The overall objective of the proposed research is to identify and characterize mechanisms responsible for intestinal transport of bile acids. To accomplish this objective, the first specific aim is to identify bile acid binding polypeptides in ileal basolateral membranes that are involved in bile acid transport using photoaffinity labeling. Studies are proposed to demonstrate that photolabile bile acid derivatives interact with and reversibly and irreversibly inhibit the recently described bile acid transport system in the basolateral membrane. Photoaffinity labeling of basolateral membranes with these derivatives then are performed to identify bile acid binding polypeptides using sodium dodecyl sulfate polyacrylamide gel electrophoresis. Binding polypeptides involved in bile acid transport in ileal basolateral membrane vesicles will be compared to those in jejunal plasma membranes, ileal brush border membranes and plasma membranes of hepatocytes. The second specific, yet inter-related, aim is to identify the intracellular pathway of bile acid transport. From a description of the kinetics and characteristics of bile acid uptake (or lack of uptake) by epithelial cell organelles a model of transcellular transport can be proposed. Photoaffinity labeling with bile acid photoprobes of intact enterocytes and subsequent cellular fractionation should identify subcellular sites of bile acid covalent binding. Pulse-chase experiments are desinged to follow the transepithelial route of bile acids with respect to time. The methods of procedure combine the sequential breakdown of the small intestine with covalent binding techniques to identify subcellular components that are intimately involved in bile acid transport. These experiments should provide not only greater understanding of the controlling mechanisms for bile acid intestinal transport but also insight into the basic but unresolved question of how transepithelial translocation occurs for all transport systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK032045-05
Application #
3230522
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1982-07-01
Project End
1988-12-31
Budget Start
1987-07-01
Budget End
1988-12-31
Support Year
5
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Pennsylvania State University
Department
Type
Schools of Medicine
DUNS #
129348186
City
Hershey
State
PA
Country
United States
Zip Code
17033
Gong, Y Z; Kato, T; Schwartz, D A et al. (1996) Ontogenic and glucocorticoid-accelerated expression of rat 14 kDa bile acid-binding protein. Anat Rec 245:532-8
Gong, Y Z; Everett, E T; Schwartz, D A et al. (1994) Molecular cloning, tissue distribution, and expression of a 14-kDa bile acid-binding protein from rat ileal cytosol. Proc Natl Acad Sci U S A 91:4741-5
Lin, M C; Weinberg, S L; Kramer, W et al. (1988) Identification and comparison of bile acid-binding polypeptides in ileal basolateral membrane. J Membr Biol 106:1-11