Protein kinase C regulates urea permeability in the rat inner medullary collecting duct

• Published in: American Journal of Physiology - Renal Physiology 2010-12, Vol.299 (6), p.F1401-F1406
• Main Authors: Wang, Yanhua, Klein, Janet D, Liedtke, Carole M, Sands, Jeff M
• Format: Article
• Language: English
• Subjects: Acetophenones - pharmacology; Animals; Benzophenanthridines - pharmacology; Benzopyrans - pharmacology; Calcium; Cells; Hormones; Kidney Tubules, Collecting - drug effects; Kidney Tubules, Collecting - metabolism; Kinases; Male; Membrane Transport Proteins - metabolism; Osmolar Concentration; Permeability; Phorbol 12,13-Dibutyrate - pharmacology; Phosphorylation; Protein Kinase C - antagonists & inhibitors; Protein Kinase C - metabolism; Rats; Rats, Sprague-Dawley; Studies; Urea - metabolism; Urea Transporters; Vasopressins - pharmacology
• ISSN: 1931-857X; 0363-6127; 1522-1466
• DOI: 10.1152/ajprenal.00322.2010

Hypertonicity increases urea transport independently of, as well as synergistically with, vasopressin in the inner medullary collect duct (IMCD). We previously showed that hypertonicity does not increase the level of cAMP in the IMCD, but it does increase the level of intracellular calcium. Since we also showed that hypertonicity increases both the phosphorylation and biotinylation of the urea transporters UT-A1 and UT-A3, this would suggest involvement of a calcium-dependent protein kinase in the regulation of urea transport in the inner medulla. In this study, we investigated whether protein kinase C (PKC), which is present in the IMCD, is a regulator of urea permeability. We tested the effect of PKC inhibitors and activators on urea permeability in the isolated, perfused rat terminal IMCD. Increasing osmolality from 290 to 690 mosmol/kgH(2)O significantly stimulated (doubled) urea permeability; it returned to control levels on inhibition of PKC with either 10 μM chelerythrine or 50 μM rottlerin. To determine the potential synergy between vasopressin and PKC, phorbol dibutyrate (PDBu) was used to stimulate PKC. Vasopressin stimulated urea permeability 247%. Although PDBu alone did not change basal urea permeability, in the presence of vasopressin, it significantly increased urea permeability an additional 92%. The vasopressin and PDBu-stimulated urea permeability was reduced to AVP alone levels by inhibition of PKC. We conclude that hypertonicity stimulates urea transport through a PKC-mediated phosphorylation. Whether PKC directly phosphorylates UT-A1 and/or UT-A3 or phosphorylates it as a consequence of a cascade of activations remains to be determined.