Apoptosis mediates the disappearance of infiltrated leukocytes and proliferated interstitial cells after MI, with apoptotic cells peaking at 2 days (5.3-6.9%) and decreasing by 4 weeks (0.5%).
Apoptosis plays an important role in the disappearance of infiltrated leukocytes and proliferated interstitial cells during the healing stage after myocardial infarction, which may have implications for postinfarct ventricular remodeling.
Myocardial infarction (MI) progresses from the acute death of myocytes and the infiltration of inflammatory cells into granulation, followed by scars. During the healing process, the myocardial interstitial cell population in the infarcted tissues increases markedly and then decreases. We postulated that apoptosis is responsible for this process. Twenty-four male Japanese white rabbits underwent a 30-minute occlusion of the left coronary artery followed by reperfusion for 2 days, 2 weeks, or 4 weeks (n=8 each). The histological features consisted of dead cardiomyocytes and marked leukocyte infiltration at 2 days after MI and granulation consisting of numerous alpha-smooth muscle actin-positive myofibroblasts, macrophage antigen-positive macrophages, and neovascularization at 2 weeks. At 4 weeks, the cellularity decreased markedly, and scars were evident. Interstitial cells with positive nick end labeling were significantly more frequent at the light microscopic level in the 2-day MI samples (5.3+/-3.6% in the center and 6.9+/-3.3% in the periphery of the infarct region) than in the 2-week (2.5+/-1.0%) and 4-week (0.5+/-0.5%) samples. DNA electrophoresis showed a clear ladder in tissues from the ischemic areas at 2 days after MI but not at 2 and 4 weeks after MI. Ultrastructurally, typical apoptotic figures, including apoptotic bodies and condensed nuclei without ruptured plasma membranes, were detected in leukocytes from all hearts with 2-day MI and in myofibroblasts, endothelial cells, and macrophages from all hearts with 2-week MI. In the electron microscopic in situ nick end labeling, immunogold particles intensely labeled the condensed chromatin of the typical apoptotic nuclei. These particles were also accumulated on nuclei of the interstitial cells showing homogeneous density but not definite condensation as typical apoptotic nuclei, suggesting an early stage of apoptosis. Thus, apoptosis plays an important role in the disappearance of both the infiltrated leukocytes and the proliferated interstitial cells after MI. This finding may have therapeutic implications for postinfarct ventricular remodeling through apoptosis handling during the healing stage of MI.
Takemura et al. (1998) studied Myocardial infarction (n=24). 30-minute occlusion of the left coronary artery followed by reperfusion vs. Different reperfusion durations (2 days, 2 weeks, 4 weeks) was evaluated on Frequency of interstitial cells with positive nick end labeling. Apoptosis mediates the disappearance of infiltrated leukocytes and proliferated interstitial cells after MI, with apoptotic cells peaking at 2 days (5.3-6.9%) and decreasing by 4 weeks (0.5%).