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绿色荧光蛋白标记肌节报告基因的人诱导多能干细胞衍生心肌细胞的分化与收缩性分析

Differentiation and Contractile Analysis of GFP-Sarcomere Reporter hiPSC-Cardiomyocytes.

作者信息

Sharma Arun, Toepfer Christopher N, Schmid Manuel, Garfinkel Amanda C, Seidman Christine E

机构信息

Department of Genetics, Harvard Medical School, Boston, Massachusetts.

Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.

出版信息

Curr Protoc Hum Genet. 2018 Jan 24;96:21.12.1-21.12.12. doi: 10.1002/cphg.53.

Abstract

Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) represent a powerful cellular platform for illuminating mechanisms of human cardiovascular disease and for pharmacological screening. Recent advances in CRISPR/Cas9-mediated genome editing technology underlie this profound utility. We have generated hiPSC-CMs harboring fluorescently-tagged sarcomeric proteins, which provide a tool to non-invasively study human sarcomere function and dysfunction. In this unit, we illustrate methods for conducting high-efficiency, small molecule-mediated differentiation of hiPSCs into cardiomyocytes, and for performing non-invasive contractile analysis through direct sarcomere tracking of GFP-sarcomere reporter hiPSC-CMs. We believe that this type of analysis can overcome sensitivity problems found in other forms of contractile assays involving hiPSC-CMs by directly measuring contractility at the fundamental contractile unit of the hiPSC-CM, the sarcomere. © 2018 by John Wiley & Sons, Inc.

摘要

人诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)是用于阐明人类心血管疾病机制和进行药物筛选的强大细胞平台。CRISPR/Cas9介导的基因组编辑技术的最新进展是这种巨大效用的基础。我们已经生成了带有荧光标记肌节蛋白的hiPSC-CMs,这为非侵入性研究人类肌节功能和功能障碍提供了一种工具。在本单元中,我们阐述了将hiPSC高效、小分子介导分化为心肌细胞的方法,以及通过对GFP-肌节报告基因hiPSC-CMs进行直接肌节追踪来进行非侵入性收缩分析的方法。我们相信,这种类型的分析可以通过在hiPSC-CM的基本收缩单位——肌节处直接测量收缩力,克服在涉及hiPSC-CMs的其他形式收缩测定中发现的灵敏度问题。© 2018约翰威立父子出版公司

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ed/5786381/56114217f659/nihms911231f1.jpg

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