Suppr超能文献

白细胞介素-13通过STAT6/SPDEF诱导人呼吸道上皮细胞产生黏蛋白5AC。

Interleukin-13 induces mucin 5AC production involving STAT6/SPDEF in human airway epithelial cells.

作者信息

Yu Hongmei, Li Qi, Kolosov Victor P, Perelman Juliy M, Zhou Xiangdong

机构信息

Division of Respiratory Medicine, Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.

出版信息

Cell Commun Adhes. 2010 Aug;17(4-6):83-92. doi: 10.3109/15419061.2010.551682. Epub 2011 Jan 28.

Abstract

Mucus hypersecretion is commonly observed in many chronic airway inflammatory diseases. Mucin 5AC (MUC5AC) is a major airway mucin because of its high expression in goblet cells. Here, the authors identified a gene called SAM domain-containing prostate-derived Ets factor (SPDEF) that was induced by interleukin (IL)-13. Their results showed that specific knockdown of SPDEF reduced IL-13-induced MUC5AC expression in human airway epithelial cells. This finding was associated with decreased expression of anterior gradient 2 (AGR2) and Ca(2+)-activated Cl(-) channel (CLCA1), which regulate IL-13-mediated MUC5AC overproduction. Furthermore, transfection with SPDEF siRNA enhanced expression of forkhead box a2 (Foxa2), a key transcription factor that is known to prevent mucus production. The authors also demonstrated that the repression of STAT6 inhibited expression of SPDEF and MUC5AC induced by IL-13. These results show that SPDEF plays a critical role in regulating a transcriptional network mediating IL-13-induced MUC5AC synthesis dependent on STAT6.

摘要

黏液高分泌在许多慢性气道炎症性疾病中普遍存在。黏蛋白5AC(MUC5AC)是一种主要的气道黏蛋白,因为它在杯状细胞中高表达。在此,作者鉴定出一种名为含SAM结构域的前列腺源性Ets因子(SPDEF)的基因,该基因由白细胞介素(IL)-13诱导。他们的结果表明,特异性敲低SPDEF可降低人气道上皮细胞中IL-13诱导的MUC5AC表达。这一发现与前梯度2(AGR2)和钙激活氯离子通道(CLCA1)的表达降低有关,这两种因子调节IL-13介导的MUC5AC过量产生。此外,用SPDEF siRNA转染可增强叉头框a2(Foxa2)的表达,Foxa2是一种已知可阻止黏液产生的关键转录因子。作者还证明,STAT6的抑制可抑制IL-13诱导的SPDEF和MUC5AC的表达。这些结果表明,SPDEF在调节依赖于STAT6的介导IL-13诱导的MUC5AC合成的转录网络中起关键作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验