This research is directed at an understanding of the mechanisms of H+ and Cl- transport by gastric mucosa. In recent years there has been great interest in the importance of the gastric (H++K+) ATPase as the primary gastric H+ pump, and the rather profound changes in membrane structure and transport function as the gastric oxyntic cells are stimulated to secrete hydrochloric acid. Normal physiological function of these cellular processes are essential for a healthy for a healthy stomach and effective digestion. The proposed research is developed within three major sections, based on the theme of principal questions being addressed. The first section examines the cell biology of the oxyntic cell in terms of the nature and regulation of membrane changes associated with HCl secretion. This will include an assessment of the morphological and functional changes in secretory membranes through all stages of physiological activity. The membranes will be isolated and characterized according to composition and transport activity. The mechanisms of cell and membrane activation will be studied through an examination of regulatory steps, such as membrane phosphorylation, as well as the role of cytoskeletal elements in regulating oxyntic cell form and menbrane transformations. The second section deals with a detailed analysis of the transport properties of isolated gastric membrane vesicles that are rich in (H++K+) ATPase. The major objectives here are to assess the mechanisms by which K+ and Cl- are transported when the membranes are """"""""activated"""""""" in the normal course of gastric stimulation. This research will also define the ways in which the systems of activated K+ and Cl- transport interdigitate with the H+/K+ exchange pump enzyme. The third section concentrates on the (H++K+) ATPase. These experiments will study detailed kinetics of the gastric pump enzyme. They are designed to elucidate the catalytic cycle of the enzyme and the nature of the principal energy translocation step in the cycle.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM010141-21
Application #
3150769
Study Section
Physiology Study Section (PHY)
Project Start
1974-09-01
Project End
1989-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
21
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Schwarzer, Christian; Fu, Zhu; Morita, Takeshi et al. (2015) Paraoxonase 2 serves a proapopotic function in mouse and human cells in response to the Pseudomonas aeruginosa quorum-sensing molecule N-(3-Oxododecanoyl)-homoserine lactone. J Biol Chem 290:7247-58
Natarajan, Paramasivam; Crothers Jr, James M; Rosen, Jared E et al. (2014) Myosin IIB and F-actin control apical vacuolar morphology and histamine-induced trafficking of H-K-ATPase-containing tubulovesicles in gastric parietal cells. Am J Physiol Gastrointest Liver Physiol 306:G699-710
Nakada, Stephanie L; Crothers Jr, James M; Machen, Terry E et al. (2012) Apical vacuole formation by gastric parietal cells in primary culture: effect of low extracellular Ca2+. Am J Physiol Cell Physiol 303:C1301-11
Zhu, Lixin; Crothers Jr, James; Zhou, Rihong et al. (2010) A possible mechanism for ezrin to establish epithelial cell polarity. Am J Physiol Cell Physiol 299:C431-43
Reenstra, W W; Bettencourt, J D; Forte, J G (1988) Kinetic studies of the gastric H,K-ATPase. Evidence for simultaneous binding of ATP and inorganic phosphate. J Biol Chem 263:19618-25
Urushidani, T; Forte, J G (1987) Stimulation-associated redistribution of H+-K+-ATPase activity in isolated gastric glands. Am J Physiol 252:G458-65
Urushidani, T; Hanzel, D K; Forte, J G (1987) Protein phosphorylation associated with stimulation of rabbit gastric glands. Biochim Biophys Acta 930:209-19
Reenstra, W W; Bettencourt, J D; Forte, J G (1987) Mechanisms of active Cl- secretion by frog gastric mucosa. Am J Physiol 252:G543-7
Reenstra, W W; Bettencourt, J D; Forte, J G (1986) Active K+ absorption by the gastric mucosa: inhibition by omeprazole. Am J Physiol 250:G455-60
Reenstra, W W; Forte, J G (1986) Mechanism of inhibition of gastric acid secretion by SCN-: interrelation of SCN- flux and inhibition. Am J Physiol 250:G76-84

Showing the most recent 10 out of 14 publications