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Myogenic differentiation in atrium‐derived adult cardiac pluripotent cells and the transcriptional regulation of GATA4 and myogenin on ANP promoter
Author(s) -
Kamrul Hasan Md,
Komoike Yuta,
Tsunesumi Shinichiro,
Nakao Ryota,
Nagao Hiroaki,
Matsuoka Rumiko,
Kawaguchi Nanako
Publication year - 2010
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1111/j.1365-2443.2010.01394.x
Subject(s) - myogenin , biology , gata4 , myogenesis , myocyte , transcription factor , induced pluripotent stem cell , microbiology and biotechnology , chromatin immunoprecipitation , myf5 , promoter , gene expression , embryonic stem cell , gene , biochemistry
We established cardiac pluripotent stem‐like cells from the left atrium (LA‐PCs) of adult rat hearts. These cells could differentiate not only into beating myocytes but also into cells of other lineages, including adipocytes and endothelial cells in the methylcellulose‐based medium containing interleukin‐3 (IL‐3), interleukin‐6 (IL‐6), and stem cell factor (SCF). In particular, IL‐3 and SCF contributed to the differentiation into cardiac troponin I‐positive cells. Notably, small population of LA‐PCs coexpressed GATA4 and myogenin, which are markers specific to cardiomyocytes and skeletal myocytes, respectively, and could differentiate into both cardiac and skeletal myocytes. Therefore, we investigated the involvement of these two tissue‐specific transcription factors in the cardiac transcriptional activity. Coexpression of GATA4 and myogenin synergistically activated GATA4‐specific promoter of the atrial natriuretic peptide gene. This combinatorial function was shown to be dependant on the GATA site, but independent of the E‐box. The results of chromatin immunoprecipitation and electrophoretic mobility shift assays suggested that myogenin bound to GATA4 on the GATA elements and the C‐terminal Zn‐finger domain of GATA4 and the N‐terminal region of myogenin were required for this synergistic activation of transcription. Taken together, these two transcription factors could be involved in the myogenesis of LA‐PCs.