Awardee OrganizationBOSTON UNIVERSITY MEDICAL CAMPUS
Description
Abstract Text
Despite much study little is known about the basolateral
conductance in sodium transporting epithelia and of the factors
regulating it in response to alterations in the rate of sodium
transport. Although it is clearly established that most of the
basolateral conductance in frog skin, a widely used model for
sodium absorbing epithelia, is due to potassium, the nature of the
potassium and other ion channels and their possible modulation by
intracellular factors are unknown. Recent technical advances
have made it possible to record single ion channel currents
flowing through a small patch of cell membrane and to
characterize unambiguously the components of complex
macroscopic currents in isolated cells. Preliminary experiments
have shown the feasibility of applying these "patch-clamp"
techniques to enzymatically isolated viable epithelial cells from
the frog skin. Experiments are proposed in intact isolated
epithelia and dispersed cells to characterize the elementary
properties (i.e. single-channels conductance, voltage- and time-
dependent gating kinetics, ionic selectivity) of the ion channels
that constitute the conductance pathways of the basolateral
membrane. The effects on channel activity of possible
intracellular regulating agents (pH, free Ca and Na
concentrations, ATP) as well as the role of protein
phosphorylation (by cAMP-dependent protein kinase) will be
analyzed. Other experiments in intact epithelia treated with
ionophores will characterize the macroscopic K current so that it
will be possible to identify the channels responsible for the
basolateral membrane K conductance under different conditions.
Patch-clamp techniques will be used also to investigate the
response of basolateral channels in isolated cells and intact
epithelia to modifiers of Na transport (vasopressin, isoproterenol,
etc.). The results of these experiments will help elucidate the
mechanisms of ion transport and their regulation at the
basolateral membrane of Na absorbing epithelia and will lead to a
better understanding of the interactions between transepithelial
transport and cell homeostasis.
National Institute of Diabetes and Digestive and Kidney Diseases
CFDA Code
DUNS Number
604483045
UEI
FBYMGMHW4X95
Project Start Date
01-August-1988
Project End Date
31-July-1992
Budget Start Date
01-August-1990
Budget End Date
31-July-1992
Project Funding Information for 1990
Total Funding
$107,485
Direct Costs
$62,130
Indirect Costs
$45,355
Year
Funding IC
FY Total Cost by IC
1990
National Institute of Diabetes and Digestive and Kidney Diseases
$107,485
Year
Funding IC
FY Total Cost by IC
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