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. Author manuscript; available in PMC: 2011 May 11.
Published in final edited form as: Circulation. 2010 Apr 26;121(18):1992–2000. doi: 10.1161/CIRCULATIONAHA.109.909093

Figure 3. Cardiac-resident c-kit+ cells from neonatal hearts exhibit robust cardiomyogenic differentiation when co-cultured with fetal cardiomyocytes.

Figure 3

Non-transgenic fetal cardiomyocyte cultures were seeded with neonatal c-kit+ cells from ACT-EGFP/MHC-nLAC double transgenic hearts and cultured for 7 days. The cultures were then fixed and processed for β-galactosidase activity (blue), EGFP (green) and α-actinin (red) immune reactivity. EGFP-expressing cardiomyocytes exhibiting mature sarcomeric structure (yellow due to the overlay of green EGFP and red α-actinin signals) were readily detected by fluorescence microscopy; these cells also exhibited β-galactosidase activity when visualized under bright field illumination (inset). Bar = 20 microns in the fluorescent image, 20 microns in the bright field inset. Arrows mark β-galactosidase+ nuclei. Bright field, single color fluorescence and merged images for these cells are shown in the Supplemental Data section.