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. 2021 Apr 21;11:8669. doi: 10.1038/s41598-021-88159-x

Figure 2.

Figure 2

mRNA expression profile of Tnnt2high and Tnnt2low cardiomyocytes from Wild type and Glut1 transgenic hearts at P1. (a) Representative dot plot of flow cytometry analysis of P1 Wild type hearts for Tnnt2 (cardiac marker) and Mitotracker (mitochondrial contents). Note two populations of cardiomyocytes. (b) Flow cytometry analysis of P1 aMHC-Cre tg; R26+/YFP reporter and aMHC-hGLUT1 tg; aMHC-Cre tg; R26+/YFP reporter analysis for YFP (cardiac lineage) and Mitotracker (mitochondrial contents). Note two populations of cardiomyocytes. (c) Venn diagram of mRNA expressed in Tnnt2high and Tnnt2low cardiomyocytes from Wild type and Glut1 transgenic hearts. Bar graphs represent top three gene ontology (GO) term enriched in the genes uniquely expressed in each population. Although 4 populations are similar, G1 Tnnt2low cardiomyocytes are enriched for the genes associated with mitosis, cell cycle, and cell division. (d) GO analysis of the genes upregulated in Glut1 tg Tnnt2low vs Glut1 tg Tnnt2high. (e) Heatmap of expression level of representative cardiac, cell cycle, and mitochondrial genes differentially expressed in Glut1 tg Tnnt2low vs Glut1 tg Tnnt2high.