The long-term goal of the investigations described in this proposal is to define the precise intracellular mechanisms responsible for the control of active transcellular transport of chloride ions by the intestinal epithelium. This transport is the major driving force for th movement of water into the intestinal lumen and, accordingly, its over- expression is the primary basis for secretory diarrhea. Studies accomplished during the current funding period have identified both positive and negative intracellular signals, or messengers, that regulat the overall level of chloride secretion in response to hormones that increase intracellular levels of cytoplasmic calcium. It is now propose to examine the exact nature of these signals, how they are generated within the cell, and the mechanisms whereby they exert their positive or negative effects. Two specific hypotheses will be tested. First, that inositol (3,4,5,6) tetrakisphosphate (InsP4) is a negative signal that is mobilized by calcium-mobilizing agonists such as carbachol, via the tyrosine phosphorylation of phospholipase C-gamma, and that this molecul may interact with basolateral potassium channels and/or apical chloride channels to limit secretion. Second, that cyclic AMP (camp) can potentiate the secretory effects of carbachol by modifying the productio of putative negative signals, such as the influx of calcium from the extracellular environment and/or the synthesis of InsP4. The general strategy that will be employed to address these hypotheses will be to correlate biochemical and physiological parameters in a well- characterized cell culture model of the intestinal epithelium, the T84 cell line. Techniques to be employed include Ussing chamber, isotope flux and patch clamp studies of ion transport, biochemical analyses of inositol phosphates and tyrosine phosphorylation, and fluorescence imaging of intracellular calcium concentrations. The significance of th studies lies in their potential to increase our understanding of the cellular abnormalities underlying secretory diarrhea. Ultimately, improved knowledge of such abnormalities might be expected to suggest better therapeutic approaches to this condition.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK028305-16
Application #
2608379
Study Section
General Medicine A Subcommittee 2 (GMA)
Program Officer
May, Michael K
Project Start
1981-07-01
Project End
1998-11-30
Budget Start
1997-12-01
Budget End
1998-11-30
Support Year
16
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Barrett, Kim E; McCole, Declan F (2016) Hydrogen peroxide scavenger, catalase, alleviates ion transport dysfunction in murine colitis. Clin Exp Pharmacol Physiol 43:1097-1106
Hoda, M Raschid; Scharl, Michael; Keely, Stephen J et al. (2010) Apical leptin induces chloride secretion by intestinal epithelial cells and in a rat model of acute chemotherapy-induced colitis. Am J Physiol Gastrointest Liver Physiol 298:G714-21
McCole, D F; Barrett, K E (2009) Decoding epithelial signals: critical role for the epidermal growth factor receptor in controlling intestinal transport function. Acta Physiol (Oxf) 195:149-59
Scharl, Michael; Paul, Gisela; Weber, Achim et al. (2009) Protection of epithelial barrier function by the Crohn's disease associated gene protein tyrosine phosphatase n2. Gastroenterology 137:2030-2040.e5
Chappell, Alfred E; Bunz, Michael; Smoll, Eric et al. (2008) Hydrogen peroxide inhibits Ca2+-dependent chloride secretion across colonic epithelial cells via distinct kinase signaling pathways and ion transport proteins. FASEB J 22:2023-36
Tillinger, Wolfgang; McCole, Declan F; Keely, Stephen J et al. (2008) Hypertonic saline reduces neutrophil-epithelial interactions in vitro and gut tissue damage in a mouse model of colitis. Am J Physiol Regul Integr Comp Physiol 295:R1839-45
McCole, Declan F; Barrett, Kim E (2007) Varied role of the gut epithelium in mucosal homeostasis. Curr Opin Gastroenterol 23:647-54
McCole, Declan F; Truong, Anh; Bunz, Michael et al. (2007) Consequences of direct versus indirect activation of epidermal growth factor receptor in intestinal epithelial cells are dictated by protein-tyrosine phosphatase 1B. J Biol Chem 282:13303-15
Keely, Stephen J; Scharl, Michael M; Bertelsen, Lone S et al. (2007) Bile acid-induced secretion in polarized monolayers of T84 colonic epithelial cells: Structure-activity relationships. Am J Physiol Gastrointest Liver Physiol 292:G290-7
Chow, Jimmy Y C; Barrett, Kim E (2007) Role of protein phosphatase 2A in calcium-dependent chloride secretion by human colonic epithelial cells. Am J Physiol Cell Physiol 292:C452-9

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