| Literature DB >> 29364522 |
Arun Sharma1, Christopher N Toepfer1,2, Manuel Schmid1,3, Amanda C Garfinkel1, Christine E Seidman1,4.
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.Entities:
Keywords: CRISPR; cardiomyocytes; contractility; drug screening; fluorescent reporter; iPSCs; pluripotent stem cells; sarcomere
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Year: 2018 PMID: 29364522 PMCID: PMC5786381 DOI: 10.1002/cphg.53
Source DB: PubMed Journal: Curr Protoc Hum Genet ISSN: 1934-8258