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Generation and Analysis of Pluripotent Stem Cell-Derived Cardiomyocytes and Endothelial Cells for High Content Screening Purposes
Author(s) -
Tünde Berecz,
M Husveth-Toth,
Maxime Mioulane,
Béla Merkely,
Àgota Apàti,
Gábor Földes
Publication year - 2019
Publication title -
methods in molecular biology
Language(s) - English
Resource type - Book series
SCImago Journal Rank - 0.711
H-Index - 152
eISSN - 1940-6029
pISSN - 1064-3745
DOI - 10.1007/7651_2019_222
Subject(s) - induced pluripotent stem cell , high content screening , drug discovery , microbiology and biotechnology , cell type , human induced pluripotent stem cells , in vitro , computational biology , cell , biology , endothelial stem cell , phenotypic screening , phenotype , cell culture , embryonic stem cell , bioinformatics , gene , biochemistry , genetics
Human-induced pluripotent stem cells (hiPSCs) and their differentiated derivatives became a new, promising source for in vitro screening techniques. Cell lines derived from healthy individuals can be applied for drug safety testing, while patient-derived cells provide a platform to model diseases in vitro and can be used as a tool for personalized medicine including specific drug efficacy testing and identification of new pharmacological targets as well as for tailoring pharmacological therapies. Efficient differentiation protocols yielding cardiomyocytes or endothelial cells derived from iPSCs have been developed recently. Phenotypic characterization and gene expression profiling of these derivatives can reveal clues for developmental and pathological questions. Moreover, functional analysis and cell-based assays using automated fluorescence imaging platform and high content analysis characterize cell type-specific profiles of hiPSC-derived cardiomyocytes (hiPSC-CM) and endothelial cells (hiPSC-EC) at the cellular and subcellular levels. This can be utilized in a platform which can provide multiple endpoint profiles of candidate compounds.

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