Oxygen-dependent regulation of aquaporin-3 expression

D. Hoogewijs, Melanie Vogler, Eveline Zwenger, Sabine Krull, A. Zieseniss
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引用次数: 16

Abstract

The purpose of this study was to investigate whether aquaporin-3 (AQP3) expression is altered in hypoxia and whether hypoxia-inducible transcription factor (HIF)-1 regulates the hypoxic expression. AQP3 mRNA expression was studied in L929 fibrosarcoma cells and in several tissues derived from mice that were subjected to hypoxia. Computational analysis of the AQP3 promoter revealed conserved HIF binding sites within close proximity to the translational start site, and chromatin immunoprecipitation assays confirmed binding of HIF-1α to the endogenous hypoxia response elements. Furthermore, hypoxia resulted in increased expression of AQP3 mRNA in L929 fibrosarcoma cells. Consistently, shRNA-mediated knockdown of HIF-1α greatly reduced the hypoxic induction of AQP3. In addition, mRNA analysis of organs from mice exposed to inspiratory hypoxia demonstrated pronounced hypoxia-inducible expression of AQP3 in the kidney. Overall, our findings suggest that AQP3 expression can be regulated at the transcriptional level and that AQP3 represents a novel HIF-1 target gene.
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水通道蛋白-3表达的氧依赖性调控
本研究旨在探讨缺氧条件下水通道蛋白-3 (AQP3)的表达是否发生改变,以及缺氧诱导转录因子(HIF)-1是否调控缺氧条件下的表达。研究了缺氧小鼠的L929纤维肉瘤细胞和几种组织中AQP3 mRNA的表达。AQP3启动子的计算分析显示,在翻译起始位点附近有保守的HIF结合位点,染色质免疫沉淀试验证实了HIF-1α与内源性缺氧反应元件的结合。此外,缺氧导致L929纤维肉瘤细胞AQP3 mRNA表达增加。与此一致,shrna介导的HIF-1α的下调大大降低了AQP3的缺氧诱导。此外,对吸入性缺氧小鼠器官的mRNA分析显示,肾脏中AQP3的表达明显受缺氧诱导。总之,我们的研究结果表明,AQP3的表达可以在转录水平上受到调控,AQP3代表了一种新的HIF-1靶基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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期刊最新文献
Abstract IA-015: Hypoxia-induced SETX links replication stress with the unfolded protein response Abstract PO-033: Papaverine derivative smv-32 alleviates tumor hypoxia and radiosensitizes tumors by inhibiting mitochondrial metabolism Abstract PO-034: Changes in cancer associated fibroblast subsets following angiotensin II type I receptor blocker (ARB) treatment reduces transient hypoxia and radiation resistance Abstract IA-017: Chromatin and gene transcription in hypoxia Abstract IA-016: Metabolic deregulation drives a redox vulnerability in pancreatic cancer
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