RACK1 associates with NHE5 in focal adhesions and positively regulates the transporter activity

被引:31
|
作者
Onishi, Ichiro [1 ]
Lin, Paulo J. C. [1 ]
Diering, Graham H. [1 ]
Williams, Warren P. [1 ]
Numata, Masayuki [1 ]
机构
[1] Univ British Columbia, Biomed Res Ctr, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
基金
加拿大健康研究院;
关键词
ion homeostasis; scaffold signaling proteins; protein-protein interaction; focal adhesion;
D O I
10.1016/j.cellsig.2006.06.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Na+/H+ exchanger isoform 5 (NHE5) is a brain-enriched NHE that may play important roles in ion homeostasis and cell-volume regulation. However, the regulation mechanism of NHE5 has not been fully elucidated. Here, we show that Receptor for Activated C-kinase 1 (RACK1) directly binds to NHE5 and positively regulates the transporter function. NHE5 co-localized with RACK1 as well as beta 1 integrin, paxillin and vinculin, suggesting that NHE5 associates with focal adhesions. By using RACK1 dominant-negative mutants and siRNA, we further show that RACK1 regulates NHE5 both directly and through an integrin-dependent pathway. The NHE5-RACK1 interaction, but not the RACK1-beta 1 integrin interaction, was reinforced when cells were spread on an integrin-substrate fibronectin. We propose that RACK1 activates NHE5 both by integrin-dependent and independent pathways, which may coordinate cellular ion homeostasis during cell-matrix adhesion. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:194 / 203
页数:10
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