Yu Hongmei, Li Qi, Kolosov Victor P, Perelman Juliy M, Zhou Xiangdong
Division of Respiratory Medicine, Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Cell Commun Adhes. 2010 Aug;17(4-6):83-92. doi: 10.3109/15419061.2010.551682. Epub 2011 Jan 28.
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.
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。