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应激活化细胞色素c介导的死亡途径对JNK的需求。

Requirement of JNK for stress-induced activation of the cytochrome c-mediated death pathway.

作者信息

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

机构信息

Howard Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry & Molecular Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Science. 2000 May 5;288(5467):870-4. doi: 10.1126/science.288.5467.870.

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.

摘要

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。

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