Spatiotemporal Quantification of In Vitro Cardiomyocyte Contraction Dynamics Using Video Microscopy-based Software Tool

A. Ahola, J. Hyttinen
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Abstract

Stem cell derived cardiomyocytes provide a platform for a variety of studies. The typically performed electrophysiological measurements do not describe the primary function of these cells, contraction and its biomechanics. Video microscopy-based analysis of motion has become a feasible option for these studies. Here, we demonstrate methods for spatiotemporal quantification of stem cell derived cardiomyocytes, implemented in an in-house developed MATLAB-based software tool. The tool is capable of characterizing cardiomyocyte contraction with minimal user bias. The results show that automatic segmentation using a power spectral density -based measure enables segmentation based on contractile function. Further, based on segmented boundaries, we introduce automatically calculated parameters for quantification the contractile function and its propagation through the cell culture based on timings of different contraction phases. The methods presented here form a basis for quantifying and understanding the contraction dynamics and the propagation of contraction in cultures involving cardiomyocytes.
利用基于视频显微镜的软件工具对体外心肌细胞收缩动力学进行时空量化
干细胞衍生的心肌细胞为各种研究提供了一个平台。通常进行的电生理测量不能描述这些细胞的主要功能、收缩及其生物力学。基于视频显微镜的运动分析已经成为这些研究的可行选择。在这里,我们展示了干细胞来源的心肌细胞的时空量化方法,在内部开发的基于matlab的软件工具中实现。该工具能够以最小的用户偏差表征心肌细胞收缩。结果表明,基于功率谱密度的自动分割能够实现基于收缩函数的分割。此外,在分割边界的基础上,我们引入了自动计算的参数来量化收缩功能,并根据不同收缩阶段的时间在细胞培养中传播。本文提出的方法为量化和理解心肌细胞在培养过程中的收缩动力学和收缩增殖奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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