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Interleukin-13 Induces Mucin 5AC Production Involving STAT6/SPDEF in Human Airway Epithelial Cells

机译:白细胞介素13诱导人类呼吸道上皮细胞中涉及STAT6 / SPDEF的粘蛋白5AC生产。

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摘要

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.
机译:在许多慢性气道炎性疾病中通常观察到粘液分泌过多。粘蛋白5AC(MUC5AC)是主要的气道粘蛋白,因为它在杯状细胞中高表达。在这里,作者鉴定了一个称为SAM结构域的基因,该基因包含由白介素(IL)-13诱导的前列腺衍生的Ets因子(SPDEF)。他们的结果表明,SPDEF的特异性抑制可降低IL-13诱导的人气道上皮细胞中MUC5AC的表达。这一发现与前梯度2(AGR2)和Ca〜(2 ++)激活的Cl〜(δ)通道(CLCA1)的表达降低有关,后者调节IL-13介导的MUC5AC的过度生产。此外,用SPDEF siRNA转染可增强叉头盒a2(Foxa2)的表达,叉头盒a2是已知可防止粘液产生的关键转录因子。作者还证明抑制STAT6可抑制IL-13诱导的SPDEF和MUC5AC的表达。这些结果表明,SPDEF在调节依赖STAT6的介导IL-13诱导的MUC5AC合成的转录网络中起关键作用。

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