AbstractThe mechanisms of cell death induced by hypoxia or ischemia are not yet fully understood. We have previously demonstrated that cell death induced by hypoxia occurs independently of caspases, and is mediated by phospholipase A2 (PLA2).Here, we show that p38 mitogen-activated protein kinase is activated under hypoxia. A selective inhibitor of p38 or decrease in the p38alpha protein level prevents hypoxia-induced cell death. The p38 inhibitor abolishes PLA2 activation by hypoxia, indicating that p38 acts upstream of PLA2. The antioxidant N-acetyl-cysteine inhibits activation of p38 and cell death induced by hypoxia, indicating that reactive oxygen species (ROS) are responsible for p38 activation. These results demonstrate that the ROS/...
Among the three morphologically distinct forms of cell death (apoptosis; autophagic cell death; necr...
The pro-inflammatory activity of Tumor necrosis factor-alpha (TNF-α) together with tissue hypoxia de...
L826–L833, 2004. First published December 12, 2003; 10.1152/ ajplung.00119.2003.—Lung epithelial cel...
AbstractThe mechanisms of cell death induced by hypoxia or ischemia are not yet fully understood. We...
Background: p38 MAPK participates in gases-induced apoptosis signal transmission though it hasn’t mo...
PURPOSE AND EXPERIMENTAL DESIGN: Previously, we observed that the activation of p38 mitogen-activate...
AbstractWe have attempted to elucidate the mechanism of apoptotic cell death induced by hypoxia (ver...
Background: Many diseases and pathological conditions are characterized by transient or constitutive...
Adequate responses to environmental stresses are essential for cell survival. The regulation of cell...
Summaryp38α is a stress-activated protein kinase that negatively regulates malignant transformation ...
International audienceMalignant tumors contain a significant fraction of microregions that are chron...
Activation of p38 mitogen-activated protein kinase (MAPK) plays a central role in cellular responses...
AbstractShort-term (1 h) exposure of cells to a low steady-state concentration of H2O2 causes no imm...
International audienceOxidative stress is a leading cause of endothelial dysfunction. The p38 MAPK p...
Activation of p38 mitogen-activated protein kinase (MAPK) plays a central role in cellular responses...
Among the three morphologically distinct forms of cell death (apoptosis; autophagic cell death; necr...
The pro-inflammatory activity of Tumor necrosis factor-alpha (TNF-α) together with tissue hypoxia de...
L826–L833, 2004. First published December 12, 2003; 10.1152/ ajplung.00119.2003.—Lung epithelial cel...
AbstractThe mechanisms of cell death induced by hypoxia or ischemia are not yet fully understood. We...
Background: p38 MAPK participates in gases-induced apoptosis signal transmission though it hasn’t mo...
PURPOSE AND EXPERIMENTAL DESIGN: Previously, we observed that the activation of p38 mitogen-activate...
AbstractWe have attempted to elucidate the mechanism of apoptotic cell death induced by hypoxia (ver...
Background: Many diseases and pathological conditions are characterized by transient or constitutive...
Adequate responses to environmental stresses are essential for cell survival. The regulation of cell...
Summaryp38α is a stress-activated protein kinase that negatively regulates malignant transformation ...
International audienceMalignant tumors contain a significant fraction of microregions that are chron...
Activation of p38 mitogen-activated protein kinase (MAPK) plays a central role in cellular responses...
AbstractShort-term (1 h) exposure of cells to a low steady-state concentration of H2O2 causes no imm...
International audienceOxidative stress is a leading cause of endothelial dysfunction. The p38 MAPK p...
Activation of p38 mitogen-activated protein kinase (MAPK) plays a central role in cellular responses...
Among the three morphologically distinct forms of cell death (apoptosis; autophagic cell death; necr...
The pro-inflammatory activity of Tumor necrosis factor-alpha (TNF-α) together with tissue hypoxia de...
L826–L833, 2004. First published December 12, 2003; 10.1152/ ajplung.00119.2003.—Lung epithelial cel...