Advertisement
Research Article Free access | 10.1172/JCI119114
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Krown, K. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Page, M. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Nguyen, C. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Zechner, D. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Gutierrez, V. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Comstock, K. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Glembotski, C. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Quintana, P. in: JCI | PubMed | Google Scholar
Department of Biology, San Diego State University, California 92182, USA.
Find articles by Sabbadini, R. in: JCI | PubMed | Google Scholar
Published December 15, 1996 - More info
In the present study, it was shown that physiologically relevant levels of the proinflammatory cytokine TNFalpha induced apoptosis in rat cardiomyocytes in vitro, as quantified by single cell microgel electrophoresis of nuclei ("cardiac comets") as well as by morphological and biochemical criteria. It was also shown that TNFalpha stimulated production of the endogenous second messenger, sphingosine, suggesting sphingolipid involvement in TNFalpha-mediated cardiomyocyte apoptosis. Consistent with this hypothesis, sphingosine strongly induced cardiomyocyte apoptosis. The ability of the appropriate stimulus to drive cardiomyocytes into apoptosis indicated that these cells were primed for apoptosis and were susceptible to clinically relevant apoptotic triggers, such as TNFalpha. These findings suggest that the elevated TNFalpha levels seen in a variety of clinical conditions, including sepsis and ischemic myocardial disorders, may contribute to TNFalpha-induced cardiac cell death. Cardiomyocyte apoptosis is also discussed in terms of its potential beneficial role in limiting the area of cardiac cell involvement as a consequence of myocardial infarction, viral infection, and primary cardiac tumors.