Molecular biology of the cell, 2004-02, Vol.15 (2), p.922-933
2004
Volltextzugriff (PDF)
Details
- Autor(en) / Beteiligte
- Titel
- P38 alpha mitogen-activated protein kinase sensitizes cells to apoptosis induced by different stimuli
- Ist Teil von
- Molecular biology of the cell, 2004-02, Vol.15 (2), p.922-933
- Ort / Verlag
- United States: The American Society for Cell Biology
- Erscheinungsjahr
- 2004
- Quelle
- MEDLINE
- Beschreibungen/Notizen
- p38 alpha mitogen-activated protein (MAP) kinase is a broadly expressed signaling molecule that participates in the regulation of cellular responses to stress as well as in the control of proliferation and survival of many cell types. We have used cell lines derived from p38 alpha knockout mice to study the role of this signaling pathway in the regulation of apoptosis. Here, we show that cardiomyocytes and fibroblasts lacking p38 alpha are more resistant to apoptosis induced by different stimuli. The reduced apoptosis of p38 alpha-deficient cells correlates with decreased expression of the mitochondrial proapoptotic protein Bax and the apoptosis-inducing receptor Fas/CD-95. Cells lacking p38 alpha also have increased extracellular signal-regulated kinase (ERKs) MAP kinase activity, and the up-regulation of this survival pathway seems to be at least partially responsible for the reduced levels of apoptosis in the absence of p38 alpha. Phosphorylation of the transcription factor STAT3 on Ser-727, mediated by the extracellular signal-regulated kinase MAP kinase pathway, may contribute to the decrease in both Bax and Fas expression in p38 alpha-/- cells. Thus, p38 alpha seems to sensitize cells to apoptosis via both up-regulation of proapoptotic proteins and down-regulation of survival pathways.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 1059-1524eISSN: 1939-4586DOI: 10.1091/mbc.E03-08-0592Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_329404
- Format
- –
- Schlagworte
- Animals, Apoptosis - drug effects, Apoptosis - physiology, bcl-2-Associated X Protein, Cells, Cultured, DNA-Binding Proteins - metabolism, Embryo, Mammalian - metabolism, Enzyme Activation - physiology, fas Receptor - pharmacology, Fibroblasts - metabolism, MAP Kinase Signaling System - drug effects, MAP Kinase Signaling System - physiology, Mice, Mice, Knockout, Mitogen-Activated Protein Kinase 14, Mitogen-Activated Protein Kinases - metabolism, Myocytes, Cardiac - metabolism, Phosphorylation - drug effects, Proto-Oncogene Proteins - metabolism, Proto-Oncogene Proteins c-bcl-2, Signal Transduction - drug effects, STAT3 Transcription Factor, Trans-Activators - metabolism