| Literature DB >> 10797012 |
C Tournier1, P Hess, D D Yang, J Xu, T K Turner, A Nimnual, D Bar-Sagi, S N Jones, R A Flavell, R J Davis.
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.Entities:
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Year: 2000 PMID: 10797012 DOI: 10.1126/science.288.5467.870
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728