The long-term objective of this program is to provide new, useful information on the mechanisms by which gastrointestinal hormones (GIH) and related compounds influence body function. We plan to study the synthesis, storage, release, transport, and mechanisms of action of these agents on target cells, target-cell responses, the hormone-hormone interrelationships of these peptides, and their gene expression. In Project 1, we will examine the mechanisms underlying age-related changes in GI hormone metabolism and in responses of the gut and pancreas to trophic stimuli. We will determine the mechanisms by in which age-related changes in GI function may relate to development of disease. In Project 2, we will examine the relevance of chromogranin and its physiologic role in the GI tract and pancreas. We will investigate the action of pancreastatin on the release of insulin from the pancreas. In Project 3, we will examine the effects of GIH hormones on growth of cancers. We will study the mechanisms of trophic actions of GIH. We will determine the role of growth factors in control of growth of GI and pancreatic cancers. In Project 4, we will explore expression of mRNA for parathyroid hormone-related protein and calcitonin gene-related peptide by gut tissues and cells. We will determine the location of the peptides in the gut, identify cellular sites of synthesis and examine the regulation of mRNA expression by the cells. In Project 5, we will define cellular and intracellular mechanisms that mediate effects of steroids on functions of gut and pancreas and on the growth of colonic and pancreatic cancer cells. We will characterize estradiol-binding proteins from various gut and pancreatic tissues. We have established a new Molecular Pathobiology Core to study the effects of trophic gut peptides on expression of cell cycle-related genes and on the expression of autocrine growth factors. Histological localization of neuropeptide gene expression and regulatory mechanisms that affect the level of expression will be examined. Since the last competitive review, we have demonstrated by our publications that our collaboration has been productive; many publications relate to more than one project. With the support of this grant, we have continued to further expand the depth and breadth of our research to meet the long-term objective of this program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK035608-10
Application #
2139609
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1985-09-16
Project End
1996-03-31
Budget Start
1995-04-01
Budget End
1996-03-31
Support Year
10
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Surgery
Type
Schools of Medicine
DUNS #
041367053
City
Galveston
State
TX
Country
United States
Zip Code
77555
Bhatia, Vandanajay; Cao, Yanna; Ko, Tien C et al. (2016) Parathyroid Hormone-Related Protein Interacts With the Transforming Growth Factor-?/Bone Morphogenetic Protein-2/Gremlin Signaling Pathway to Regulate Proinflammatory and Profibrotic Mediators in Pancreatic Acinar and Stellate Cells. Pancreas 45:659-70
Staloch, Dustin; Gao, Xuxia; Liu, Ka et al. (2015) Gremlin is a key pro-fibrogenic factor in chronic pancreatitis. J Mol Med (Berl) 93:1085-1093
Mrazek, Amy A; Porro, Laura J; Bhatia, Vandanajay et al. (2015) Apigenin inhibits pancreatic stellate cell activity in pancreatitis. J Surg Res 196:8-16
Gao, Xuxia; Cao, Yanna; Staloch, Dustin A et al. (2014) Bone morphogenetic protein signaling protects against cerulein-induced pancreatic fibrosis. PLoS One 9:e89114
Bhatia, Vandanajay; Rastellini, Cristiana; Han, Song et al. (2014) Acinar cell-specific knockout of the PTHrP gene decreases the proinflammatory and profibrotic responses in pancreatitis. Am J Physiol Gastrointest Liver Physiol 307:G533-49
Gao, Xuxia; Cao, Yanna; Yang, Wenli et al. (2013) BMP2 inhibits TGF-?-induced pancreatic stellate cell activation and extracellular matrix formation. Am J Physiol Gastrointest Liver Physiol 304:G804-13
Deng, Xiyun; Cao, Yanna; Liu, Yan et al. (2013) Overexpression of Evi-1 oncoprotein represses TGF-? signaling in colorectal cancer. Mol Carcinog 52:255-264
Cao, Yanna; Zhang, Weili; Gao, Xuxia et al. (2013) PTHrP is a novel mediator for TGF-?-induced apoptosis. Regul Pept 184:40-6
Cao, Yanna; Yang, Wenli; Tyler, Matthew A et al. (2013) Noggin attenuates cerulein-induced acute pancreatitis and impaired autophagy. Pancreas 42:301-7
Okamura, Daiki; Starr, Marlene E; Lee, Eun Y et al. (2012) Age-dependent vulnerability to experimental acute pancreatitis is associated with increased systemic inflammation and thrombosis. Aging Cell 11:760-9

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