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Identification and characterization of embryonic stem cell‐derived pacemaker and atrial cardiomyocytes
Author(s) -
Kolossov Eugen,
Lu Zhongju,
Drobinskaya Irina,
Gassanov Natig,
Duan Yaqi,
Sauer Heinrich,
Manzke Oliver,
Bloch Wilhelm,
Bohlen Heribert,
Hescheler Jürgen,
Fleischmann Bernd K.
Publication year - 2005
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.03-1451fje
Subject(s) - green fluorescent protein , embryonic stem cell , embryoid body , flow cytometry , biology , myh6 , myosin , microbiology and biotechnology , pacemaker potential , patch clamp , chemistry , myosin light chain kinase , gene , electrophysiology , neuroscience , genetics , adult stem cell , myh7
The aim of this study was to identify and functionally characterize cardiac subtypes during early stages of development. For this purpose, transgenic embryonic stem cells were generated using the α‐myosin heavy chain promoter driving the expression of the enhanced green fluorescent protein (EGFP). EGFP‐positive clusters of cells were first observed as early as 7 days of development, thus, even before the initiation of the contractile activity. Flow cytometry and single‐cell fluorescence measurements evidenced large diversities of EGFP intensity. Patch‐clamp experiments showed EGFP expression exclusively in pacemaker and atrial but not ventricular cells. The highest fluorescence intensities were detected in pacemaker‐like cardiomyocytes. In accordance, multielectrode‐array recordings of whole embryoid bodies confirmed that the pacemaker center coincided with strongly EGFP‐positive areas. The cardiac subtypes displayed already at this early stage differential characteristics of electrical activity and ion channel expression. Thus, quantitation of the α‐myosin heavy chain driven reporter gene expression allows identification and functional characterization of early cardiac subtypes.
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