Key result
Temporally and spatially restricted apoptosis in the outflow tract myocardium, peaking at stages 27-32, supports the docking of the aorta and pulmonary artery with the proper ventricle.
Temporally and spatially restricted apoptosis in the outflow tract myocardium appears critical for the proper docking of the aorta and pulmonary artery during embryonic heart development.
Provides no basis to alter congenital heart defect care; extends apoptosis mapping in avian OFT models.
The outflow tract (OFT) is abnormal in many congenital heart defects. One critical mechanism for morphogenesis of this complex structure is apoptosis. Chicken embryos (stages 19-38; ED4-10) stained with a fluorescent supravital lysosomal dye (LysoTracker Red; LTR) revealed the three-dimensional relationship between structural changes and apoptosis. The LTR staining peaked in the OFT myocardium at stages 27-32, consistent with our previous analyses using other apoptosis assays. While LTR stained under both the pulmonary artery and the aorta, it was most prevalent in the subaortic myocardium before its elimination. Furthermore, LTR staining was most abundant in the myocardium under intensely cytokeratin-positive, thick epicardium. These data support the hypothesis that temporally and spatially restricted apoptosis in the OFT myocardium allows the aorta and pulmonary artery to dock at the appropriate angle and level with the proper ventricle. These data also support a relationship between the differentiating epicardium and cardiomyocyte apoptosis.
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Schaefer et al. (2004) studied Developing heart / Congenital heart defects. Fluorescent supravital lysosomal dye (LysoTracker Red; LTR) staining was evaluated on Apoptosis patterns in the outflow tract myocardium. Temporally and spatially restricted apoptosis in the outflow tract myocardium, peaking at stages 27-32, supports the docking of the aorta and pulmonary artery with the proper ventricle.
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