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Low salt concentrations activate AMP-activated protein kinase in mouse macula densa cells

¹The Burnet Research Institute and ²Department of Nephrology, Austin Health, Heidelberg; ³St. Vincent's Institute of Medical Research, St. Vincent's Hospital, Fitzroy; and ⁴Commonwealth Scientific and Industrial Research Organisation Molecular and Health Technologies, Parkville, Victoria, Australia

Submitted 17 June 2008 ; accepted in final form 22 January 2009

The energy-sensing kinase AMP-activated protein kinase (AMPK) is associated with the sodium-potassium-chloride cotransporter NKCC2 in the kidney and phosphorylates it on a regulatory site in vitro. To identify a potential role for AMPK in salt sensing at the macula densa, we have used the murine macula densa cell line MMDD1. In this cell line, AMPK was rapidly activated by isosmolar low-salt conditions. In contrast to the known salt-sensing pathway in the macula densa, AMPK activation occurred in the presence of either low sodium or low chloride and was unaffected by inhibition of NKCC2 with bumetanide. Assays using recombinant AMPK demonstrated activation of an upstream kinase by isosmolar low salt. The specific calcium/calmodulin-dependent kinase kinase inhibitor STO-609 failed to suppress AMPK activation, suggesting that it was not part of the signal pathway. AMPK activation was associated with increased phosphorylation of the specific substrate acetyl-CoA carboxylase (ACC) at Ser⁷⁹, as well as increased NKCC2 phosphorylation at Ser¹²⁶. AMPK activation due to low salt concentrations was inhibited by an adenovirus construct encoding a kinase dead mutant of AMPK, leading to reduced ACC Ser⁷⁹ and NKCC2 Ser¹²⁶ phosphorylation. This work demonstrates that AMPK activation in macula densa-like cells occurs via isosmolar changes in sodium or chloride concentration, leading to phosphorylation of ACC and NKCC2. Phosphorylation of these substrates in vivo is predicted to increase intracellular chloride and so reduce the effect of salt restriction on tubuloglomerular feedback and renin secretion.

AMPK; NKCC2; phosphorylation; sodium reabsorption