University of Arizona Health Sciences Center, Tucson, Arizona 85724, USA.
Am J Physiol Cell Physiol. 2010 Jul;299(1):C51-7. doi: 10.1152/ajpcell.00081.2010. Epub 2010 Apr 7.
Sodium/hydrogen exchangers (NHEs) play a major role in Na(+) absorption, cell volume regulation, and intracellular pH regulation. Of the nine identified mammalian NHEs, three (NHE2, NHE3, and NHE8) are localized on the apical membrane of epithelial cells in the small intestine and the kidney. Although the regulation of NHE2 and NHE3 expression has been extensively studied in the past decade, little is known about the regulation of NHE8 gene expression under physiological conditions. The current studies were performed to explore the role of epidermal growth factor (EGF) on NHE8 expression during intestinal maturation. Brush-border membrane vesicles (BBMV) were isolated from intestinal epithelia, and Western blot analysis was performed to determine NHE8 protein expression of sucking male rats treated with EGF. Real-time PCR was used to quantitate NHE8 mRNA expression in rats and Caco-2 cells. Human NHE8 promoter activity was characterized through transfection of Caco-2 cells. Gel mobility shift assays (GMSAs) were used to identify the promoter sequences and the transcriptional factors involved in EGF-mediated regulation. Our results showed that intestinal NHE8 mRNA expression was decreased in EGF-treated rats and Caco-2 cells, and NHE8 protein abundance was also decreased in EGF-treated rats. The activity of the human NHE8 gene promoter transfected in Caco-2 cells was also reduced by EGF treatment. This could be explained by reduced binding of transcription factor Sp3 on the NHE8 basal promoter region in the presence of EGF. Pretreatment with MEK1/2 inhibitor UO-126 could prevent EGF-mediated inhibition of NHE8 gene expression. In conclusion, this study showed that EGF inhibits NHE8 gene expression through reducing its basal transcription, suggesting an important role of EGF in regulating NHE expression during intestinal maturation.
钠离子/氢交换器(NHEs)在钠离子吸收、细胞体积调节和细胞内 pH 调节中起主要作用。在鉴定出的 9 种哺乳动物 NHE 中,有 3 种(NHE2、NHE3 和 NHE8)定位于小肠和肾脏上皮细胞的顶膜上。尽管在过去十年中已经广泛研究了 NHE2 和 NHE3 表达的调节,但对于生理条件下 NHE8 基因表达的调节知之甚少。目前的研究旨在探讨表皮生长因子(EGF)在肠道成熟过程中对 NHE8 表达的作用。从小肠上皮细胞中分离出刷状缘膜囊泡(BBMV),并通过 Western blot 分析确定接受 EGF 处理的雄性吸吮大鼠的 NHE8 蛋白表达。实时 PCR 用于定量大鼠和 Caco-2 细胞中的 NHE8 mRNA 表达。通过转染 Caco-2 细胞来表征人 NHE8 启动子活性。凝胶迁移率变动分析(GMSAs)用于鉴定 EGF 介导调节所涉及的启动子序列和转录因子。我们的结果表明,EGF 处理会降低大鼠和 Caco-2 细胞中的肠道 NHE8 mRNA 表达,并且 NHE8 蛋白丰度也会降低。转染 Caco-2 细胞的人 NHE8 基因启动子活性也会因 EGF 处理而降低。这可以通过 EGF 存在时转录因子 Sp3 对 NHE8 基础启动子区域的结合减少来解释。用 MEK1/2 抑制剂 UO-126 预处理可以阻止 EGF 介导的 NHE8 基因表达抑制。总之,这项研究表明,EGF 通过降低其基础转录来抑制 NHE8 基因表达,表明 EGF 在肠道成熟过程中调节 NHE 表达中起重要作用。