首页> 美国卫生研究院文献>American Journal of Physiology - Cell Physiology >Loss of NHERF-1 expression prevents dopamine-mediated Na-K-ATPase regulation in renal proximal tubule cells from rat models of hypertension: aged F344 rats and spontaneously hypertensive rats
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Loss of NHERF-1 expression prevents dopamine-mediated Na-K-ATPase regulation in renal proximal tubule cells from rat models of hypertension: aged F344 rats and spontaneously hypertensive rats

机译:NHERF-1表达的丧失会阻止多巴胺介导的高血压大鼠模型(老年F344大鼠和自发性高血压大鼠)的肾近端小管细胞中Na-K-ATPase的调节

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摘要

Dopamine decreases Na-K-ATPase (NKA) activity by PKC-dependent phosphorylation and endocytosis of the NKA α1. Dopamine-mediated regulation of NKA is impaired in aging and some forms of hypertension. Using opossum (OK) proximal tubule cells (PTCs), we demonstrated that sodium-hydrogen exchanger regulatory factor-1 (NHERF-1) associates with NKA α1 and dopamine-1 receptor (D1R). This association is required for the dopamine-mediated regulation of NKA. In OK cells, dopamine decreases NHERF-1 association with NKA α1 but increases its association with D1R. However, it is not known whether NHERF-1 plays a role in dopamine-mediated NKA regulation in animal models of hypertension. We hypothesized that defective dopamine-mediated regulation of NKA results from the decrease in NHERF-1 expression in rat renal PTCs isolated from animal models of hypertension [spontaneously hypertensive rats (SHRs) and aged F344 rats]. To test this hypothesis, we isolated and cultured renal PTCs from 22-mo-old F344 rats and their controls, normotensive 4-mo-old F344 rats, and SHRs and their controls, normotensive Wistar-Kyoto (WKY) rats. The results demonstrate that in both hypertensive models (SHR and aged F344), NHERF-1 expression, dopamine-mediated phosphorylation of NKA, and ouabain-inhibitable K+ transport are reduced. Transfection of NHERF-1 into PTCs from aged F344 and SHRs restored dopamine-mediated inhibition of NKA. These results suggest that decreased renal NHERF-1 expression contributes to the impaired dopamine-mediated inhibition of NKA in PTCs from animal models of hypertension.
机译:多巴胺通过PKC依赖性磷酸化和NKAα1的内吞作用降低Na-K-ATPase(NKA)活性。多巴胺介导的NKA调节在衰老和某些形式的高血压中受损。使用负鼠(OK)近端小管细胞(PTC),我们证明了钠氢交换调节因子1(NHERF-1)与NKAα1和多巴胺1受体(D1R)相关。多巴胺介导的NKA调节需要这种关联。在OK细胞中,多巴胺降低NHERF-1与NKAα1的缔合,但增加其与D1R的缔合。但是,尚不清楚在高血压动物模型中,NHERF-1是否在多巴胺介导的NKA调节中起作用。我们假设多巴胺介导的NKA调节缺陷是由于从高血压动物模型[自发性高血压大鼠(SHRs)和F344老龄大鼠]分离出的大鼠肾PTC中NHERF-1表达的降低引起的。为了验证该假设,我们从22个月大的F344大鼠及其对照组,血压正常的4个月大F344大鼠以及SHRs及其对照组,血压正常的Wistar-Kyoto(WKY)大鼠中分离并培养了肾PTC。结果表明,在两种高血压模型(SHR和F344年龄)中,NHERF-1表达,多巴胺介导的NKA磷酸化和哇巴因抑制性K + 转运均降低。将NHERF-1转染到来自老龄F344和SHR的PTC中,恢复了多巴胺介导的NKA抑制作用。这些结果表明,降低肾脏NHERF-1表达可导致多巴胺介导的高血压动物模型中PTC中NKA的抑制作用减弱。

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