首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Role of glycogen synthase kinase 3 in squamous differentiation induced by cigarette smoke in porcine tracheobronchial epithelial cells.
【24h】

Role of glycogen synthase kinase 3 in squamous differentiation induced by cigarette smoke in porcine tracheobronchial epithelial cells.

机译:糖原合酶激酶3在猪烟气支气管支气管上皮细胞中诱导的鳞状分化中的作用。

获取原文
获取原文并翻译 | 示例
           

摘要

Epidemiological evidence suggests that cigarette smoke induces squamous metaplasia in human tracheobronchial epithelium that can progress to lung squamous carcinoma. But it is not well understood how tracheobronchial epithelial cells transduce the signals that mediate cigarette smoke-induced squamous differentiation or squamous metaplasia. In the present study, we found that in vitro cigarette smoke components notably inhibited glycogen synthase kinase 3 (GSK3) and induced the expression of involucrin, a marker of squamous differentiation. The inactivation of GSK3 by two highly selective inhibitors, lithium and SB216763, also significantly enhanced involucrin expression in cultured porcine tracheobronchial epithelial cells (PTBECs). Moreover, we demonstrated that cigarette smoke components significantly promoted activator protein-1 (AP-1) binding activities to the upstream regulatory region of involucrin gene, and similar results were observed by further studies through using GSK3 inhibitors to imitatethe effects of cigarette smoke components. Taken together, we conclude that GSK3 is involved in involucrin expression induced by cigarette smoke in PTBEC probably via negatively regulating AP-1 activity, implying a possible mechanism responsible for squamous differentiation induced by cigarette smoke.
机译:流行病学证据表明,香烟烟雾可导致人气管支气管上皮鳞状化生,并可能发展为肺鳞癌。但是,人们还不太了解气管支气管上皮细胞如何转导介导香烟烟雾诱导的鳞状分化或鳞状化生的信号。在本研究中,我们发现体外香烟烟雾成分显着抑制糖原合酶激酶3(GSK3)并诱导鳞癌分化标志物involucrin的表达。两种高度选择性的抑制剂锂和SB216763对GSK3的灭活作用也显着增强了培养的猪气管支气管上皮细胞(PTBEC)中的总蛋白表达。此外,我们证明了卷烟烟气成分显着促进了激活蛋白1(AP-1)结合到involucrin基因的上游调节区,并且通过使用GSK3抑制剂模仿卷烟烟气成分的作用,通过进一步研究观察到了相似的结果。两者合计,我们得出结论,GSK3可能通过负调节AP-1活性参与了PTBEC中香烟烟雾诱导的整合素表达,这暗示着可能由香烟烟雾诱导的鳞状分化的机制。

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