Guanylin and uroguanylin are peptides that are expressed at mucosal surfaces and bind to the transmembrane receptor guanylate cyclase C (GC-C). Ligand binding to GC-C, also expressed on mucosal epithelial cells, elevates intracellular cGMP and elicits transmembrane ion movement via the cystic fibrosis transmembrane conductance regulator and the Na+/H+ Exchanger 3. This signaling pathway has direct clinical relevance in that acute illness caused by enterotoxigenic strains of E. coli is often mediated by the heat stable toxin STa, a super-agonist of GC-C. Using gene deleted mice as our model system, our preliminary data indicate that signaling through GC-C has an important role in regulating mucosal immune homeostasis. We further show that cGMP levels in the epithelial of the intestine are required for regulated, well-controlled NF-?B and that deletion of GC-C, and a subsequent drop in cGMP levels, results in a highly sensitized mucosal surface. Proinflammatory gene expression is elevated in mice with diminished mucosal cGMP levels and this is further exacerbated during lipopolysaccharide challenge. Further, we demonstrate that signaling through GC-C is important in host defense during infection by gastrointestinal pathogens such as Citrobacter rodentium. The overarching hypothesis of this application is that GC-C, via ligand-induced cGMP generation, is an essential regulator of epithelial NF-?B activity and that loss of this aspect of GC-C function deregulate mucosal innate immune homeostasis. We will address this in the following aims.
Specific Aim 1 will determine the role of GC- C signaling in NF-?B signal transduction and gene expression.
Specific Aim 2 will define the role of GC-C in bacterial pathogen infection. The studies in this proposal will define a novel and important link between GC-C regulated cGMP production and maintenance of mucosal immune homeostasis.

Public Health Relevance

Bacterial infection is an important source of morbidity and mortality in the United States and developing world. We have identified a novel connection between an intestinal protein called Guanylate Cyclase C (GC-C), the NF-?B signaling system, and resistance of the intestine to infection. This proposal will investigate ways in which GC-C blocks pathogen infection in the intestine and whether this process can be used to suppress gastrointestinal disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI107274-01
Application #
8568294
Study Section
Immunity and Host Defense Study Section (IHD)
Program Officer
Rothermel, Annette L
Project Start
2013-08-08
Project End
2015-07-31
Budget Start
2013-08-08
Budget End
2014-07-31
Support Year
1
Fiscal Year
2013
Total Cost
$179,775
Indirect Cost
$62,275
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
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Harmel-Laws, Eleana; Mann, Elizabeth A; Cohen, Mitchell B et al. (2013) Guanylate cyclase C deficiency causes severe inflammation in a murine model of spontaneous colitis. PLoS One 8:e79180
Mann, Elizabeth A; Harmel-Laws, Eleana; Cohen, Mitchell B et al. (2013) Guanylate cyclase C limits systemic dissemination of a murine enteric pathogen. BMC Gastroenterol 13:135