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Use of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes (hiPSC-CMs) to Monitor Compound Effects on Cardiac Myocyte Signaling Pathways

机译:使用人类诱导的多能干细胞衍生的心肌细胞(hiPSC-CMs)监测化合物对心肌信号通路的影响

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摘要

There is a need to develop mechanism-based assays to better inform risk of cardiotoxicity. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are gaining rapid acceptance as a biologically relevant in vitro model for use in drug discovery and cardiotoxicity screens. Utilization of hiPSC-CMs for mechanistic investigations would benefit from confirmation of the expression and activity of cellular pathways that are known to regulate cardiac myocyte viability and function. This unit describes an approach to demonstrate the presence and function of signaling pathway(s) in hiPSC-CMs and the effects of treatments on these pathways. We present a workflow that employs protocols to demonstrate protein expression, functional integrity of signaling pathway(s) of interest and that characterize biological consequences of signaling modulation. These protocols utilize a unique combination of structural, functional and biochemical endpoints to interrogate compound effects on cardiomyocytes.
机译:需要开发基于机制的测定法以更好地告知心脏毒性风险。人类诱导的多能干细胞衍生的心肌细胞(hiPSC-CMs)已迅速被接受为生物学上相关的体外模型,用于药物发现和心脏毒性筛查。将hiPSC-CM用于机制研究将受益于确认已知调节心脏心肌细胞活力和功能的细胞途径的表达和活性。本单元描述了一种方法,以证明hiPSC-CM中信号传导途径的存在和功能以及这些途径的治疗效果。我们提出了一个采用协议来证明蛋白质表达,感兴趣的信号通路功能完整性以及表征信号调节生物学后果的工作流程。这些协议利用结构,功能和生化终点的独特组合来询问化合物对心肌细胞的作用。

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