首页> 美国卫生研究院文献>Biochemical Journal >Interferon-gamma-dependent stimulation of human involucrin gene expression: STAT1 (signal transduction and activators of transcription 1) protein activates involucrin promoter activity.
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Interferon-gamma-dependent stimulation of human involucrin gene expression: STAT1 (signal transduction and activators of transcription 1) protein activates involucrin promoter activity.

机译:干扰素对人inluclucrin基因表达的γ依赖性刺激:STAT1(信号转导和转录激活因子1)蛋白激活involucrin启动子活性。

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摘要

Involucrin is one of the precursor proteins of the cornified cell envelope of keratinocytes, and is expressed during the later stages of keratinocyte differentiation. Interferon-gamma (IFN-gamma), a pleiotropic cytokine with anti-proliferative and immunomodulatory activities, is also a potent inducer of squamous differentiation. Using cultured normal human keratinocytes (NHK cells) and simian virus 40-transformed human keratinocytes (SVHK cells), we investigated the effects of IFN-gamma on involucrin gene expression. Expression of involucrin was increased by about 3-fold after treating NHK cells with IFN-gamma (100 units/ml). Northern blot analyses revealed that IFN-gamma increased the expression of involucrin mRNA. The fragment +42 to -2463 in the 5'-flanking region of the human involucrin gene was subcloned into a luciferase reporter vector and the construct (p2463Luc) was transfected into SVHK cells. p2463Luc produced a 3-fold increase in luciferase activity after IFN-gamma treatment. Sequence analysis detected two putative IFN-gamma-responsive regions [G1 (positions -883 to -874) and G2 (-784 to -775)]. Deletion analyses of the p2463Luc vector revealed that the G1 region is critical for the IFN-gamma-dependent up-regulation of the involucrin gene. Gel-shift analyses revealed that STAT1 (signal transduction and activators of transcription 1) protein bound to the G1 region and that involucrin promoter activity was augmented by transfection of a STAT1 expression vector in the presence of IFN-gamma. In contrast, transfection of a STAT1 dominant-negative expression vector suppressed the IFN-gamma-dependent up-regulation of involucrin promoter activity. These results indicate that IFN-gamma stimulates expression of the human involucrin gene via the G1 (-883 to -874) region of the involucrin gene promoter.
机译:整合素是角质形成细胞的角质化细胞包膜的前体蛋白之一,并在角质形成细胞分化的后期表达。干扰素-γ(IFN-γ)是一种具有抗增殖和免疫调节活性的多效细胞因子,也是鳞状细胞分化的有效诱导剂。使用培养的正常人角质形成细胞(NHK细胞)和猿猴病毒40转化的人角质形成细胞(SVHK细胞),我们研究了IFN-γ对总葡聚糖基因表达的影响。用IFN-γ(100单位/ ml)处理NHK细胞后,整合素的表达增加了约3倍。 Northern印迹分析显示IFN-γ增加了整合蛋白mRNA的表达。将人囊泡蛋白基因5'侧翼区域中的+42至-2463片段亚克隆至萤光素酶报告载体中,并将​​构建体(p2463Luc)转染至SVHK细胞中。 IFN-γ处理后,p2463Luc使荧光素酶活性增加了3倍。序列分析检测到两个推定的IFN-γ应答区域[G1(-883至-874)和G2(-784至-775)]。 p2463Luc载体的缺失分析表明,G1区对于inluclucrin基因的IFN-γ依赖性上调至关重要。凝胶位移分析显示,STAT1(信号转导和转录激活因子1)蛋白与G1区结合,并且在IFN-γ的存在下转染STAT1表达载体可提高长春菊蛋白的启动子活性。相反,STAT1显性负表达载体的转染抑制了inluclucrin启动子活性的IFN-γ依赖性上调。这些结果表明,IFN-γ通过整合素基因启动子的G1(-883至-874)区域刺激人类整合素基因的表达。

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