The aim of this application is to identify the role(s) of adenosine and adenosine receptors in the regulation of ion transport in renal and intestinal epithelia. Specifically, we propose to localize A1 and A2 adenosine receptors to cells from isolated segments of the mammalian nephron (glomeruli and tubular segments) and ileum (crypt and villus cells) using receptor-ligand binding techniques. We will characterize separate transport pathways for adenosine across brush-border and basdolateral membranes of epithelial cells and measure adenosine concentrations in interstitial fluid. We will determine the mechanisms of receptor signal transduction in a model epithelium with functional A1 and A2 adenosine receptors. Methods include radioligandreceptor binding studies with high activity agonists and antagonists, measurements of adenylate cyclase activity, ADP ribosylation, polyacrylamide gel electrophoresis and autoradiography of GTP binding regulatory proteins, primary culture of rectal gland cells, studies of 3H- adenosine transport in isolated membrane vesicles, measurements of interstitial adenosine and intracellular calcium concentrations, and in vitro perfusion of shark rectal glands. The proposal will examine the hypothesis that external receptors for adenosine are present on enterocytes and renal tubular cells and are physiologic regulators of ion transport in these epithelia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK034208-06
Application #
3232547
Study Section
General Medicine B Study Section (GMB)
Project Start
1984-07-01
Project End
1992-06-30
Budget Start
1989-08-01
Budget End
1990-06-30
Support Year
6
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Forrest Jr, John N (2016) THE SHARK RECTAL GLAND MODEL: A CHAMPION OF RECEPTOR MEDIATED CHLORIDE SECRETION THROUGH CFTR. Trans Am Clin Climatol Assoc 127:162-175
Schwarz, Julia S; de Jonge, Hugo R; Forrest Jr, John N (2015) Value of Organoids from Comparative Epithelia Models. Yale J Biol Med 88:367-74
Stahl, Klaus; Stahl, Maximilian; de Jonge, Hugo R et al. (2015) ANP and CNP activate CFTR expressed in Xenopus laevis oocytes by direct activation of PKA. J Recept Signal Transduct Res 35:493-504
De Jonge, Hugo R; Tilly, Ben C; Hogema, Boris M et al. (2014) cGMP inhibition of type 3 phosphodiesterase is the major mechanism by which C-type natriuretic peptide activates CFTR in the shark rectal gland. Am J Physiol Cell Physiol 306:C343-53
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Stahl, Maximilian; Stahl, Klaus; Brubacher, Marie B et al. (2012) Divergent CFTR orthologs respond differently to the channel inhibitors CFTRinh-172, glibenclamide, and GlyH-101. Am J Physiol Cell Physiol 302:C67-76
Ratner, Martha A; Decker, Sarah E; Aller, Stephen G et al. (2006) Mercury toxicity in the shark (Squalus acanthias) rectal gland: apical CFTR chloride channels are inhibited by mercuric chloride. J Exp Zool A Comp Exp Biol 305:259-67
Bewley, Marie S; Pena, John T G; Plesch, Florian N et al. (2006) Shark rectal gland vasoactive intestinal peptide receptor: cloning, functional expression, and regulation of CFTR chloride channels. Am J Physiol Regul Integr Comp Physiol 291:R1157-64
Weber, Gerhard J; Mehr, Ali Poyan; Sirota, Jeffrey C et al. (2006) Mercury and zinc differentially inhibit shark and human CFTR orthologues: involvement of shark cysteine 102. Am J Physiol Cell Physiol 290:C793-801

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