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. Author manuscript; available in PMC: 2009 Jul 2.
Published in final edited form as: Circ Res. 2008 Nov 26;104(1):e1–e7. doi: 10.1161/CIRCRESAHA.108.188649

Figure 4.

Figure 4

Assessment of cardiomyocyte proliferation 7 days after MI in Pn−/− and PntTA transgenic mice. A, Western blot analysis of periostin in the heart following MI. GAPDH is a loading control. B, Percent of BrdU positive cardiomyocyte nuclei when compared to total cardiomyocyte nuclei in the peri-infarct area of Pn−/−, PntTA mice and their appropriate controls. Below the graph a representative immunohistological image is shown with labeled non-myocytes (asterisk) and a labeled myocyte (arrow). C, Percent of phosphorylated histone H3 positive cardiomyocytes compared to total cardiomyocytes in the peri-infarct area of Pn−/−, PntTA mice and their appropriate controls. Below the graph a representative immunohistological image is shown with a labeled non-myocyte (asterisk) and a labeled myocyte (arrow). Experiments were performed on a minimum of 4 hearts per cohort. Greater then 100,000 cells were counted per experimental group. None of the groups were significantly different.