{"title":"Use of Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes (hiPSC-CMs) to Monitor Compound Effects on Cardiac Myocyte Signaling Pathways","authors":"Liang Guo, Sandy Eldridge, Mike Furniss, Jodie Mussio, Myrtle Davis","doi":"10.1002/9780470559277.ch150035","DOIUrl":null,"url":null,"abstract":"<p>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 rapidly gaining 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 pathways in hiPSC-CMs and the effects of treatments on these pathways. We present a workflow that employs protocols to demonstrate protein expression and functional integrity of signaling pathway(s) of interest and to characterize biological consequences of signaling modulation. These protocols utilize a unique combination of structural, functional, and biochemical endpoints to interrogate compound effects on cardiomyocytes. © 2015 by John Wiley & Sons, Inc.</p>","PeriodicalId":38051,"journal":{"name":"Current protocols in chemical biology","volume":"7 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/9780470559277.ch150035","citationCount":"25","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/9780470559277.ch150035","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 25
Abstract
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 rapidly gaining 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 pathways in hiPSC-CMs and the effects of treatments on these pathways. We present a workflow that employs protocols to demonstrate protein expression and functional integrity of signaling pathway(s) of interest and to characterize biological consequences of signaling modulation. These protocols utilize a unique combination of structural, functional, and biochemical endpoints to interrogate compound effects on cardiomyocytes. © 2015 by John Wiley & Sons, Inc.
利用人诱导多能干细胞衍生心肌细胞(hiPSC-CMs)监测心肌细胞信号通路的复合效应
有必要开发基于机制的分析,以更好地了解心脏毒性的风险。人类诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)作为一种生物相关的体外模型正在迅速被接受,用于药物发现和心脏毒性筛选。利用hiPSC-CMs进行机制研究将有利于确认已知调节心肌细胞活力和功能的细胞通路的表达和活性。本单元描述了一种方法来证明hiPSC-CMs中信号通路的存在和功能以及治疗对这些通路的影响。我们提出了一个工作流,该工作流采用协议来证明感兴趣的信号通路的蛋白质表达和功能完整性,并表征信号调节的生物学后果。这些方案利用结构、功能和生化终点的独特组合来询问对心肌细胞的复合效应。©2015 by John Wiley &儿子,Inc。
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