The overall goal of the Program Project is to characterize host- environment interactions within the intestinal tract. Within this central theme, the Program examines the hosts' response to a protein antigen that activates human celiac disease, to an enteric bacterial pathogen, S. dublin, and to the protozoan parasites G. lamblia and E. histolytica. Other aspects of the Program examine the influence of the intestinal environment on S. dublin, G. lamblia and E. histolytica, as well as interactions between key components of the mucosal immune system and those pathogens. The Program consists of six Projects and four Cores, and brings together investigators with substantial expertise in immunology, molecular biology, and microbiology from three Departments and four Divisions to accomplish the Program's major objectives. Research Unit 1, Project 1, will explore the immunogenetic basis of an intestinal disease (celiac disease) that is activated by exposure to common dietary proteins (i.e., wheat gliadins and similar proteins in other grains). Research Unit 1, Project 2, will study the molecular mechanisms by which specific cytokines regulate the late stages of IgA B cell differentiation, will investigate cytokine production by the intestinal epithelium as an early signaling system to the adjacent and underlying cells of the mucosal immune system, and will examine the role mucosal cytokines play in determining host susceptibility and resistance to the enteric pathogen S. dublin. Research Unit 2 will study the hosts' interaction with a protozoan parasite, Giardia lamblia, strategies that the parasite uses to survive in the host and to evade host defense mechanisms and that the host uses in its interaction with this parasite. Research Unit 3 examines virulence plasmid-encoded strategies employed by an enteric pathogen, S. dublin, to avoid both humoral and cellular host defenses and explores factors important for host resistance to Salmonella. Research Unit 4 will examine the molecules on intestinal epithelial cells that are important in the host interaction with gamma/delta T cells, examine the peptides recognized by gamma/delta T cells and in collaboration with Units 2 and 3, characterize the importance of gamma/delta T cells in host defense to bacterial and parasitic pathogens. Facilities in the areas of tissue culture, molecular biology, the development of transgenic lines of mice, murine breeding and maintenance, and administrative services offer quality services and tightly interlink the Projects. This Program has provided significant insights into mechanisms important in intestinal disease and should continue to provide new information and new strategies for the prevention and treatment of intestinal disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK035108-10
Application #
2139492
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1985-04-01
Project End
1998-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
10
Fiscal Year
1994
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
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Lakhdari, Omar; McAllister, Christopher S; Wang, Michael et al. (2016) TLR3 signaling is downregulated by a MAVS isoform in epithelial cells. Cell Immunol 310:205-210
de Jong, Petrus R; Taniguchi, Koji; Harris, Alexandra R et al. (2016) ERK5 signalling rescues intestinal epithelial turnover and tumour cell proliferation upon ERK1/2 abrogation. Nat Commun 7:11551
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de Jong, Petrus R; Takahashi, Naoki; Harris, Alexandra R et al. (2014) Ion channel TRPV1-dependent activation of PTP1B suppresses EGFR-associated intestinal tumorigenesis. J Clin Invest 124:3793-806

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