Alvarez de la Rosa D, Coric T, Todorovic N, Shao D, Wang T, Canessa C M
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06520-8026, USA.
J Physiol. 2003 Sep 1;551(Pt 2):455-66. doi: 10.1113/jphysiol.2003.042903. Epub 2003 Jun 19.
The serum- and glucocorticoid-induced kinase-1 (sgk1) increases the activity of a number of epithelial ion channels and transporters. The present study examines the distribution and subcellular localization of sgk1 protein in the rat kidney and the regulation of levels of expression induced by steroids. The results indicate that the kidney expresses predominantly the sgk1 isoform with a distribution restricted to the thick ascending limb of Henle, distal convoluted, connecting and cortical collecting tubules. Within cells, sgk1 strongly associates with the microsomal fraction of homogenates and it colocalizes with the Na+,K+-ATPase to the basolateral membrane. Analysis of the levels of expression of sgk1 by Western blotting and immunohistochemistry indicates constitutive high expression under basal conditions. Approximately half of the basal level is maintained by glucocorticoids whereas physiological fluctuations of aldosterone produce minor changes in sgk1 abundance in adrenal-intact animals. These results do not support the notion that physiological changes of aldosterone concentration turn the expression of sgk1 'on and off' in the mammalian kidney. Additionally, localization of sgk1 to the basolateral membrane indicates that the effects mediated by sgk1 do not require a direct interaction with the ion channels and transporters whose activity is modulated, since most of these proteins are located in the apical membrane of renal epithelial cells.
血清和糖皮质激素诱导激酶-1(sgk1)可增强多种上皮离子通道和转运体的活性。本研究检测了sgk1蛋白在大鼠肾脏中的分布和亚细胞定位,以及类固醇诱导的表达水平调控。结果表明,肾脏主要表达sgk1异构体,其分布局限于髓袢升支粗段、远曲小管、连接小管和皮质集合管。在细胞内,sgk1与匀浆的微粒体部分紧密结合,并与Na +,K + -ATP酶共定位于基底外侧膜。通过蛋白质免疫印迹法和免疫组织化学分析sgk1的表达水平,结果表明在基础条件下sgk1呈组成性高表达。基础水平的大约一半由糖皮质激素维持,而醛固酮的生理波动在肾上腺完整的动物中对sgk1丰度产生微小变化。这些结果不支持醛固酮浓度的生理变化在哺乳动物肾脏中开启和关闭sgk1表达这一观点。此外,sgk1定位于基底外侧膜表明,sgk1介导的效应不需要与活性受调控的离子通道和转运体直接相互作用,因为这些蛋白大多数位于肾上皮细胞的顶端膜。