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

被引:39
作者
Horie, Ichiro [1 ]
Maeda, Mamiko [1 ]
Yokoyama, Satoshi [1 ]
Hisatsune, Akinori [1 ]
Katsuki, Hiroshi [1 ]
Miyata, Takeshi [2 ]
Isohama, Yoichiro [1 ]
机构
[1] Kumamoto Univ, Dept Chemicopharmacol Sci, Grad Sch Pharmaceut Sci, Kumamoto 8620973, Japan
[2] Sojo Univ, Fac Pharmaceut Sci, Lab Presymptomat Med Pharmacol, Kumamoto 8600082, Japan
关键词
Aquaporin-3; TNF-alpha; Gene expression; Keratinocytes; MAP kinases; MEMBRANE WATER PERMEABILITY; STRATUM-CORNEUM HYDRATION; LUNG EPITHELIAL-CELLS; FACTOR-KAPPA-B; TNF-ALPHA; SKIN; GLYCEROL; CHANNELS; MICE;
D O I
10.1016/j.bbrc.2009.07.077
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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-kappa B 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. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:564 / 568
页数:5
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