Tournier C, Hess P, Yang D D, Xu J, Turner T K, Nimnual A, Bar-Sagi D, Jones S N, Flavell R A, Davis R J
Howard Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry & Molecular Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Science. 2000 May 5;288(5467):870-4. doi: 10.1126/science.288.5467.870.
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.
当细胞暴露于紫外线(UV)辐射时,c-Jun氨基末端激酶(JNK)会被激活。然而,JNK激活在紫外线照射细胞中的功能后果尚未明确。本文表明,JNK是原代小鼠胚胎成纤维细胞中紫外线诱导凋亡所必需的。同时靶向破坏所有功能性Jnk基因的成纤维细胞可免受紫外线刺激的凋亡影响。JNK的缺失导致线粒体死亡信号通路出现缺陷,包括细胞色素c未能释放。这些数据表明线粒体受到通过JNK途径的促凋亡信号转导的影响。