TY - JOUR
T1 - Akt protein kinase inhibits non-apoptotic programmed cell death induced by ceramide
AU - Mochizuki, Toshihiro
AU - Asai, Akio
AU - Saito, Nobuhito
AU - Tanaka, Sakae
AU - Katagiri, Hideki
AU - Asano, Tomoichiro
AU - Nakane, Makoto
AU - Tamura, Akira
AU - Kuchino, Yoshiyuki
AU - Kitanaka, Chifumi
AU - Kirino, Takaaki
PY - 2002/1/25
Y1 - 2002/1/25
N2 - A growing body of evidence now suggests that programmed cell death (PCD) occurs via non-apoptotic mechanisms as well as by apoptosis. In contrast to apoptosis, however, the molecular mechanisms involved in the regulation of non-apoptotic PCD remain only poorly understood. Here we show that ceramide induces a nonapoptotic PCD with a necrotic-like morphology in human glioma cells. Characteristically, the cell death was not accompanied by loss of the mitochondrial transmembrane potential, cytosolic release of cytochrome c from mitochondria, or the activation of the caspase cascade. Consistent with these characteristics, this ceramide-induced cell death was inhibited neither by the overexpression of Bcl-xL nor by the pan-caspase inhibitor zVAD-fmk. However, strikingly, the ceramide-induced non-apoptotic cell death was inhibited by the activation of the Akt/protein kinase B pathway through the expression of a constitutively active version of Akt. The results for the first time indicate that the Akt kinase, known to play an essential role in survival factor-mediated inhibition of apoptotic cell death, is also involved in the regulation of non-apoptotic PCD.
AB - A growing body of evidence now suggests that programmed cell death (PCD) occurs via non-apoptotic mechanisms as well as by apoptosis. In contrast to apoptosis, however, the molecular mechanisms involved in the regulation of non-apoptotic PCD remain only poorly understood. Here we show that ceramide induces a nonapoptotic PCD with a necrotic-like morphology in human glioma cells. Characteristically, the cell death was not accompanied by loss of the mitochondrial transmembrane potential, cytosolic release of cytochrome c from mitochondria, or the activation of the caspase cascade. Consistent with these characteristics, this ceramide-induced cell death was inhibited neither by the overexpression of Bcl-xL nor by the pan-caspase inhibitor zVAD-fmk. However, strikingly, the ceramide-induced non-apoptotic cell death was inhibited by the activation of the Akt/protein kinase B pathway through the expression of a constitutively active version of Akt. The results for the first time indicate that the Akt kinase, known to play an essential role in survival factor-mediated inhibition of apoptotic cell death, is also involved in the regulation of non-apoptotic PCD.
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U2 - 10.1074/jbc.M106361200
DO - 10.1074/jbc.M106361200
M3 - Article
C2 - 11706021
AN - SCOPUS:18544364918
SN - 0021-9258
VL - 277
SP - 2790
EP - 2797
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 4
ER -