Up-Regulation of Kir2.1 (KCNJ2) by the Serum & Glucocorticoid Inducible SGK3

Cellular Physiology and Biochemistry

关键词: KCNJ2;    SGK3;    Cell membrane potential;    Neurons;    Cardiomyocytes;    Heart;   

DOI  :  10.1159/000358629

学科分类：分子生物学，细胞生物学和基因

来源: S Karger AG

【 摘 要 】

Background/Aims The serum & glucocorticoid inducible kinase SGK3, an ubiquitously expressed serine/threonine kinase, regulates a variety of ion channels. It has previously been shown that SGK3 upregulates the outwardly rectifying K⁺ channel K_V11.1, which is expressed in cardiomyocytes. Cardiomyocytes further express the inward rectifier K⁺ channel K_ir2.1, which contributes to maintenance of resting cell membrane potential. Loss-of-function mutations of KCNJ2 encoding K_ir2.1 result in Andersen-Tawil syndrome with periodic paralysis, cardiac arrhythmia and dysmorphic features. The present study explored whether SGK3 participates in the regulation of K_ir2.1. Methods cRNA encoding K_ir2.1 was injected into Xenopus oocytes with and without additional injection of cRNA encoding wild type SGK3, constitutively active ^S419DSGK3 or inactive ^K191NSGK3. K_ir2.1 activity was determined by two-electrode voltage-clamp and K_ir2.1 protein abundance in the cell membrane by immunostaining and subsequent confocal imaging or by chemiluminescence. Results Injection of 10 ng cRNA encoding wild type SGK3 and ^S419DSGK3, but not ^K191NSGK3 significantly enhanced K_ir2.1-mediated currents. SGK inhibitor EMD638683 (50 µM) abrogated ^S419DSGK3-induced up-regulation of K_ir2.1. Moreover, wild type SGK3 enhanced the channel protein abundance in the cell membrane. The decay of K_ir2.1-mediated currents following inhibition of channel insertion into the cell membrane by brefeldin A (5 µM) was similar in oocytes coexpressing K_ir2.1 and SGK3 as in oocytes expressing K_ir2.1 alone, suggesting that SGK3 influences channel insertion into rather than channel retrieval from the cell membrane. Conclusions SGK3 is a novel regulator of K_ir2.1.

【 授权许可】

CC BY-NC-ND