Requirement of JNK for Stress- Induced Activation of the Cytochrome c-Mediated Death Pathway
Cathy Tournier(Howard Hughes Medical Institute), Patricia Hess(Howard Hughes Medical Institute), Derek Yang(Howard Hughes Medical Institute), Jie Xu(Howard Hughes Medical Institute), Tod K. Turner(University of Massachusetts Chan Medical School), Anjaruwee S. Nimnual(State University of New York), Dafna Bar‐Sagi(State University of New York), Stephen N. Jones(University of Massachusetts Chan Medical School), Richard A. Flavell(Howard Hughes Medical Institute), Roger J. Davis(Howard Hughes Medical Institute)
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Abstract
The c-Jun NH2-terminal kinase (JNK) is activated when cells are exposed to ultraviolet (UV) radiation. However, the functional consequence of JNK activation in UV-irradiated cells has not been established. It is shown here that JNK is required for UV-induced apoptosis in primary murine embryonic fibroblasts. Fibroblasts with simultaneous targeted disruptions of all the functional Jnk genes were protected against UV-stimulated apoptosis. The absence of JNK caused a defect in the mitochondrial death signaling pathway, including the failure to release cytochrome c. These data indicate that mitochondria are influenced by proapoptotic signal transduction through the JNK pathway.
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