白细胞介素-13诱导人气道上皮细胞产生涉及STAT6/SPDEF的粘蛋白5AC。

Q2 Biochemistry, Genetics and Molecular Biology
Cell Communication and Adhesion Pub Date : 2010-08-01 Epub Date: 2011-01-28 DOI:10.3109/15419061.2010.551682
Hongmei Yu, Qi Li, Victor P Kolosov, Juliy M Perelman, Xiangdong Zhou
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引用次数: 79

摘要

粘液分泌过多是许多慢性气道炎性疾病的常见病。Mucin 5AC (MUC5AC)是一种主要的气道粘蛋白,在杯状细胞中高表达。在这里,作者发现了一个被称为SAM结构域的前列腺衍生Ets因子(SPDEF)的基因,它是由白细胞介素(IL)-13诱导的。结果表明,特异性敲低SPDEF可降低il -13诱导的人气道上皮细胞MUC5AC的表达。这一发现与前梯度2 (AGR2)和Ca(2+)激活的Cl(-)通道(CLCA1)的表达降低有关,CLCA1调节il -13介导的MUC5AC过度产生。此外,转染SPDEF siRNA增强了叉头盒a2 (Foxa2)的表达,Foxa2是已知阻止粘液产生的关键转录因子。作者还证实,抑制STAT6可抑制IL-13诱导的SPDEF和MUC5AC的表达。这些结果表明SPDEF在调节il -13诱导的依赖STAT6的MUC5AC合成的转录网络中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interleukin-13 induces mucin 5AC production involving STAT6/SPDEF in human airway epithelial cells.

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.

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来源期刊
Cell Communication and Adhesion
Cell Communication and Adhesion 生物-生化与分子生物学
CiteScore
2.50
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation Cell Communication and Adhesion is an international Open Access journal which provides a central forum for research on mechanisms underlying cellular signalling and adhesion. The journal provides a single source of information concerning all forms of cellular communication, cell junctions, adhesion molecules and families of receptors from diverse biological systems. The journal welcomes submission of original research articles, reviews, short communications and conference reports.
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