Regulation of the epithelial calcium channel TRPV6 by the serum and glucocorticoid-inducible kinase isoforms SGK1 and SGK3

被引:33
|
作者
Boehmer, C. [1 ]
Palmada, M. [1 ,2 ]
Kenngott, C. [1 ]
Lindner, R. [1 ]
Klaus, F. [1 ]
Laufer, J. [1 ]
Lang, F. [1 ]
机构
[1] Univ Tubingen, Dept Physiol 1, D-72074 Tubingen, Germany
[2] Univ Duisburg Essen, Dept Mol Biol, Duisburg, Germany
关键词
calcium channel; signal transduction; protein kinase; TRPV6; SGK1;
D O I
10.1016/j.febslet.2007.11.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epithelial calcium (re) absorption is mediated by TRPV5 and TRPV6 channels. TRPV5 is modulated by the SGK1 kinase, a process requiring the PDZ-domain containing scaffold protein NHERF2. The present study explored whether TRPV6 is similarly regulated by SGKs and the scaffold proteins NHERF1/2. In Xenopus oocytes, SGKs activate TRPV6 by increasing its plasma membrane abundance. Deletion of the putative PDZ binding motif on TRPV6 did not abolish channel activation by SGKs. Furthermore, coexpression of neither NHERF1 nor NHERF2 affected TRPV6 or potentiated the SGKs stimulating effect. The present observations disclose a novel TRPV6 regulatory mechanism which presumably participates in calcium homeostasis. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:5586 / 5590
页数:5
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