Na+/H+ exchangers (NHEs) mediate electroneutral, amiloride-sensitive exchange of Na+ and H+ across plasma membranes in most eukaryotic cells. In the mammalian kidney, this activity contributes to the maintenance of acid/base balance and NaCl homeostasis and has been described on both apical and/or basolateral surfaces of most segments of the nephron. Although the Na+/H+ exchanger located on the apical membrane (brush border) of the proximal tubule is sensitive to many factors including metabolic pH and hormones such as angiotensin II and parathyroid hormone the molecular mechanisms involved in regulation are not understood. This project will test the hypothesis that subcellular compartmentalization and molecular assembly represent critical aspects of the regulation of the renal brush border Na+/H+ exchange activity. Membrane fractionation studies in our laboratory have shown that the brush border Na+/H+ exchanger, NHE3, exists in both microvillar and non-microvillar membranes and that the relative level of the expression of NHE3 in these compartments shifts in relation to the acid/base status of the animal. Moreover, recent immunochemical studies have also shown that NHE3 exists in two distinct oligomeric states. One is a large (21S) complex with the brush border protein megalin and which is concentrated in dense, non-microvillar membranes, The other is a smaller (9.6S) form, not associated with megalin, and which is concentrated in the microvilli of the brush border. These data allow us to propose a model in which the Na+/H+ exchanger in regulated by mechanisms that include both the interaction with megalin and trafficking between distinct membrane compartments. Based upon these preliminary data we will describe at the molecular level the regulation of this important renal transport activity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK054933-01A2
Application #
6285013
Study Section
General Medicine B Study Section (GMB)
Program Officer
Scherbenske, M James
Project Start
2001-02-01
Project End
2005-01-31
Budget Start
2001-02-01
Budget End
2002-01-31
Support Year
1
Fiscal Year
2001
Total Cost
$281,600
Indirect Cost
Name
Yale University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Gotoh, Nanami; Yan, Qingshang; Du, Zhaopeng et al. (2010) Altered renal proximal tubular endocytosis and histology in mice lacking myosin-VI. Cytoskeleton (Hoboken) 67:178-92
Li, Yuanli; Cong, Rong; Biemesderfer, Daniel (2008) The COOH terminus of megalin regulates gene expression in opossum kidney proximal tubule cells. Am J Physiol Cell Physiol 295:C529-37
Biemesderfer, D (2006) Regulated intramembrane proteolysis of megalin: linking urinary protein and gene regulation in proximal tubule? Kidney Int 69:1717-21
McDonough, Alicia A; Biemesderfer, Daniel (2003) Does membrane trafficking play a role in regulating the sodium/hydrogen exchanger isoform 3 in the proximal tubule? Curr Opin Nephrol Hypertens 12:533-41
Biemesderfer, Daniel; Mentone, Sue Ann; Mooseker, Mark et al. (2002) Expression of myosin VI within the early endocytic pathway in adult and developing proximal tubules. Am J Physiol Renal Physiol 282:F785-94