Apoptosis signal-regulating kinase 1 is involved not only in apoptosis but also in non-apoptotic cardiomyocyte death |
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Authors: | Watanabe Tetsuya Otsu Kinya Takeda Toshihiro Yamaguchi Osamu Hikoso Shungo Kashiwase Kazunori Higuchi Yoshiharu Taniike Masayuki Nakai Atsuko Matsumura Yasushi Nishida Kazuhiko Ichijo Hidenori Hori Masatsugu |
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Affiliation: | Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan. |
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Abstract: | ![]() The molecular basis of myocardial cell death in the ischemia-reperfused heart still remains to be clarified. Apoptosis signal-regulating kinase 1 (ASK1) is a mitogen-activated protein kinase kinase kinase that plays an important role in stress-induced apoptosis. We studied ASK1(-/-) mice to examine the role of ASK1 in ischemia-reperfusion injury. In the wild-type heart, ischemia-reperfusion resulted in necrotic injury, whereas infarct size was drastically reduced in the ASK1(-/-) heart. The necrotic injury was not accompanied with any evidence of apoptosis such as an increase in TUNEL-positive cells, DNA fragmentation or the activation of caspase-3. ASK1(-/-) cardiomyocytes were more resistant to H(2)O(2)- or Ca(2+)-induced apoptotic and non-apoptotic cell death compared with wild-type cells. These data suggest that ASK1 is involved in necrosis as well as apoptosis and that ASK1-dependent necrosis is likely to contribute to myocardial cell death in the ischemia-reperfused heart. |
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Keywords: | ASK1 Ischemia-reperfusion injury Non-apoptotic cell death |
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