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醛固酮通过激活蛋白激酶D调节肾皮质集合管细胞中上皮钠通道亚基的快速转运。

Aldosterone regulates rapid trafficking of epithelial sodium channel subunits in renal cortical collecting duct cells via protein kinase D activation.

作者信息

McEneaney Victoria, Harvey Brian J, Thomas Warren

机构信息

Department of Molecular Medicine, Royal College of Surgeons in Ireland Education and Research Centre, Smurfit Building, Beaumont Hospital, Dublin 9, Ireland.

出版信息

Mol Endocrinol. 2008 Apr;22(4):881-92. doi: 10.1210/me.2007-0225. Epub 2008 Jan 17.

Abstract

Aldosterone elicits rapid physiological responses in target tissues such as the distal nephron through the stimulation of cell signaling cascades. We identified protein kinase D (PKD1) as an early signaling response to aldosterone treatment in the M1-cortical collecting duct (M1-CCD) cell line. PKD1 activation was blocked by the PKC inhibitor chelerythrine chloride and by rottlerin, a specific inhibitor of PKCdelta. The activation of PKCdelta and PKCepsilon coincided with PKD1 activation and while a complex was formed between PKD1 and PKCepsilon after aldosterone treatment, there was a concurrent reduction in PKD1 association with PKCdelta. A stable PKD1 knockdown M1-CCD-derrived clone was developed in which PKD1 expression was 90% suppressed by gene silencing with a PKD1-specific siRNA. The effect of aldosterone treatment on the subcellular distribution of enhanced cyan fluorescent protein (eCFP)-tagged epithelial sodium channel (ENaC) subunits in wild type (WT) and PKD1 suppressed cells was examined using confocal microscopy. In an untreated confluent monolayer of M1-CCD cells, alpha, beta, and gamma ENaC subunits were evenly distributed throughout the cytoplasm of WT and PKD1-suppressed cells. After 2 min treatment, aldosterone stimulated the localization of each of the ENaC subunits to discrete regions within the cytoplasm of WT cells. The translocation of eCFP-ENaC subunits in WT cells was inhibited by rottlerin and the mineralocorticoid receptor (MR) antagonist spironolactone. No subcellular translocation of eCFP-ENaC subunits was observed in PKD1-suppressed cells treated with aldosterone. These data demonstrate the involvement of a novel MR/PKCdelta /PKD1 signaling cascade in the earliest ENaC subunit intracellular trafficking events that follow aldosterone treatment.

摘要

醛固酮通过刺激细胞信号级联反应,在诸如远端肾单位等靶组织中引发快速的生理反应。我们确定蛋白激酶D(PKD1)是M1型皮质集合管(M1-CCD)细胞系中对醛固酮处理的早期信号反应。PKD1的激活被蛋白激酶C(PKC)抑制剂氯化白屈菜红碱以及PKCδ的特异性抑制剂罗特lerin阻断。PKCδ和PKCε的激活与PKD1的激活同时发生,并且在醛固酮处理后PKD1与PKCε之间形成了复合物,而PKD1与PKCδ的结合同时减少。构建了一个稳定的PKD1敲低的M1-CCD衍生克隆,其中通过用PKD1特异性小干扰RNA(siRNA)进行基因沉默,PKD1表达被抑制了90%。使用共聚焦显微镜检查了醛固酮处理对野生型(WT)和PKD1抑制细胞中增强型青色荧光蛋白(eCFP)标记的上皮钠通道(ENaC)亚基亚细胞分布的影响。在未处理的汇合单层M1-CCD细胞中,α、β和γ ENaC亚基均匀分布在WT和PKD1抑制细胞的整个细胞质中。处理2分钟后,醛固酮刺激每个ENaC亚基定位到WT细胞细胞质内的离散区域。WT细胞中eCFP-ENaC亚基的易位被罗特lerin和盐皮质激素受体(MR)拮抗剂螺内酯抑制。在用醛固酮处理的PKD1抑制细胞中未观察到eCFP-ENaC亚基的亚细胞易位。这些数据证明了一种新的MR/PKCδ/PKD1信号级联参与了醛固酮处理后最早的ENaC亚基细胞内运输事件。

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