Key result
Grk2 keeps epithelial Na+ channels active by phosphorylating the beta subunit to prevent Nedd4-2 inhibition.
Why the study?
The regulation of epithelial Na+ channels by Grk2 and its impact on Nedd4/Nedd4-2-dependent inhibition and hypertension was previously unreported.
Does not support clinical translation; leaves open whether Grk2 modulation affects sodium handling in vivo.
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 beta 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.
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Dinudom et al. (2004) studied Hypertension. Grk2 was evaluated on Epithelial Na+ channel regulation. Grk2 phosphorylates the C terminus of the epithelial Na+ channel beta subunit, rendering the channels insensitive to inhibition by Nedd4-2 and maintaining them in an active state.
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