Crohn's disease (CD) is a debilitating chronic condition with no known cure. Although there is evidence for the involvement of genetic, immunological, and environmental mechanisms, the precise cause(s) of CD remain unclear. Indirect evidence suggest that CD may be initiated by a dysregulated innate immune response against an """"""""unknown"""""""" antigen in a genetically susceptible host. The major strengths of this competitive renewal are the unique SAMP1/YitFc (SAMP) mouse model, which has been extensively characterized by our group during the last funding period, and the highly synergistic nature of the program. The overall objective of this continuation proposal is to investigate the key pathogenic mechanisms underlying this spontaneous murine model of CD. The Program Project will continue to be directed by Dr. Fabio Cominell, and will consist of 5 projects and 2 cores. Project 1, headed by Dr. Cominelli, will extend its focus on the role of pivotal cytokines in mediating chronic intestinal inflammation in this model. Project 2, headed by Dr. Marcia McDuffie, will identify susceptibility genes involved in the predisposition to ileitis in SAMP mice based on the chromosomal loci identified during the previous funding period. Project 3, headed by Dr. Steven Cohn, will investigate the role of Paneth cells and their defensins in initiating ileitis. Project 4, headed by Dr. Klaus Ley, will study the mechanisms of lymphocyte homing and trafficking in SAMP mice, with a particular focus on L-selectin and PSGL-1. Project 5, a new project headed by Dr. Theresa Pizarro, will investigate the role of epithelial innate immune responses in initiating and perpetuating ileitis in SAMP mice. This Program is supported by an Administrative Core, which coordinates the program, and an Animal Core, which centralizes the production and breeding of SAMP mice and other congenic lines. The long-term goal of this Program Project is to understand the key pathogenic mechanisms of experimental CD, to aid development of a cure for at least a subgroup of patients with this devastating disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
3P01DK057880-07S1
Application #
7364042
Study Section
Special Emphasis Panel (ZDK1-GRB-2 (M3))
Program Officer
Hamilton, Frank A
Project Start
2007-01-01
Project End
2010-08-31
Budget Start
2007-03-15
Budget End
2007-08-31
Support Year
7
Fiscal Year
2007
Total Cost
$34,837
Indirect Cost
Name
University of Virginia
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Ernst, P B; Erickson, L D; Loo, W M et al. (2012) Spontaneous autoimmune gastritis and hypochlorhydria are manifest in the ileitis-prone SAMP1/YitFcs mice. Am J Physiol Gastrointest Liver Physiol 302:G105-15
Lou, Yuefen; Lu, Xiaojiong; Dang, Xitong (2012) FOXO1 Up-Regulates Human L-selectin Expression Through Binding to a Consensus FOXO1 Motif. Gene Regul Syst Bio 6:139-49
Reuter, Brian K; Pastorelli, Luca; Brogi, Marco et al. (2011) Spontaneous, immune-mediated gastric inflammation in SAMP1/YitFc mice, a model of Crohn's-like gastritis. Gastroenterology 141:1709-19
Pizarro, Theresa T; Pastorelli, Luca; Bamias, Giorgos et al. (2011) SAMP1/YitFc mouse strain: a spontaneous model of Crohn's disease-like ileitis. Inflamm Bowel Dis 17:2566-84
Gorfu, Gezahegn; Rivera-Nieves, Jesus; Hoang, Sharon et al. (2010) Beta7 integrin deficiency suppresses B cell homing and attenuates chronic ileitis in SAMP1/YitFc mice. J Immunol 185:5561-8
Shanahan, Michael T; Vidrich, Alda; Shirafuji, Yoshinori et al. (2010) Elevated expression of Paneth cell CRS4C in ileitis-prone SAMP1/YitFc mice: regional distribution, subcellular localization, and mechanism of action. J Biol Chem 285:7493-504
Pastorelli, Luca; Garg, Rekha R; Hoang, Sharon B et al. (2010) Epithelial-derived IL-33 and its receptor ST2 are dysregulated in ulcerative colitis and in experimental Th1/Th2 driven enteritis. Proc Natl Acad Sci U S A 107:8017-22
Gorfu, G; Rivera-Nieves, J; Ley, K (2009) Role of beta7 integrins in intestinal lymphocyte homing and retention. Curr Mol Med 9:836-50
Vidrich, Alda; Buzan, Jenny M; Brodrick, Brooks et al. (2009) Fibroblast growth factor receptor-3 regulates Paneth cell lineage allocation and accrual of epithelial stem cells during murine intestinal development. Am J Physiol Gastrointest Liver Physiol 297:G168-78
Reuter, Brian K; Pizarro, Theresa T (2009) Mechanisms of tight junction dysregulation in the SAMP1/YitFc model of Crohn's disease-like ileitis. Ann N Y Acad Sci 1165:301-7

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