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Published as doi: 10.1096/fj.06-6046com.
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(The FASEB Journal. 2007;21:1189-1201.)
© 2007 FASEB

The A-kinase anchoring protein 15 regulates feedback inhibition of the epithelial Na+ channel

Abderrahmane Bengrine, Jinqing Li and Mouhamed S. Awayda1

Department of Physiology and Biophysics, State University of New York at Buffalo, Buffalo, New York, USA

1Correspondence: Department of Physiology and Biophysics SUNY at Buffalo 124 Sherman Hall, 3435 Main St. Buffalo, NY 14214, USA. E-mail: awayda{at}buffalo.edu

Protein kinase A anchoring proteins or AKAPs regulate the activity of many ion channels. Protein kinase A (PKA) is a well-recognized target of AKAPs, with other kinases now emerging as additional targets. We examined the roles of epithelial-expressed AKAPs in regulating the epithelial Na+ channel (ENaC). Experiments used heterologous expression with AKAP15, AKAP-KL, and AKAP79 in Xenopus oocytes. Experiments were carried out under high and low Na+ conditions, as Na+ loading is known to affect the baseline activity of ENaC in a PKC-dependent mechanism. ENaC activity was unaffected by AKAP79 and AKAP-KL expression. However, oocytes coexpressing AKAP15 exhibited an 80% and 91% reduction in the amiloride-sensitive, whole-cell conductance in high and low Na+ conditions, respectively. The reduced channel activity was unaffected by PKA activation or inhibition, indicating a PKA-independent mechanism. Expression with a membrane-targeting domain, mutant form of AKAP15 (AKAP15m) prevented the decrease of ENaC activity, but only under low Na+ conditions. In high sodium conditions, coexpression with AKAP15m led to an increase of ENaC activity to levels similar to those observed under low Na+. These results indicate that membrane-associated AKAP15 reduces ENaC activity whereas the cytoplasmically associated one may participate in the channel’s feedback inhibition by intracellular Na+, a process known to involve PKC. This hypothesis was further confirmed in coexpression experiments, which demonstrated functional and physical interaction between AKAP15 and PKC{alpha}. We propose that AKAP15 regulates ENaC via a novel PKA-independent pathway.—Bengrine, A., Li, J., Awayda, M. S. The A-kinase anchoring protein 15 regulates feedback inhibition of the epithelial Na+ channel.


Key Words: PKA • ENaC activity • intracellular Na+ • AKAP15




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