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维甲酸在人HaCaT角质形成细胞中诱导TR4孤儿受体的产生。

Induction of TR4 orphan receptor by retinoic acid in human HaCaT keratinocytes.

作者信息

Inui S, Lee Y F, Haake A R, Goldsmith L A, Chang C

机构信息

Department of Pathology, University of Rochester Medical Center, New York, USA.

出版信息

J Invest Dermatol. 1999 Apr;112(4):426-31. doi: 10.1046/j.1523-1747.1999.00548.x.

Abstract

Human TR4 orphan receptor (TR4) can modulate the transcriptional activity of the reporter gene containing an AGGTCA direct repeat-hormone response element. Here we studied the potential role of TR4 in human HaCaT keratinocytes. Using a chloramphenicol acetyl-transferase reporter gene assay, it was shown that TR4 can suppress retinoic acid-induced transactivation by 47.3% in human HaCaT keratinocytes. Electrophoretic mobility shift assay indicated that this suppression may be due to TR4 binding with higher affinity to the retinoic acid response element than retinoid receptors. Western blot analysis further suggested that retinoic acid can increase the expression of TR4 protein in human HaCaT keratinocytes, indicating that TR4 acts as a negative feedback modulator for retinoic acid action. Interestingly, TR4 expression is increased in normal human keratinocytes when substituting a low calcium medium with a high calcium medium. Together, our data suggested, for the first time, that an orphan receptor, such as TR4, may play an important part in retinoid-mediated signaling pathways in human keratinocytes, providing a new insight into keratinocyte biology.

摘要

人类TR4孤儿受体(TR4)可调节含有AGGTCA直接重复序列-激素反应元件的报告基因的转录活性。在此,我们研究了TR4在人HaCaT角质形成细胞中的潜在作用。通过氯霉素乙酰转移酶报告基因检测表明,在人HaCaT角质形成细胞中,TR4可使视黄酸诱导的反式激活作用抑制47.3%。电泳迁移率变动分析表明,这种抑制作用可能是由于TR4与视黄酸反应元件的结合亲和力高于类视黄醇受体。蛋白质印迹分析进一步表明,视黄酸可增加人HaCaT角质形成细胞中TR4蛋白的表达,这表明TR4作为视黄酸作用的负反馈调节因子。有趣的是,当用高钙培养基替代低钙培养基时,正常人角质形成细胞中TR4的表达会增加。总之,我们的数据首次表明,诸如TR4这样的孤儿受体可能在人角质形成细胞的类视黄醇介导的信号通路中发挥重要作用,为角质形成细胞生物学提供了新的见解。

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