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Transcriptional profiling defines the molecular signature of embryonic mouse cardiac progenitor cells.
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Transcriptome-wide analysis of dynamically regulated progenitor cell populations has the potential to elucidate key aspects of cardiac development. The heart, as the first organ to develop in the mammal, is a technically challenging but clinically relevant target for study. To define the transcriptional program of the cardiac progenitor, we used a novel transgenic strategy and fluorescence-activated cell sorting to reliably label and isolate cardiac progenitors directly from mouse embryos. Pure populations of cardiac progenitor cells were isolated from the cardiac crescent and 2 subsequent stages of heart development: the linear heart tube and the looping heart. RNA was isolated from stage-specific cardiac progenitors and subjected to transcriptome analysis by oligonucleotide array hybridization. The cardiac transcriptional regulatory programs were compared with the molecular programs of age-matched noncardiac embryonic cells, embryonic stem cells, adult cardiomyocytes, and each other to identify sets of genes exhibiting differential expression in the cardiac progenitor cell population. These results define the transcriptional profile of mammalian cardiac progenitor cells and provide insight into the molecular regulation of the earliest periods of heart development.
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Masino et al. (2004) studied Cardiac development. Transgenic labeling, FACS isolation, and oligonucleotide array transcriptome analysis vs. Age-matched noncardiac embryonic cells, embryonic stem cells, and adult cardiomyocytes was evaluated on Differential gene expression and transcriptional profile of cardiac progenitor cells. Transgenic FACS isolation and array profiling across 3 embryonic stages defined the transcriptional profile of mouse cardiac progenitors compared with noncardiac and adult cardiac cells.
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