首页> 外文期刊>Cell death and differentiation >p63 regulates the caspase-8-FLIP apoptotic pathway in epidermis.
【24h】

p63 regulates the caspase-8-FLIP apoptotic pathway in epidermis.

机译:p63调节表皮中的caspase-8-FLIP细胞凋亡途径。

获取原文
获取原文并翻译 | 示例
           

摘要

The transcription factor p63, member of the p53 family, is crucial for epithelial development. An RNAi screening identified the apoptotic gene Procaspase-8 as a target activated by p63. The caspase-8 inhibitor FLIP is also under p63 control. We analysed and detailed the direct transactivation through the use of RNAi, reporter assays, ChIPs, western blots, confocal studies in HaCat, as well as in primary human keratinocytes. The direct DeltaNp63 regulation of these targets was confirmed in vivo using transgenic DeltaNp63 mice under the K5 promoter, as compared with p63 knockout mice, and in vitro in normal human primary keratinocytes following UV irradiation. Lowering the steady state of p63 protein levels changes the relative ratio of FLIP isoforms, causing the activation of the expressed, inactive Procaspase-8, into the active isoform thus triggering the proapoptotic cascade. Therefore, p63 fine-tunes the Procaspase-8-FLIP pro- and antiapoptotic pathway in keratinocytes.
机译:转录因子p63是p53家族的成员,对上皮发育至关重要。 RNAi筛选确定凋亡基因Procaspase-8是p63激活的靶标。 caspase-8抑制剂FLIP也处于p63控制之下。我们通过在HaCat以及人类原代角质形成细胞中使用RNAi,报告基因分析,ChIP,Western印迹,共聚焦研究来分析和详述直接反式激活。与p63基因敲除小鼠相比,在K5启动子下使用转基因DeltaNp63小鼠在体内证实了这些靶标的直接DeltaNp63调节,在紫外线照射后在正常人原代角质形成细胞中在体外证实了这些靶标的直接DeltaNp63调节。降低p63蛋白水平的稳定状态会改变FLIP同工型的相对比例,从而导致表达的非活性Procaspase-8活化为活性同工型,从而触发促凋亡级联反应。因此,p63可微调角质形成细胞中的Procaspase-8-FLIP促凋亡途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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