REGULATION OF EPITHELIAL Na⁺ CHANNELS BY ALDOSTERONE: ROLE OF Sgk1

Authors: Lee, Il-Ha; Campbell, Craig R; Cook, David I; Dinudom, Anuwat

Source: Clinical and Experimental Pharmacology and Physiology, Volume 35, Number 2, February 2008 , pp. 235-241(7)

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Abstract:

SUMMARY

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The epithelial sodium channel (ENaC) is tightly regulated by hormonal and humoral factors, including cytosolic ion concentration and glucocorticoid and mineralocorticoid hormones. Many of these regulators of ENaC control its activity by regulating its surface expression via neural precursor cell-expressed developmentally downregulated (gene 4) protein (Nedd4-2).

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During the early phase of aldosterone action, Nedd4-2-dependent downregulation of ENaC is inhibited by the serum- and glucocorticoid-induced kinase 1 (Sgk1).

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Sgk1 phosphorylates Nedd4-2. Subsequently, phosphorylated Nedd4-2 binds to the 14-3-3 protein and, hence, reduces binding of Nedd4-2 to ENaC.

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Nedd4-2 is also phosphorylated by protein kinase B (Akt1). Both Sgk1 and Akt1 are part of the insulin signalling pathway that increases transepithelial Na⁺ absorption by inhibiting Nedd4-2 and activating ENaC.

Keywords: Akt; epithelial sodium channel; G-protein coupled receptor kinase 2 (Grk2); Nedd4-2; serum- and glucocorticoid-induced kinase 1 (Sgk1)

Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1440-1681.2007.04844.x

Publication date: 2008-02-01