...
首页> 外文期刊>Frontiers in bioscience: a journal and virtual library >Recent progress in research on beta-cell apoptosis by cytokines.
【24h】

Recent progress in research on beta-cell apoptosis by cytokines.

机译:细胞因子对β细胞凋亡的研究进展。

获取原文
获取原文并翻译 | 示例
           

摘要

Pancreatic beta-cell apoptosis plays a critical role in the pathogenesis of type 1 diabetes mellitus. As death effector molecules, perforin, Fas ligand, tumor necrosis factor (TNF)-alpha, Interleukin (IL)-1, interferon (IFN)-gamma, and nitric oxide have been claimed. Recently, combinations or synergisms between IFN-gamma and TNF-alpha or IL-1beta are being revisited as the death effectors, and signal transduction of such synergisms has been explored to find molecular mechanism of beta -cell death. Among the regulators of apoptosis, nuclear factor-kappaB (NF-kappaB) has emerged as a master switch of cytokine-induced beta -cell dysfunction and death. By employing TNF-alpha / IFN-gamma synergism model which causes beta -cell apoptosis, we found that the antiapoptotic X-linked inhibitor of apoptosis (XIAP) molecule is upregulated by NF-kappaB in response to TNF-alpha and XIAP induction was inhibited by IFN-gamma-induced signal transducer and activator of transcription-1 (STAT1) activation, which explains the death of beta -cells by TNF-alpha /IFN-gamma synergism.
机译:胰腺β细胞凋亡在1型糖尿病的发病机理中起着至关重要的作用。作为死亡效应分子,穿孔素,Fas配体,肿瘤坏死因子(TNF)-α,白介素(IL)-1,干扰素(IFN)-γ和一氧化氮已被要求保护。近来,IFN-γ和TNF-α或IL-1β之间的组合或协同作用正被重新考虑作为死亡效应物,并且已经探索了这种协同作用的信号转导以发现β-细胞死亡的分子机制。在细胞凋亡的调节剂中,核因子-κB(NF-kappaB)已经成为细胞因子诱导的β细胞功能障碍和死亡的主要开关。通过使用导致β细胞凋亡的TNF-α/IFN-γ协同模型,我们发现NF-κB上调了抗凋亡X连锁凋亡抑制剂(XIAP)分子对TNF-α的响应,并抑制了XIAP的诱导通过IFN-γ诱导的信号转导和转录激活因子1(STAT1)的激活,这解释了TNF-α/IFN-γ协同作用导致β细胞死亡。

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