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首页> 外文期刊>American Journal of Physiology >Epidermal growth factor regulation of rat NHE2 gene expression.
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Epidermal growth factor regulation of rat NHE2 gene expression.

机译:表皮生长因子调节大鼠NHE2基因的表达。

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Epidermal growth factor (EGF) is involved in acute regulation of Na(+)/H(+) exchangers (NHEs), but the effect of chronic EGF administration on NHE gene expression is unknown. The present studies showed that EGF treatment increased NHE2-mediated intestinal brush-border membrane vesicle Na(+) absorption and NHE2 mRNA abundance by nearly twofold in 19-day-old rats. However, no changes were observed in renal NHE2 mRNA or intestinal and renal NHE3 mRNA abundance. To understand the mechanism of this regulation, we developed the rat intestinal epithelial (RIE) cell as an in vitro model to study the effect of EGF on NHE2 gene expression. EGF increased functional NHE2 activity and mRNA abundance in cultured RIE cells, and this stimulation could be blocked by actinomycin D (a transcriptional inhibitor). Additionally, NHE2 promoter reporter gene assays in transiently transfected RIE cells showed an almost twofold increase in promoter activity after EGF treatment. We conclude that rat NHE2 activity can be stimulated by chronic EGF treatment and that this response is at least partially mediated by gene transcription.
机译:表皮生长因子(EGF)参与Na(+)/ H(+)交换子(NHEs)的急性调节,但慢性EGF施用对NHE基因表达的影响尚不清楚。本研究表明,EGF处理在19日龄大鼠中使NHE2介导的肠刷状边界膜囊泡Na(+)吸收和NHE2 mRNA丰度增加了近两倍。然而,未观察到肾脏NHE2 mRNA或肠道和肾脏NHE3 mRNA丰度的变化。为了了解这种调节的机制,我们开发了大鼠肠上皮(RIE)细胞作为体外模型,以研究EGF对NHE2基因表达的影响。 EGF增加了培养的RIE细胞的功能性NHE2活性和mRNA的丰度,这种刺激可能被放线菌素D(一种转录抑制剂)所阻断。此外,瞬时转染的RIE细胞中的NHE2启动子报告基因检测表明EGF处理后,启动子活性几乎提高了两倍。我们得出结论,慢性EGF治疗可以刺激大鼠NHE2的活性,并且这种反应至少部分地由基因转录介导。

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