The goal of this project is to obtain a molecular understanding of solute and water transport across the intestinal epithelium, and to elucidate how these processes are controlled by hormones and toxins. Membrane vesicles isolated from the brush border and basolateral surfaces of epithelial cells will be used to study the mechanisms of solute transport. Transport across the plasma membranes of vesicles will be measured using radioactive tracers and optical probes. Tracers will yield information about diffusive and carrier mediated transport, while optical probes will be used to obtain membrane potentials, ion permeability ratios, and net fluxes. These methods will be used to examine in detail ion conductive pathways (channels), KC1 symport, and C1/OH antiport in basolateral membranes, and Na-cotransport systems (Na-lactate) in brush border membranes. In the long term we propose to study these processes by electrophysiological techniques in planar bilayers (""""""""patch-clamp"""""""" preparations). Regulation of ion transport systems in plasma membranes by hormones (e.g., VIP) will also be explored by these techniques, and interactions between hormones, receptors and cyclases will be evaluated by radiation inactivation analysis. This project should provide a clear understanding of ion and solute transport across the epithelial cells of the small intestine in health and disease. In particular, our studies will provide insight into the molecular mechanisms of secretory diarrhea caused by hormones (e.g., VIP) and toxins (e.g., cholera toxin).

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK019567-12
Application #
3226439
Study Section
(SSS)
Project Start
1976-12-01
Project End
1988-11-30
Budget Start
1987-12-01
Budget End
1988-11-30
Support Year
12
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Kepe, Vladimir; Scafoglio, Claudio; Liu, Jie et al. (2018) Positron emission tomography of sodium glucose cotransport activity in high grade astrocytomas. J Neurooncol 138:557-569
Paz, Aviv; Claxton, Derek P; Kumar, Jay Prakash et al. (2018) Conformational transitions of the sodium-dependent sugar transporter, vSGLT. Proc Natl Acad Sci U S A 115:E2742-E2751
Gorraitz, Edurne; Hirayama, Bruce A; Paz, Aviv et al. (2017) Active site voltage clamp fluorometry of the sodium glucose cotransporter hSGLT1. Proc Natl Acad Sci U S A 114:E9980-E9988
Ghezzi, Chiara; Yu, Amy S; Hirayama, Bruce A et al. (2017) Dapagliflozin Binds Specifically to Sodium-Glucose Cotransporter 2 in the Proximal Renal Tubule. J Am Soc Nephrol 28:802-810
Sala-Rabanal, Monica; Hirayama, Bruce A; Ghezzi, Chiara et al. (2016) Revisiting the physiological roles of SGLTs and GLUTs using positron emission tomography in mice. J Physiol 594:4425-38
Zeuthen, Thomas; Gorraitz, Edurne; Her, Ka et al. (2016) Structural and functional significance of water permeation through cotransporters. Proc Natl Acad Sci U S A 113:E6887-E6894
Adelman, Joshua L; Ghezzi, Chiara; Bisignano, Paola et al. (2016) Stochastic steps in secondary active sugar transport. Proc Natl Acad Sci U S A 113:E3960-6
Gallo, Linda A; Wright, Ernest M; Vallon, Volker (2015) Probing SGLT2 as a therapeutic target for diabetes: basic physiology and consequences. Diab Vasc Dis Res 12:78-89
Scafoglio, Claudio; Hirayama, Bruce A; Kepe, Vladimir et al. (2015) Functional expression of sodium-glucose transporters in cancer. Proc Natl Acad Sci U S A 112:E4111-9
Adelman, Joshua L; Sheng, Ying; Choe, Seungho et al. (2014) Structural determinants of water permeation through the sodium-galactose transporter vSGLT. Biophys J 106:1280-9

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