Recording and Interpretation of Active Calcium Transients in Induced Pluripotent Stem Cell-Derived Cardiomyocytes

Maedeh Mozneb, Jemima Moses, Madelyn Arzt, Sean Escopete, Arun Sharma
{"title":"Recording and Interpretation of Active Calcium Transients in Induced Pluripotent Stem Cell-Derived Cardiomyocytes","authors":"Maedeh Mozneb,&nbsp;Jemima Moses,&nbsp;Madelyn Arzt,&nbsp;Sean Escopete,&nbsp;Arun Sharma","doi":"10.1002/cpz1.70030","DOIUrl":null,"url":null,"abstract":"<p>Calcium plays a pivotal role in the excitation-contraction coupling process in cardiomyocytes, a critical multi-parametric event leading to rhythmic contraction. Over the past few decades, calcium signaling in cardiomyocytes has been extensively studied in cardiovascular sciences. However, a standard methodology is needed not only to trace the calcium within cells but also to remove signal processing biases and to accurately interpret the features of calcium transient signals in relation to cardiomyocyte electrophysiology. This article outlines the use of genetically encoded calcium indicator (GCaMP) human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) to record calcium transients. These cells express a green fluorescent signal when calcium binds to intracellular calmodulin, a key regulator of calcium signaling. The extraction and processing of calcium transient waveforms are performed using ImageJ and MATLAB software. Key features of these waveforms are then identified and categorized based on their physiological relevance to cardiomyocyte function. Additionally, this work includes a Support Protocol for the successful replating of cardiomyocytes onto non-traditional culture platforms, such as metallic sensors and polymer-based substrates, to facilitate data multiplexing. The three Basic Protocols outlined here provide a comprehensive approach for maintaining, expanding, and differentiating the GCaMP hiPSCs, video recording of calcium transients, and the subsequent signal extraction, preprocessing, analysis, and data visualization. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Maintenance, expansion, and differentiation of genetically encoded calcium indicator hiPSCs</p><p><b>Support Protocol</b>: Replating GCaMP hiPSC-CMs for stimulation and multielectrode array studies</p><p><b>Basic Protocol 2</b>: Video recording from calcium transients of GCaMP hiPSC-CMs</p><p><b>Basic Protocol 3</b>: Signal extraction, preprocessing, analysis, and data visualization</p>","PeriodicalId":93970,"journal":{"name":"Current protocols","volume":"4 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cpz1.70030","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpz1.70030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Calcium plays a pivotal role in the excitation-contraction coupling process in cardiomyocytes, a critical multi-parametric event leading to rhythmic contraction. Over the past few decades, calcium signaling in cardiomyocytes has been extensively studied in cardiovascular sciences. However, a standard methodology is needed not only to trace the calcium within cells but also to remove signal processing biases and to accurately interpret the features of calcium transient signals in relation to cardiomyocyte electrophysiology. This article outlines the use of genetically encoded calcium indicator (GCaMP) human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) to record calcium transients. These cells express a green fluorescent signal when calcium binds to intracellular calmodulin, a key regulator of calcium signaling. The extraction and processing of calcium transient waveforms are performed using ImageJ and MATLAB software. Key features of these waveforms are then identified and categorized based on their physiological relevance to cardiomyocyte function. Additionally, this work includes a Support Protocol for the successful replating of cardiomyocytes onto non-traditional culture platforms, such as metallic sensors and polymer-based substrates, to facilitate data multiplexing. The three Basic Protocols outlined here provide a comprehensive approach for maintaining, expanding, and differentiating the GCaMP hiPSCs, video recording of calcium transients, and the subsequent signal extraction, preprocessing, analysis, and data visualization. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Maintenance, expansion, and differentiation of genetically encoded calcium indicator hiPSCs

Support Protocol: Replating GCaMP hiPSC-CMs for stimulation and multielectrode array studies

Basic Protocol 2: Video recording from calcium transients of GCaMP hiPSC-CMs

Basic Protocol 3: Signal extraction, preprocessing, analysis, and data visualization

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
记录和解读诱导多能干细胞衍生心肌细胞的活性钙瞬态
钙在心肌细胞的兴奋-收缩耦合过程中发挥着关键作用,这是导致节律性收缩的一个关键的多参数事件。过去几十年来,心血管科学界对心肌细胞中的钙信号进行了广泛研究。然而,不仅需要一种标准方法来追踪细胞内的钙离子,还需要消除信号处理偏差,并准确解释与心肌细胞电生理学相关的钙离子瞬态信号特征。本文概述了利用基因编码钙指示剂(GCaMP)人诱导多能干细胞衍生心肌细胞(hiPSC-CMs)记录钙瞬态的方法。当钙与细胞内钙调蛋白结合时,这些细胞会发出绿色荧光信号,钙调蛋白是钙信号转导的关键调节因子。钙离子瞬态波形的提取和处理使用 ImageJ 和 MATLAB 软件。然后根据这些波形与心肌细胞功能的生理相关性对其关键特征进行识别和分类。此外,这项工作还包括一项支持协议,用于将心肌细胞成功复制到非传统培养平台(如金属传感器和聚合物基底)上,以促进数据复用。本文概述的三项基本规程为 GCaMP hiPSCs 的维护、扩增和分化、钙离子瞬态视频记录以及后续的信号提取、预处理、分析和数据可视化提供了全面的方法。© 2024 作者。当前协议》由 Wiley Periodicals LLC 出版。基本方案 1:基因编码钙离子指示剂 hiPSCs 的维持、扩增和分化 支持方案:基本方案 2:GCaMP hiPSC-CMs 的钙离子瞬态视频记录 基本方案 3:信号提取、预处理、分析和数据可视化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
4.00
自引率
0.00%
发文量
0
期刊最新文献
Analysis of Free Oligosaccharides in Urine by High-Performance Liquid Chromatography–Tandem Mass Spectrometry Synthesis and Application of a Caged Bioluminescent Probe for the Immunoproteasome Engineering and Evaluating Vascularized Organotypic Spheroids On-Chip Vesicular Stomatitis Virus as a Platform for Protease Activity Measurements Workflow to Select Functional Promoter DNA Baits and Screen Arrayed Gene Libraries in Yeast
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1