Bao Lei, Alexander Jaime B, Zhang Huayi, Shen Kui, Chan Lawrence S
1 Department of Dermatology, University of Illinois at Chicago , Chicago, Illinois.
2 Department of Microbiology & Immunology, University of Illinois at Chicago , Chicago, Illinois.
J Interferon Cytokine Res. 2016 Jun;36(6):374-81. doi: 10.1089/jir.2015.0056. Epub 2016 Feb 26.
Skin barrier defects play an important role in atopic dermatitis (AD). Involucrin, an important barrier protein suppressed in human AD, is downregulated by interleukin-4 (IL-4). However, the molecular mechanism for IL-4 downregulation of involucrin has not been delineated, and especially how Stat6, a transcriptional activator, represses involucrin expression is unknown. Since Stats usually recruit p300/CBP in the general transcription machinery of their target genes and involucrin expression also involves p300/CBP, we hypothesize that Stat6 activated by IL-4 may sequestrate p300/CBP from the involucrin transcription complex, thus suppressing involucrin expression in keratinocytes. Using IL-4 transgenic mice, an AD mouse model, we find that involucrin expression is similarly downregulated as in human AD. In HaCat cells, the Jak inhibitor and dominant negative studies indicate that the Jaks-Stat6 pathway is involved in IL-4 downregulation of involucrin. Next, we transfected HaCat cells with an involucrin promoter-luciferase construct and then treated them with IL-4. IL-4 greatly suppresses the promoter activity, which is totally abolished by cotransfecting the CREB-binding protein (CBP) expression vector, indicating that IL-4 cannot downregulate involucrin in the presence of excess CBP. Finally, chromatin immunoprecipitation assay demonstrates that IL-4 decreases CBP binding to the involucrin transcription complex. For the first time, we defined a molecular mechanism for IL-4 downregulation of involucrin in keratinocytes, which may play an important role in the pathogenesis of AD.
皮肤屏障缺陷在特应性皮炎(AD)中起重要作用。兜甲蛋白是一种在人类AD中被抑制的重要屏障蛋白,它会被白细胞介素4(IL-4)下调。然而,IL-4下调兜甲蛋白的分子机制尚未阐明,尤其是转录激活因子Stat6如何抑制兜甲蛋白表达尚不清楚。由于Stat蛋白通常在其靶基因的一般转录机制中募集p300/CBP,且兜甲蛋白的表达也涉及p300/CBP,我们推测被IL-4激活的Stat6可能会从兜甲蛋白转录复合物中隔离p300/CBP,从而抑制角质形成细胞中兜甲蛋白的表达。使用AD小鼠模型IL-4转基因小鼠,我们发现兜甲蛋白的表达与人类AD中一样被下调。在HaCaT细胞中,Jak抑制剂和显性阴性研究表明Jaks-Stat6途径参与了IL-4对兜甲蛋白的下调。接下来,我们用兜甲蛋白启动子-荧光素酶构建体转染HaCaT细胞,然后用IL-4处理它们。IL-4极大地抑制了启动子活性,通过共转染CREB结合蛋白(CBP)表达载体可完全消除这种抑制,这表明在存在过量CBP的情况下,IL-4不能下调兜甲蛋白。最后,染色质免疫沉淀试验表明IL-4会减少CBP与兜甲蛋白转录复合物的结合。我们首次确定了角质形成细胞中IL-4下调兜甲蛋白的分子机制,这可能在AD的发病机制中起重要作用。