The long-term goal of this 5-year Competing Continuation Grant Application is to understand the functional regulation of the renal-specific Na+-coupled Cl- cotransporters at a molecular level. The major focus of this application is to determine the molecular mechanisms of regulation of the Na-K-2Cl cotransporter by cyclic AMP [cAMP]. Increasing net NaCl reabsorption in the thick ascending limb of Henle [TAL] by hormones generating cAMP via their respective Gs-coupled receptors is a fundamental mechanism for regulating salt transport in this nephron segment. The effects of these hormones is crucial to the normal functioning of the TAL in reabsorbing 10-15% of filtered NaCl, providing for normal diluting and concentrating power, and regulating divalent mineral excretion. Two major splice variants of the renal-specific Na-K-2CI cotransporter have been recently identified by us and both are expressed in the TAL. The novel hypothesis to be examined in this grant application is that the unique splice variant of the murine Na-K-2CI cotransporter, mBSC1-4, provides the fundamental mechanism for regulating Na-K-2CI cotransporter, mBSC1-9, activity by cAMP-dependent phosphorylation processes. Our working hypothesis is that mBSC1-4 exerts a dominant-negative like effect on mBSC1-9 cotransporter function that is modulated by cAMP-dependent phosphorylation processes. mBSC1-4 is also expressed in the ascending thin limb (aTL) and may serve important transport functions in this nephron segment that is importantly involved in urine dilution and concentration. Using a combination of molecular, biochemical, and physiological approaches, we will: a), characterize the mBSC1-9:mBSC1-4 interactions and the mechanism of cAMP-dependent regulation of Na+ transport [the TAL model]; b) assess mBSC1-4 and mBSCl-9 phosphorylation in the regulation of Na-K-2CI cotransport and mBSC1-4:mBSCl-9 interactions; c), characterize the function and regulation of mBSC1-4 independent of mBSC1-9 [the aTL model]; d), examine the effects of altering water balance or NaCl balance, K+ loading, and alterations in acid-base balance in the regulation of mBSCI-9 and mBSCI-4 in vivo. Results of these studies should begin to define the molecular mechanisms of regulating ion transport by phosphorylation processes in the ascending limb of Henle. This has important relevance to understanding salt and water handling by the kidney in health and disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK036803-14A1
Application #
6044853
Study Section
General Medicine B Study Section (GMB)
Program Officer
Scherbenske, M James
Project Start
1985-07-01
Project End
2005-07-31
Budget Start
2000-08-15
Budget End
2001-07-31
Support Year
14
Fiscal Year
2000
Total Cost
$288,263
Indirect Cost
Name
Yale University
Department
Physiology
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Garzon-Muvdi, Tomas; Pacheco-Alvarez, Diana; Gagnon, Kenneth B E et al. (2007) WNK4 kinase is a negative regulator of K+-Cl- cotransporters. Am J Physiol Renal Physiol 292:F1197-207
de Los Heros, Paola; Kahle, Kristopher T; Rinehart, Jesse et al. (2006) WNK3 bypasses the tonicity requirement for K-Cl cotransporter activation via a phosphatase-dependent pathway. Proc Natl Acad Sci U S A 103:1976-81
Paredes, Anahi; Plata, Consuelo; Rivera, Manuel et al. (2006) Activity of the renal Na+-K+-2Cl- cotransporter is reduced by mutagenesis of N-glycosylation sites: role for protein surface charge in Cl- transport. Am J Physiol Renal Physiol 290:F1094-102
Gamba, Gerardo (2005) Role of WNK kinases in regulating tubular salt and potassium transport and in the development of hypertension. Am J Physiol Renal Physiol 288:F245-52
Rinehart, Jesse; Kahle, Kristopher T; de Los Heros, Paola et al. (2005) WNK3 kinase is a positive regulator of NKCC2 and NCC, renal cation-Cl- cotransporters required for normal blood pressure homeostasis. Proc Natl Acad Sci U S A 102:16777-82
Mercado, Adriana; Mount, David B; Gamba, Gerardo (2004) Electroneutral cation-chloride cotransporters in the central nervous system. Neurochem Res 29:17-25
Hebert, Steven C; Mount, David B; Gamba, Gerardo (2004) Molecular physiology of cation-coupled Cl- cotransport: the SLC12 family. Pflugers Arch 447:580-93
Gamba, Gerardo; Bobadilla, Norma A (2004) Molecular physiology of the renal Na(+)-Cl- and Na(+)-K(+)-2Cl- cotransporters. Adv Exp Med Biol 559:55-65
Wilson, Frederick H; Kahle, Kristopher T; Sabath, Ernesto et al. (2003) Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4. Proc Natl Acad Sci U S A 100:680-4
Meade, Patricia; Hoover, Robert S; Plata, Consuelo et al. (2003) cAMP-dependent activation of the renal-specific Na+-K+-2Cl- cotransporter is mediated by regulation of cotransporter trafficking. Am J Physiol Renal Physiol 284:F1145-54

Showing the most recent 10 out of 34 publications