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肿瘤坏死因子-α降低DJM-1角质形成细胞中水通道蛋白-3的表达。

Tumor necrosis factor-alpha decreases aquaporin-3 expression in DJM-1 keratinocytes.

作者信息

Horie Ichiro, Maeda Mamiko, Yokoyama Satoshi, Hisatsune Akinori, Katsuki Hiroshi, Miyata Takeshi, Isohama Yoichiro

机构信息

Department of Chemico-Pharmacological Sciences, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan.

出版信息

Biochem Biophys Res Commun. 2009 Sep 25;387(3):564-8. doi: 10.1016/j.bbrc.2009.07.077. Epub 2009 Jul 18.

Abstract

Aquaporin-3 (AQP3) is a water/glycerol-transporting protein that is strongly expressed at the plasma membranes of keratinocytes in skin. There is evidence for involvement of AQP3-facilitated water and glycerol transport in skin hydration and wound repair, respectively. In this study, we show that tumor necrosis factor-alpha (TNF-alpha) and TNF receptor-1 signaling decreased AQP3 protein expression and plasma membrane water permeability in DJM-1 keratinocytes. TNF-alpha also decreased AQP3 mRNA expression and promoter activity, indicating that TNF-alpha suppresses AQP3 gene transcription. In addition, inhibitors of p38 and extracellular signal-regulated kinase (ERK) abolished the effect of TNF-alpha on AQP3 expression level, whereas inhibitors for NF-kappaB did not. These data indicate that TNF-alpha decreases AQP3 gene expression through p38 and ERK activation, and suggest that the decrease in AQP3 expression caused by TNF-alpha might be related to the phenotypes of skin inflammation, such as dry skin.

摘要

水通道蛋白3(AQP3)是一种水/甘油转运蛋白,在皮肤角质形成细胞的质膜上大量表达。有证据表明,AQP3促进的水和甘油转运分别参与皮肤水合作用和伤口修复。在本研究中,我们发现肿瘤坏死因子-α(TNF-α)和TNF受体-1信号传导降低了DJM-1角质形成细胞中AQP3蛋白的表达和质膜水通透性。TNF-α还降低了AQP3 mRNA的表达和启动子活性,表明TNF-α抑制AQP3基因转录。此外,p38和细胞外信号调节激酶(ERK)抑制剂消除了TNF-α对AQP3表达水平的影响,而NF-κB抑制剂则没有。这些数据表明,TNF-α通过激活p38和ERK降低AQP3基因表达,并提示TNF-α引起的AQP3表达降低可能与皮肤炎症的表型有关,如皮肤干燥。

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