首页> 美国卫生研究院文献>Biochemical Journal >Thapsigargin suppresses phorbol ester-dependent human involucrin promoter activity by suppressing CCAAT-enhancer-binding protein alpha (C/EBPalpha) DNA binding.
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Thapsigargin suppresses phorbol ester-dependent human involucrin promoter activity by suppressing CCAAT-enhancer-binding protein alpha (C/EBPalpha) DNA binding.

机译:Thapsigargin通过抑制CCAAT-增强子结合蛋白α(C / EBPalpha)DNA结合抑制依赖佛波酯的人Involucrin启动子活性。

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摘要

Human involucrin (hINV) is a keratinocyte differentiation marker expressed in the suprabasal epidermal layers. In cultured keratinocytes hINV mRNA levels are increased 10-fold by a 24-h treatment with 50 ng/ml PMA, an agent that promotes keratinocyte differentiation. Previous studies show that thapsigargin (TGN), an agent that depletes intracellular calcium stores, inhibits keratinocyte differentiation. In the present study we show that TGN inhibits the PMA-dependent, differentiation-associated, increase in hINV mRNA levels and hINV promoter activity. Inhibition is half-maximal at 10 nM and maximal at 100 nM TGN. Neither basal hINV promoter activity nor glyceraldehyde-3-phosphate dehydrogenase mRNA levels are inhibited. Mutation of a functionally important CAATT-enhancer-binding protein (C/EBP) site within the hINV promoter proximal regulatory region eliminates the regulation, suggesting that TGN may effect C/EBP-dependent promoter activation. Consistent with this hypothesis, TGN inhibits C/EBPalpha-dependent promoter activation via a mechanism that involves inhibition of C/EBPalpha binding to DNA without changing C/EBPalpha protein levels. These results suggest that TGN interferes with hINV expression by interfering with C/EBP transcription-factor function.
机译:人整合素(hINV)是在基底上表皮层中表达的角质形成细胞分化标记。在培养的角质形成细胞中,通过用50 ng / ml PMA(一种促进角质形成细胞分化的试剂)进行24小时处理,hINV mRNA水平增加了10倍。先前的研究表明,thapsigargin(TGN)是一种消耗细胞内钙存储的药物,可抑制角质形成细胞的分化。在本研究中,我们显示TGN抑制了hMAV依赖性,分化相关的hINV mRNA水平和hINV启动子活性的增加。抑制在10 nM时为最大值的一半,在100 nM TGN时为最大值。基本的hINV启动子活性和甘油醛-3-磷酸脱氢酶mRNA水平均不受抑制。 hINV启动子近端调节区内功能上重要的CAATT增强子结合蛋白(C / EBP)位点的突变消除了调节作用,表明TGN可能影响C / EBP依赖性启动子激活。与该假设一致,TGN通过一种机制抑制C / EBPalpha依赖性启动子的激活,该机制涉及抑制C / EBPalpha与DNA的结合而不改变C / EBPalpha蛋白的水平。这些结果表明,TGN通过干扰C / EBP转录因子功能来干扰hINV表达。

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