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首页> 外文期刊>American Journal of Physiology >HIF-1 regulates hypoxic induction of NHE1 expression and alkalinization of intracellular pH in pulmonary arterial myocytes.
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HIF-1 regulates hypoxic induction of NHE1 expression and alkalinization of intracellular pH in pulmonary arterial myocytes.

机译:HIF-1调节肺动脉心肌细胞中NHE1表达的缺氧诱导和细胞内pH的碱化。

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Vascular remodeling resulting from altered pulmonary arterial smooth muscle cell (PASMC) growth is a contributing factor to the pathogenesis of hypoxic pulmonary hypertension. PASMC growth requires an alkaline shift in intracellular pH (pH(i)) and we previously showed that PASMCs isolated from mice exposed to chronic hypoxia exhibited increased Na(+)/H(+) exchanger (NHE) expression and activity, which resulted in increased pH(i). However, the mechanism by which hypoxia caused these changes was unknown. In this study we tested the hypothesis that hypoxia-induced changes in PASMC pH homeostasis are mediated by the transcriptional regulator hypoxia-inducible factor 1 (HIF-1). Consistent with previous results, increased NHE isoform 1 (NHE1) mRNA and protein, enhanced NHE activity, and an alkaline shift in pH(i) were observed in PASMCs isolated from wild-type mice exposed to chronic hypoxia (3 wk at 10% O(2)). In contrast, these changes were absent in PASMCs isolated from chronically hypoxic mice with partial deficiency for HIF-1. Exposure of PASMCs to hypoxia ex vivo (48 h at 4% O(2)) or overexpression of HIF-1 in the absence of hypoxia also increased NHE1 mRNA and protein expression. Our results indicate that full expression of HIF-1 is essential for hypoxic induction of NHE1 expression and changes in PASMC pH homeostasis and suggest a novel mechanism by which HIF-1 mediates pulmonary vascular remodeling during the pathogenesis of hypoxic pulmonary hypertension.
机译:由改变的肺动脉平滑肌细胞(PASMC)的生长引起的血管重塑是低氧性肺动脉高压发病机制的一个重要因素。 PASMC的生长需要细胞内pH值(pH(i))发生碱性变化,我们之前的研究表明,从暴露于慢性低氧的小鼠中分离出的PASMCs具有增加的Na(+)/ H(+)交换子(NHE)表达和活性,从而导致pH(i)增加。但是,低氧引起这些变化的机制尚不清楚。在这项研究中,我们测试了以下假设:缺氧诱导的PASMC pH稳态变化是由转录调节因子缺氧诱导因子1(HIF-1)介导的。与以前的结果一致,在从暴露于慢性低氧(3 wk,10%O的野生型小鼠)中分离出的PASMC中,观察到NHE亚型1(NHE1)mRNA和蛋白增加,NHE活性增强和pH(i)发生碱性变化。 (2))。相比之下,从部分缺氧HIF-1的慢性低氧小鼠中分离出的PASMC中则没有这些变化。 PASMCs体外暴露于缺氧状态(在4%O(2)下处于48 h)或在缺氧不存在的情况下HIF-1的过度表达也会增加NHE1 mRNA和蛋白质表达。我们的结果表明,HIF-1的完整表达对于NHE1的低氧诱导和PASMC pH稳态的改变是必不可少的,并暗示了HIF-1在低氧性肺动脉高压发病过程中介导肺血管重构的新机制。

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