Regulation of Chloride Channel Trafficking by Cyclic AMP via Protein Kinase A-Independent Pathway in A6 Renal Epithelial Cells

• Published in: Biochemical and biophysical research communications Vol. 223; no. 2; pp. 234 - 239
• Main Authors: Shintani, Yutaka, Marunaka, Yoshinori
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 14.06.1996
• Subjects: 8-Bromo Cyclic Adenosine Monophosphate - pharmacology; Animals; Brefeldin A; Cell Line; Chloride Channels - drug effects; Chloride Channels - physiology; Cyclic AMP - metabolism; Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors; Cyclopentanes - pharmacology; Enzyme Inhibitors - pharmacology; Epithelium; Ion Channel Gating - drug effects; Isoquinolines - pharmacology; Kidney; Kinetics; Patch-Clamp Techniques; Sulfonamides
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1006/bbrc.1996.0877

The apical membrane of renal epithelial A6 cells has 3 and 8 pS Cl−channels. Both types of the channels were blocked by NPPB (5-Nitro-2-(3-phenylpropylamino)-benzoic acid; 100 μM). 8-bromo-cAMP (Br-cAMP) increased the open probability of 3 pS Cl−channel and this action was inhibited by pretreatment with H89, an inhibitor of cAMP-dependent protein kinase (PKA). On the other hand, the number of 8 pS Cl−channel was increased by Br-cAMP. The increase in number of 8 pS Cl−channel by Br-cAMP was inhibited by brefeldin A (a blocker of movement of membrane protein from an intracellular pool to the cell surface) but not by H89. These observations indicate that cAMP could activate the 3 pS Cl−channel through PKA-dependent phosphorylation, and that cAMP could stimulate translocation of the 8 pS Cl−channel through PKA-independent pathways. We conclude that PKA-independent pathways are involved in cAMP signaling mechanisms in addition to PKA-dependent pathways.