Expression of epithelial and mesenchymal markers in <i>Sca-1<sup>+</sup>/CD34<sup>+,</sup><sup>−</sup></i> cells.

Abstract

<p><b>Panel A:</b> The expression of epithelial and mesenchymal transcripts was tested by analytical PCR and is illustrated in a hierarchical cluster heatmap. The analysis shows that the majority of <i>Sca-1<sup>+</sup>/CD34<sup>+</sup></i> cells (light grey) show similar marker expression as <i>Sca-1<sup>−/</sup>CD34<sup>+</sup></i> cells (white), while all <i>Sca-1<sup>+</sup>/CD34</i><sup>−</sup> cells (dark grey) are located in the second branch. Red squares indicate specific bands in analytical PCR, black squares indicate negative PCR results. <b>Panel B:</b> FACS analysis reveals EpCAM<sup>+</sup>/Pdgfrα<sup>+</sup> subpopulation within Sca-1<sup>+</sup>/CD34<sup>−/</sup>CD31<sup>−/</sup>CD45<sup>−</sup> cells. For each of 5 mice, 5×10<sup>6</sup> murine lung cells were isolated from lung explants and stained with antibodies directed against Sca-1, CD34, CD31, CD45, Pdgfrα and Epcam. While Sca-1<sup>+</sup>/CD34<sup>−</sup> cells consistently showed Epcam expression, Pdgfrα expression was predominantly found in Sca-1<sup>+</sup>/CD34<sup>+</sup> cells. However, Sca-1<sup>+</sup>/CD34<sup>−/</sup>Epcam<sup>+</sup> cells could be divided in two major subpopulations defined by Pdgfrα expression. Relative quantification is given for corresponding selected subpopulation as indicated by arrows. <b>Panel C:</b> Scatter plots of the detected cell populations for mouse 5, only.</p

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