Department of Anesthesiology and Perioperative Medicine, Georgia Regents University, Augusta, Georgia;
Center for Lung Biology, University of South Alabama, Mobile, Alabama; Department of Pharmacology, University of South Alabama, Mobile, Alabama; and.
Am J Physiol Cell Physiol. 2014 Oct 1;307(7):C648-56. doi: 10.1152/ajpcell.00210.2014. Epub 2014 Aug 6.
The low-voltage-activated T-type Ca(2+) channels play an important role in mediating the cellular responses to altered oxygen tension. Among three T-type channel isoforms, α1G, α1H, and α1I, only α1H was found to be upregulated under hypoxia. However, mechanisms underlying such hypoxia-dependent isoform-specific gene regulation remain incompletely understood. We, therefore, studied the hypoxia-dependent transcriptional regulation of α1G and α1H gene promoters with the aim to identify the functional hypoxia-response elements (HREs). In rat pulmonary artery smooth muscle cells (PASMCs) and pheochromocytoma (PC12) cells after hypoxia (3% O2) exposure, we observed a prominent increase in α1H mRNA at 12 h along with a significant rise in α1H-mediated T-type current at 24 and 48 h. We then cloned two promoter fragments from the 5'-flanking regions of rat α1G and α1H gene, 2,000 and 3,076 bp, respectively, and inserted these fragments into a luciferase reporter vector. Transient transfection of PASMCs and PC12 cells with these recombinant constructs and subsequent luciferase assay revealed a significant increase in luciferase activity from the reporter containing the α1H, but not α1G, promoter fragment under hypoxia. Using serial deletion and point mutation analysis strategies, we identified a functional HRE at site -1,173cacgc-1,169 within the α1H promoter region. Furthermore, an electrophoretic mobility shift assay using this site as a DNA probe demonstrated an increased binding activity to nuclear protein extracts from the cells after hypoxia exposure. Taken together, these findings indicate that hypoxia-induced α1H upregulation involves binding of hypoxia-inducible factor to an HRE within the α1H promoter region.
低电压激活的 T 型钙(Ca2+)通道在调节细胞对氧张力变化的反应中发挥重要作用。在三种 T 型通道同工型中,α1G、α1H 和 α1I,只有α1H 被发现在低氧条件下上调。然而,这种缺氧依赖性同工型特异性基因调控的机制仍不完全清楚。因此,我们研究了α1G 和α1H 基因启动子的缺氧依赖性转录调控,目的是确定功能性缺氧反应元件(HRE)。在低氧(3% O2)暴露后的大鼠肺动脉平滑肌细胞(PASMCs)和嗜铬细胞瘤(PC12)细胞中,我们观察到α1H mRNA 在 12 小时时明显增加,同时在 24 和 48 小时时α1H 介导的 T 型电流显著增加。然后,我们从大鼠α1G 和α1H 基因的 5'-侧翼区分别克隆了两个启动子片段,长度分别为 2000 和 3076 个碱基对,并将这些片段插入到荧光素酶报告载体中。瞬时转染 PASMCs 和 PC12 细胞,用这些重组构建体进行荧光素酶测定,结果显示,在低氧条件下,含有α1H 启动子片段的报告基因的荧光素酶活性显著增加,但含有α1G 启动子片段的报告基因则没有。通过串联缺失和点突变分析策略,我们在α1H 启动子区域的 -1,173cacgc-1,169 位点鉴定出一个功能性 HRE。此外,使用该位点作为 DNA 探针的电泳迁移率变动分析显示,低氧暴露后细胞的核蛋白提取物与该位点的结合活性增加。综上所述,这些发现表明,缺氧诱导的α1H 上调涉及缺氧诱导因子与α1H 启动子区域内的 HRE 结合。