The current submission of the Program Project Grant (PPG), Cellular Decisions of Differentiation in the Gl Tract integrates the efforts of three investigators (two basic science and one clinical) from three Departments at the University of Michigan. The central goals of the proposed studies generally remain the same as the prior two cycles: (a) To understand how gastric epithelial cells develop and maintain their identity by expressing or responding to developmental signaling pathways activated by the peptide morphogen sonic hedgehog (Shh) or the transmembrane signaling receptor Notch (b) To investigate how the patterns of cellular differentiation in the gastric corpus, gastric antrum and intestine use these signaling pathways to maintain homeostasis or respond to environmental stress, e.g., chronic inflammation. Subproject #1 entitled Modulation of myeloid cell phenotype by hedgehog signals will expand upon the intial translational observation that the Hedgehog target gene Glil expressed in myeloid cells modulates the epithelial response to inflammation. Subproject #2 entitled Role of Hedgehog signaling in chronic gastritis and metaplasia will examine the role of chronic inflammation, specifically proinflammatory cytokines in mediating changes in patterns of cellular differentiation, e.g., metaplasia in the gastric corpus and hyperplasia in the antrum. Subproject #3 entitled Notch Regulation of Gastric Epithelial Cell Homeostasis and Tumorigenesis will explore the effect of the Notch pathway on Lgr5+ stem cells in the antrum and its possible interaction with the Hedgehog pathway. The PPG will support one service core (Cell Biology Core) to efficiently, process, analyze and coordinate tissue samples and flow cytometric analysis between the three projects. In summary, the PPG will use a variety of different mouse models and cell or molecular -based approaches to understand how gastric and intestinal cells maintain their homeostasis, but then modify their cellular patterns of differentiation in response to chronic inflammation ultimately directing the cll towards a pro-proliferative phenotype.

Public Health Relevance

The PPG brings together both basic and translational concepts to dissect the use developmental pathways, e.g.. Hedgehog and Notch signaling to execute cellular decisions for homeostasis versus pathologic responses to environmental stressors, e.g., bacterial infection, inflammation, chemical injury, which can segue to neoplastic transformation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK062041-15
Application #
9330842
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Greenwel, Patricia
Project Start
2002-09-15
Project End
2018-07-31
Budget Start
2017-08-01
Budget End
2018-07-31
Support Year
15
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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Merchant, Juanita L (2018) Parietal Cell Death by Cytokines. Cell Mol Gastroenterol Hepatol 5:636-637
El-Zaatari, Mohamad; Bass, Adam J; Bowlby, Reanne et al. (2018) Indoleamine 2,3-Dioxygenase 1, Increased in Human Gastric Pre-Neoplasia, Promotes Inflammation and Metaplasia in Mice and Is Associated With Type II Hypersensitivity/Autoimmunity. Gastroenterology 154:140-153.e17
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Gifford, Gail B; Demitrack, Elise S; Keeley, Theresa M et al. (2017) Notch1 and Notch2 receptors regulate mouse and human gastric antral epithelial cell homoeostasis. Gut 66:1001-1011
Merchant, Juanita L; Ding, Lin (2017) Hedgehog Signaling Links Chronic Inflammation to Gastric Cancer Precursor Lesions. Cell Mol Gastroenterol Hepatol 3:201-210
Al Menhali, Asma; Keeley, Theresa M; Demitrack, Elise S et al. (2017) Gastrin induces parathyroid hormone-like hormone expression in gastric parietal cells. Am J Physiol Gastrointest Liver Physiol 312:G649-G657

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