Key result
Reperfusion-induced myocyte DNA fragmentation occurs exclusively in oncotic, not apoptotic, cells.
Why the study?
Infarcted myocytes have been reported to show apoptosis based on DNA fragmentation at the light microscopic level, leaving it unclear whether TUNEL-positive infarcted myocytes have apoptotic or oncotic ultrastructures.
Does 30-minute coronary artery ischemia followed by varying durations of reperfusion induce apoptotic or oncotic ultrastructures with DNA fragmentation in rabbit myocytes?
Does 30-minute coronary artery ischemia followed by varying durations of reperfusion induce apoptotic or oncotic ultrastructures with DNA fragmentation in rabbit myocytes?
Answers are grounded in this paper and cite their sources.
In a rabbit model of myocardial ischemia-reperfusion, DNA fragmentation and TUNEL positivity occurred exclusively in myocytes with irreversibly oncotic rather than apoptotic ultrastructures, indicating that TUNEL positivity does not necessarily signify apoptosis in infarcted myocardium.
BACKGROUND: Modes of cell death have been defined morphologically as apoptosis and oncosis. Infarcted myocytes have been reported to show apoptosis, as revealed by DNA fragmentation by DNA ladder and by in situ terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) at the light microscopic level. We investigated whether TUNEL-positive infarcted myocytes have apoptotic or oncotic ultrastructures by using electron microscopic TUNEL, which can simultaneously observe the ultrastructure and DNA fragmentation of the same myocytes. METHODS AND RESULTS: Thirty rabbits were divided into 5 groups (n=6 each) that were subjected to a sham operation or to 30-minute ischemia followed by 0-minute, 30-minute, 2-hour, or 4-hour reperfusion of a coronary artery. In the 2- and 4-hour reperfusion groups only, DNA electrophoresis showed a ladder pattern, and the light microscopic TUNEL finding was positive in the nuclei of myocytes localized in the infarcted area (6+/-2% and 11+/-3%, respectively). Electron microscopic TUNEL showed that nuclei with a significant accumulation of immunogold particles (indicating an electronic microscopic TUNEL-positive result) were observed only in the infarcted myocytes with irreversibly oncotic ultrastructures that were found in the hearts of the 2- and 4-hour reperfusion groups (41+/-3% and 83+/-4%, respectively). Irreversibly oncotic myocytes (indicated by swelling, inhomogeneously clumped chromatin in nuclei, dense bodies in mitochondria, and/or ruptured plasma membranes) were also seen in the 0- and 30-minute reperfusion groups, which did not exhibit TUNEL-positive myocytes. There was no evidence of apoptotic ultrastructures in the myocytes. CONCLUSIONS: DNA fragmentation occurs in the myocytes that had already shown irreversibly oncotic, but not apoptotic, ultrastructures with ischemia and/or reperfusion. Therefore, DNA fragmentation itself does not always mean apoptosis, and so-called apoptotic infarcted myocytes may belong to a category of cell death other than apoptosis.
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Ohno et al. (1998) studied Myocardial infarction (ischemia/reperfusion injury) (n=30). Coronary artery ischemia and reperfusion vs. Sham operation was evaluated on Ultrastructure and DNA fragmentation of infarcted myocytes. In a rabbit model of ischemia-reperfusion, DNA fragmentation occurred only in myocytes with irreversibly oncotic, rather than apoptotic, ultrastructures, challenging standard definitions of apoptosis.
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