mm and an offset of up to +39.0°. The application of tractography based on each eigenvector enabled visualisation of streamlines that depict cardiomyocyte and sheetlet organisation over large distances. We observed multiple V- and N-shaped sheetlet arrangements throughout the myocardium, and insertion of sheetlets at the intersection of the left and right ventricle. This study integrates several complementary techniques to visualise and quantify the heart's microstructure, projecting parameter representations across different length scales. This represents a step towards a more comprehensive characterisation of myocardial microstructure at the whole organ level.
心肌微观结构及其宏观表现形式对心脏功能至关重要。尽管其重要性不言而喻,但在器官层面表征细胞特征仍具有挑战性,对心脏结构的统一描述也尚未完成。在此,我们优化了扩散张量成像数据,以获取处于松弛和收缩状态的离体兔心脏的高质量数据,分别近似舒张期和收缩期情况。使用了一系列专注于心肌不同方面的方法对数据进行分析。在松弛的心脏中,我们观察到在左心室中主特征向量的螺旋角存在类似的透壁梯度,高达23.6°/mm,在右心室中为24.2°/mm。在收缩的心脏中,相同的透壁梯度在很大程度上仍保持线性,但在左心室中偏移了高达 +49.9°。在右心室中,透壁梯度增加到31.2°/mm,偏移高达 +39.0°。基于每个特征向量应用纤维束成像能够可视化描绘远距离心肌细胞和薄片组织的流线。我们在整个心肌中观察到多个V形和N形薄片排列,以及薄片在左心室和右心室交界处的插入。本研究整合了多种互补技术,以可视化和量化心脏的微观结构,在不同长度尺度上投影参数表示。这代表了朝着在整个器官层面更全面地表征心肌微观结构迈出的一步。