...
首页> 外文期刊>Biochemical and Biophysical Research Communications >Effect of thymic stromal lymphopoietin on MUC5B expression in human airway epithelial cells
【24h】

Effect of thymic stromal lymphopoietin on MUC5B expression in human airway epithelial cells

机译:胸腺基质淋巴细胞生成素对人气道上皮细胞中MUC5B表达的影响

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Thymic stromal lymphopoietin (TSLP) is an interleukin 7-like cytokine and a potent factor for B- and T-cell growth and differentiation. Recent studies have demonstrated an association of TSLP with allergic and inflammatory airway diseases. However, no study on the effect of TSLP on expression of mucin genes in airway epithelial cells has been reported. Therefore, the effects and brief signaling pathways of TSLP on expression of mucin genes in human airway epithelial cells were investigated in this study. In mucin-producing human NCI-H292 airway epithelial cells and primary cultures of normal nasal epithelial cells, the effect and signaling pathway of TSLP on expression of mucin genes were investigated using reverse transcriptase-polymerase chain reaction (RT-PCR), real-time PCR, enzyme immunoassay, and immunoblot analysis with several specific inhibitors and small interfering RNA (siRNA). In human NCI-H292 airway epithelial cells, TSLP increased MUC5B expression. TSLP significantly activated phosphorylation of ERK1/2 and p38 mitogen-activated protein kinase (MAPK). U0126 (ERK1/2 MAPK inhibitor) and SB203580 (p38 MAPK inhibitor) significantly attenuated TSLP-induced MUC5B mRNA expression. Knockdown of ERK1, ERK2, and p38 MAPK by ERK1, ERK2, and p38 MAPK siRNA significantly blocked TSLP-induced MUC5B mRNA expression. In the primary cultures of normal nasal epithelial cells, TSLP significantly increased MUC5B mRNA expression, which was significantly attenuated after pretreatment with U0126 and SB203580. These results suggest that TSLP induces MUC5B expression via the ERK1/2 and p38 MAPK signaling pathway in human airway epithelial cells.
机译:胸腺基质淋巴细胞生成素(TSLP)是一种白介素7样细胞因子,是B细胞和T细胞生长和分化的有效因子。最近的研究表明TSLP与过敏性和炎症性气道疾病相关。然而,尚未有关于TSLP对气道上皮细胞中粘蛋白基因表达影响的研究。因此,本研究探讨了TSLP对人气道上皮细胞黏蛋白基因表达的影响和短暂的信号通路。在产生粘蛋白的人NCI-H292气道上皮细胞和正常鼻上皮细胞的原代培养物中,使用逆转录聚合酶链反应(RT-PCR)实时研究了TSLP对粘蛋白基因表达的影响和信号通路使用几种特异性抑制剂和小干扰RNA(siRNA)进行PCR,酶免疫测定和免疫印迹分析。在人NCI-H292气道上皮细胞中,TSLP增加了MUC5B的表达。 TSLP显着激活ERK1 / 2和p38丝裂原活化蛋白激酶(MAPK)的磷酸化。 U0126(ERK1 / 2 MAPK抑制剂)和SB203580(p38 MAPK抑制剂)显着减弱了TSLP诱导的MUC5B mRNA表达。 ERK1,ERK2和p38 MAPK siRNA敲低ERK1,ERK2和p38 MAPK可以显着阻断TSLP诱导的MUC5B mRNA表达。在正常鼻上皮细胞的原代培养中,TSLP显着增加了MUC5B mRNA的表达,在用U0126和SB203580预处理后,其表达明显减弱。这些结果表明,TSLP通过人气道上皮细胞中的ERK1 / 2和p38 MAPK信号传导途径诱导MUC5B表达。

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