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Automated, Non-Invasive Characterization of Stem Cell-Derived Cardiomyocytes from Phase-Contrast Microscopy

机译:从相差显微镜对干细胞衍生的心肌细胞的自动化,非侵入性表征

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Stem cell-derived cardiomyocytes hold tremendous potential for drug development and safety testing related to cardiovascular health. The characterization of cardiomyocytes is most commonly performed using electrophysiological systems, which are expensive, laborious to use, and may induce undesirable cellular response. Here, we present a new method for non-invasive characterization of cardiomyocytes using video microscopy and image analysis. We describe an automated pipeline that consists of segmentation of beating regions, robust beating signal calculation, signal quantification and modeling, and hierarchical clustering. Unlike previous imaging-based methods, our approach enables clinical applications by capturing beating patterns and arrhythmias across healthy and diseased cells with varied densities. We demonstrate the strengths of our algorithm by characterizing the effects of two commercial drugs known to modulate beating frequency and irregularity. Our results provide, to our knowledge, the first clinically-relevant demonstration of a fully-automated and non-invasive imaging-based beating assay for characterization of stem cell-derived cardiomyocytes.
机译:干细胞衍生的心肌细胞具有与心血管健康相关的药物开发和安全性测试的巨大潜力。心肌细胞的表征最通常是使用电生理系统进行的,该系统昂贵,使用费力并且可能引起不良的细胞反应。在这里,我们介绍了一种使用视频显微镜和图像分析对心肌细胞进行非侵入性表征的新方法。我们描述了一种自动流水线,该流水线包括跳动区域的分段,强大的跳动信号计算,信号量化和建模以及分层聚类。与以前的基于成像的方法不同,我们的方法通过捕获各种密度的健康和患病细胞的跳动模式和心律不齐来实现临床应用。我们通过表征两种已知可调节跳动频率和不规则性的商业药物的作用,证明了我们算法的优势。就我们所知,我们的结果提供了首次临床相关的证明,该技术基于全自动,非侵入性成像的搏动测定用于表征干细胞衍生的心肌细胞。

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