Awardee OrganizationWEILL MEDICAL COLL OF CORNELL UNIV
Description
Abstract Text
The cortical collecting tubule (CCT) of the mammalian kidney is
responsible for the final regulation of urine pH and potassium (K)
concentration. The 2 major cell types involved in this regulation are
the Na-transporting principal cells and the acid-base regulating
intercalated cells. recent evidence suggests the presence of a gastric-
type acid transporter (H-K ATPase) in the renal collecting duct. This
proposal focuses on the contribution of a functionally identified H-K
exchanger (H-K ATPase) to the process of acid-base and K homeostasis in
intercalated cells of the cortical collecting tubule, utilizing
fluorescence measurements of intracellular pH and calcium.
Six specific aims will be addressed using three related preparations.
The functional activity of the H-K exchanger will be monitored by
measuring the rate of K-dependent intracellular pH recovery in response
to an imposed acid load. the role of this exchanger in K reabsorption
and H secretion and regulation by pH, K and aldosterone will be examined.
Basic characterization of the H-K exchanger includes assessing the
functional similarity of the exchanger to the well-characterized gastric
H-K ATPase, apical/basolateral localization of the exchanger, and
defining its contribution to intracellular pH regulation under basal
conditions. Preparations appropriate to selected aims include: split
open cortical collecting tubules, isolated parietal cells, and isolated
perfused cortical collecting tubules, loaded with the intracellular pH
indicator, BCECF or the intracellular Ca indicator, Fura-2. In addition,
the unesterified forms of BCECF and PBFI, a K-specific indicator, will
be used for perfused tubule studies.
Functional characterization of an H-K exchange mechanism and localization
of this mechanism may help explain a number of clinical observations:
1. the association between low serum K and extracellular alkalosis, 2.
the relationship between metabolic acidosis and reduced excretion of K
which can elevate serum K to a point where it interferes with electrical
activity of the heart. The results of these studies will provide
important information on normal and pathological K states and will
influence our understanding of K balance during metabolic abnormalities
and diuretic therapy.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
acid base balanceadenosinetriphosphatasealdosteroneapical membranebasolateral membraneelectrolyte balancehydrogen transportintracellular transportlaboratory rabbitlaboratory ratmembrane transport proteinsperfusionpotassiumrenal tubular transport
National Institute of Diabetes and Digestive and Kidney Diseases
CFDA Code
DUNS Number
060217502
UEI
YNT8TCJH8FQ8
Project Start Date
01-August-1993
Project End Date
31-July-1998
Budget Start Date
01-August-1995
Budget End Date
31-July-1996
Project Funding Information for 1995
Total Funding
$120,677
Direct Costs
$70,104
Indirect Costs
$50,573
Year
Funding IC
FY Total Cost by IC
1995
National Institute of Diabetes and Digestive and Kidney Diseases
$120,677
Year
Funding IC
FY Total Cost by IC
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