Stimulation of Xenopus oocyte Na+,K+ATPase by the serum and glucocorticoid-dependent kinase sgk1

被引:76
作者
Setiawan, I
Henke, G
Feng, YX
Böhmer, C
Vasilets, LA
Schwarz, W
Lang, F
机构
[1] Univ Tubingen, Inst Physiol, D-72076 Tubingen, Germany
[2] Univ Halle Wittenberg, Julius Bernstein Inst Physiol, Wittenberg, Germany
[3] Russian Acad Sci, Inst Chem Phys Res, Moscow, Russia
[4] Max Planck Inst Biophys, D-6000 Frankfurt, Germany
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2002年 / 444卷 / 03期
关键词
aldosterone; Na+ channels; insulin; IGF-1; kidney;
D O I
10.1007/s00424-002-0823-z
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The serum and glucocorticoid-dependent kinase-1 (sgk1) is expressed in a wide variety of tissues including renal epithelial cells. As it is up-regulated by aldosterone, it is considered to participate in the regulation of renal Na+ reabsorption. Indeed, co-expression of sgk1 with the renal epithelial Na+ channel (ENaC) augments Na+ channel activity. The aim of the present study was to examine possible effects of sgk1 on Na+/K+-ATPase activity. To this end dual-electrode voltage-clamp experiments were performed in Xenopus oocytes expressing the active kinase (S422D)sgk1 or the inactive mutant (K127N)sgk1. Na+/K+-ATPase activity was estimated from the hyperpolarization (DeltaV(m))and the outwardly-directed current (I-P) created by addition of extracellular K+ in the presence of K+ channel blocker Ba2+. Both DeltaV(m) and I-P were significantly larger in oocytes expressing (S422D)sgk1 than in those expressing (K127N)sgk1 or having been injected with water. I-P was fully inhibited by ouabain. Ion-selective microelectrodes showed that the stimulation of pump current was not the result of altered cytosolic Na+ activity or pH. The present results thus point to an additional action of sgk1 that may participate in the regulation of renal tubular Na+ transport. Moreover, sgk1 may be involved in the regulation of Na+/K+-ATPase in extrarenal tissues.
引用
收藏
页码:426 / 431
页数:6
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