The Role of NHERF and E3KARP in the cAMP-mediated Inhibition of NHE3

NHE3 is the apically located Na+/H+ exchanger in the gut and in the renal proximal tubule. Acute inhibition of this transporter by cAMP requires the presence of either of two NHE3-associated proteins, NHERF or E3KARP. It has been suggested that these proteins either directly regulate NHE3 activity a...

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Bibliographic Details
Published in:The Journal of biological chemistry 1998-11, Vol.273 (45), p.29972-29978
Main Authors: Lamprecht, Georg, Weinman, Edward J., Yun, C.-H. Chris
Format: Article
Language:English
Subjects:
8-Bromo Cyclic Adenosine Monophosphate - pharmacology
Animals
Cell Line
Cyclic AMP - metabolism
Cyclic AMP-Dependent Protein Kinase Type II
Cyclic AMP-Dependent Protein Kinases - metabolism
Cytoskeletal Proteins
Enzyme Activation
Hydrogen-Ion Concentration
Opossums
Phosphoproteins - metabolism
Phosphorylation
Protein Binding
Proteins - metabolism
Sodium-Hydrogen Exchangers - antagonists & inhibitors
Sodium-Hydrogen Exchangers - metabolism
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Summary:NHE3 is the apically located Na+/H+ exchanger in the gut and in the renal proximal tubule. Acute inhibition of this transporter by cAMP requires the presence of either of two NHE3-associated proteins, NHERF or E3KARP. It has been suggested that these proteins either directly regulate NHE3 activity after being phosphorylated by protein kinase A (PKA) or that they may serve as adapters that localize PKA near NHE3. We studied the role of NHERF and E3KARP in opossum kidney cells, which endogenously express NHE3, NHERF, and ezrin and display cAMP-dependent inhibition of NHE3. In vivophosphorylation studies showed that NHERF is a phosphoprotein under basal conditions, but does not change its phosphorylation state after 8-bromo-cAMP treatment, and that E3KARP is not phosphorylated at all. Co-immunoprecipitation showed that NHERF and E3KARP bind both NHE3 and ezrin. Using cAMP analogs it was demonstrated that NHE3 activity, measured as sodium-dependent recovery of the intracellular pH after intracellular acidification, is inhibited by PKA type II. Because others have shown that ezrin binds PKA type II and that NHE3 is phosphorylated by PKA we suggest that NHERF and E3KARP are adapters that link NHE3 to ezrin, thereby localizing PKA near NHE3 to allow NHE3 phosphorylation.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.273.45.29972