Efendiev R, Das-Panja K, Cinelli A R, Bertorello A M, Pedemonte C H
College of Pharmacy, University of Houston, 4800 Calhoun Road, Houston, TX 77204, USA.
Br J Pharmacol. 2007 Aug;151(7):1006-13. doi: 10.1038/sj.bjp.0707304. Epub 2007 May 29.
Dopamine is a major regulator of sodium reabsorption in proximal tubule epithelia. By binding to D1-receptors, dopamine induces endocytosis of plasma membrane Na,K-ATPase, resulting in a reduced capacity of the cells to transport sodium, thus contributing to natriuresis. We have previously demonstrated several aspects of the molecular mechanism by which dopamine induces Na,K-ATPase endocytosis; however, the location of intracellular compartments containing Na,K-ATPase molecules has not been identified.
In this study, we used different approaches to determine the localization of Na,K-ATPase-containing intracellular compartments. By expression of fluorescent-tagged Na,K-ATPase molecules in opossum kidney cells, a cell culture model of proximal tubule epithelia, we used fluorescence microscopy to determine cellular distribution of the fluorescent molecules and the effects of dopamine on this distribution. By labelling cell surface Na,K-ATPase molecules from the cell exterior with either biotin or an epitope-tagged antibody, we determined the localization of the tagged Na,K-ATPase molecules after endocytosis induced by dopamine.
In cells expressing fluorescent-tagged Na,K-ATPase molecules, there were intracellular compartments containing Na,K-ATPase molecules. These compartments were in very close proximity to the plasma membrane. Upon treatment of the cells with dopamine, the fluorescence labelling of these compartments was increased. The labelling of these compartments was also observed when the endocytosis of biotin- or antibody-tagged plasma membrane Na,K-ATPase molecules was induced by dopamine.
The intracellular compartments containing Na,K-ATPase molecules are located just underneath the plasma membrane.
多巴胺是近端肾小管上皮细胞钠重吸收的主要调节因子。多巴胺通过与D1受体结合,诱导质膜钠钾ATP酶的内吞作用,导致细胞转运钠的能力降低,从而促进尿钠排泄。我们之前已经证明了多巴胺诱导钠钾ATP酶内吞作用的分子机制的几个方面;然而,含有钠钾ATP酶分子的细胞内区室的位置尚未确定。
在本研究中,我们使用了不同的方法来确定含有钠钾ATP酶的细胞内区室的定位。通过在负鼠肾细胞(近端肾小管上皮细胞的一种细胞培养模型)中表达荧光标记的钠钾ATP酶分子,我们使用荧光显微镜来确定荧光分子的细胞分布以及多巴胺对这种分布的影响。通过用生物素或表位标记抗体从细胞外部标记细胞表面的钠钾ATP酶分子,我们确定了多巴胺诱导内吞作用后标记的钠钾ATP酶分子的定位。
在表达荧光标记钠钾ATP酶分子的细胞中,存在含有钠钾ATP酶分子的细胞内区室。这些区室非常靠近质膜。用多巴胺处理细胞后,这些区室的荧光标记增加。当多巴胺诱导生物素或抗体标记的质膜钠钾ATP酶分子的内吞作用时,也观察到了这些区室的标记。
含有钠钾ATP酶分子的细胞内区室位于质膜下方。