The long term objective of this proposal is to characterize the ion transport systems in subpopulations of apical and basolateral membranes and of intravesicular organelles of renal cells. Another long term objective is to define the factors which regulate ion transport at the cell membrane level. The hypothesis that there is a dynamic relationship between ion transporters in the cell membrane and in intracellular vesicle populations will be examined.
The specific aims of the project are: 1. To identify and characterize the transport systems for Na+, H+, K+, C1-, and other anions in renal cell membranes. 2. To evaluate the effects of in vivo conditioning (diet, acidosis, hormones, etc.) on the activity of renal cell membrane transport systems. 3. To investigate the ion transport systems in continuous cell lines of renal origin. 4. To determine the role played by intracellular pools of transpoerrts in the regulation of renal cell membrane transport systems (""""""""membrane recycling hypothesis""""""""). 5. To evaluate the nature and regulatory role of secondary sites (""""""""modifier sites"""""""") on ion transport systems which may regulate transport activity by kinetic mechanisms. Cell membrane populations will be prepared by differential centrifugation, density gradient fractionation techniques, and counter-current distribution in aqueous 2-phase systems. Membrane populations will be identified by marker enzyme determinations and morphologic studies with an electron microscope. Ion transport studies will be done with standard isotopic techniques and fluorescence methods for measuring transmembrane pH and voltage gradients. Understanding the mechanisms of ion transport and factors which regulate these systems will be an important step in furthering the overall understanding of renal function, as well as defining the nature of adaptive changes to physiologic pertubations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK019407-11
Application #
3226362
Study Section
General Medicine B Study Section (GMB)
Project Start
1979-05-01
Project End
1989-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
11
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Warnock, D G (2001) Genetic forms of human hypertension. Curr Opin Nephrol Hypertens 10:493-9
Meneton, P G; Warnock, D (2001) Involvement of renal apical Na transport systems in the control of blood pressure. Am J Kidney Dis 37:S39-47
Oh, Y S; Lee, S; Won, C et al. (2001) An Alu cassette in the human epithelial sodium channel. Biochim Biophys Acta 1520:94-8
Saxena, S; Quick, M W; Warnock, D G (2000) Interaction of syntaxins with epithelial ion channels. Curr Opin Nephrol Hypertens 9:523-7
Oh, Y S; Warnock, D G (2000) Disorders of the epithelial Na(+) channel in Liddle's syndrome and autosomal recessive pseudohypoaldosteronism type 1. Exp Nephrol 8:320-5
Peti-Peterdi, J; Chambrey, R; Bebok, Z et al. (2000) Macula densa Na(+)/H(+) exchange activities mediated by apical NHE2 and basolateral NHE4 isoforms. Am J Physiol Renal Physiol 278:F452-63
Warnock, D G (2000) Aldosterone-related genetic effects in hypertension. Curr Hypertens Rep 2:295-301
Warnock, D G (2000) Low renin hypertension in the next millennium. Semin Nephrol 20:40-6
Karim, Z G; Chambrey, R; Chalumeau, C et al. (1999) Regulation by PKC isoforms of Na(+)/H(+) exchanger in luminal membrane vesicles isolated from cortical tubules. Am J Physiol 277:F773-8
Warnock, D G (1999) Hypertension. Semin Nephrol 19:374-80

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