首页> 外文OA文献 >Phosphatidylinositol 3-kinase mediates epidermal growth factor-induced activation of the c-Jun N-terminal kinase signaling pathway.
【2h】

Phosphatidylinositol 3-kinase mediates epidermal growth factor-induced activation of the c-Jun N-terminal kinase signaling pathway.

机译:磷脂酰肌醇3-激酶介导表皮生长因子诱导的c-Jun N-末端激酶信号通路的激活。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The signaling events which mediate activation of c-Jun N-terminal kinase (JNK) are not yet well characterized. To broaden our understanding of upstream mediators which link extracellular signals to the JNK pathway, we investigated the role of phosphatidylinositol (PI) 3-kinase in epidermal growth factor (EGF)-mediated JNK activation. In this report we demonstrate that a dominant negative form of PI 3-kinase as well as the inhibitor wortmannin blocks EGF-induced JNK activation dramatically. However, wortmannin does not have an effect on JNK activation induced by UV irradiation or osmotic shock. In addition, a membrane-targeted, constitutively active PI 3-kinase (p110beta) was shown to produce in vivo products and to activate JNK, while a kinase-mutated form of this protein showed no activation. On the basis of these experiments, we propose that PI 3-kinase activity plays a role in EGF-induced JNK activation in these cells.
机译:介导c-Jun N端激酶(JNK)激活的信号转导事件尚未得到很好的表征。为了拓宽对将细胞外信号连接至JNK途径的上游介质的了解,我们研究了磷脂酰肌醇(PI)3-激酶在表皮生长因子(EGF)介导的JNK激活中的作用。在本报告中,我们证明了PI 3激酶的显性负向形式以及抑制剂渥曼青霉素可以显着阻断EGF诱导的JNK活化。但是,渥曼青霉素对紫外线辐射或渗透压引起的JNK活化没有影响。此外,膜靶向的,组成型活性的PI 3-激酶(p110beta)被证明可以产生体内产物并激活JNK,而这种蛋白的激酶突变形式则没有激活。在这些实验的基础上,我们建议PI 3-激酶活性在这些细胞中EGF诱导的JNK激活中起作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号