The kinase Grk2 regulates Nedd4/Nedd4-2-dependent control of epithelial Na+ channels

被引:70
作者
Dinudom, A
Fotia, AB
Lefkowitz, RJ
Young, JA
Kumar, S
Cook, DI [1 ]
机构
[1] Univ Sydney, Dept Physiol, Sydney, NSW 2006, Australia
[2] Hanson Inst, Inst Med & Vet Sci, Adelaide, SA 5000, Australia
[3] Univ Adelaide, Dept Med, Adelaide, SA 5000, Australia
[4] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[6] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
关键词
amiloricle; ubiquitin protein ligases;
D O I
10.1073/pnas.0402178101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epithelial Na+ channels mediate the transport of Na across epithelia in the kidney, gut, and lungs and are required for blood pressure regulation. They are inhibited by ubiquitin protein ligases, such as Nedd4 and Nedd4-2, with loss of this inhibition leading to hypertension. Here, we report that these channels are maintained in the active state by the G protein-coupled receptor kinase, Grk2, which has been previously implicated in the development of essential hypertension. We also show that Grk2 phosphorylates the C terminus of the channel 13 subunit and renders the channels insensitive to inhibition by Nedd4-2. This mechanism has not been previously reported to regulate epithelial Na+ channels and provides a potential explanation for the observed association of Grk2 overactivity with hypertension. Here, we report a G protein-coupled receptor kinase regulating a membrane protein other than a receptor and provide a paradigm for understanding how the interaction between membrane proteins and ubiquitin protein ligases is controlled.
引用
收藏
页码:11886 / 11890
页数:5
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