The Islet Procurement and Analysis Core is a new core of the Vanderbilt DRTC. Islet biology, development, and function are major DRTC research areas with investigators studying a variety of islet-related processes ranging from intracellular signaling, the immunology of type 1 diabetes, islet-enriched transcription factors, to islet transplantation. Central to many experimental paradigms of these DRTC-affiliated investigators is access to rodent, porcine, or human pancreatic islets. The objective of this core is to facilitate the research of DRTC-affiliated investigators by providing high quality, well-characterized pancreatic islets and to assist investigators in studies that use these islets. A mouse islet isolation core at Vanderbilt has been operational under the auspices of the Vanderbilt Mouse Metabolic Phenotyping Center (MMPC), but its design is such that it is not well-suited for handling the volume of islets needed as the number and activity of DRTC investigators within Vanderbilt continue to grow. In addition, a number of Vanderbilt researchers are studying the mechanisms involved in mouse islet development and function, but limited access to human islets slows translation of their observations into the human islet arena. Thus, in this application, we propose to create the Vanderbilt Islet Procurement and Analysis Core, which will be jointly supported by the NIDDK-funded MMPC and the DRTC and will substantially increase the access of DRTC-affiliated investigators to pancreatic islets. The services offered by this core are: 1) isolation of rodent pancreatic islets;2) purification and handling of human islets (received from NIH/JDRF human islet distribution program);and 3) characterization of islet preparations from all species by assessment of insulin secretion in a cell perifusion system. This core will expand the ability of DRTC-affiliated investigators to perform diabetes-related research and will interact with other DRTC-supported cores. For example, isolated islets may be studied in the Cell Imaging Shared Resource, secreted islet hormones would be assayed in the Hormone Assay Core, or parallel studies assessing in vivo insulin secretion can be performed in the Metabolic Physiology Shared Resource and correlated with in vitro studies in isolated islets. This core will provide essential services that support the research of DRTC-affiliated investigators in the next funding cycle.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Comprehensive Center (P60)
Project #
5P60DK020593-33
Application #
8281520
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2011-04-01
Budget End
2012-03-31
Support Year
33
Fiscal Year
2011
Total Cost
$84,335
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Lockhart, Jacob N; Spoonmore, Thomas J; McCurdy, Michael W et al. (2018) Poly(glycidol) Coating on Ultrahigh Molecular Weight Polyethylene for Reduced Biofilm Growth. ACS Appl Mater Interfaces 10:4050-4056
Shropshire, J Dylan; On, Jungmin; Layton, Emily M et al. (2018) One prophage WO gene rescues cytoplasmic incompatibility in Drosophila melanogaster. Proc Natl Acad Sci U S A 115:4987-4991
Sucre, Jennifer M S; Deutsch, Gail H; Jetter, Christopher S et al. (2018) A Shared Pattern of ?-Catenin Activation in Bronchopulmonary Dysplasia and Idiopathic Pulmonary Fibrosis. Am J Pathol 188:853-862
Schlegel, Cameron; Weis, Victoria G; Knowles, Byron C et al. (2018) Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease. Dig Dis Sci 63:356-365
Wilson, Christopher S; Chhabra, Preeti; Marshall, Andrew F et al. (2018) Healthy Donor Polyclonal IgMs Diminish B-Lymphocyte Autoreactivity, Enhance Regulatory T-Cell Generation, and Reverse Type 1 Diabetes in NOD Mice. Diabetes 67:2349-2360
Hughey, Curtis C; Trefts, Elijah; Bracy, Deanna P et al. (2018) Glycine N-methyltransferase deletion in mice diverts carbon flux from gluconeogenesis to pathways that utilize excess methionine cycle intermediates. J Biol Chem 293:11944-11954
Yao, Lina; Seaton, Sarah Craven; Ndousse-Fetter, Sula et al. (2018) A selective gut bacterial bile salt hydrolase alters host metabolism. Elife 7:
Mani, Bharath K; Castorena, Carlos M; Osborne-Lawrence, Sherri et al. (2018) Ghrelin mediates exercise endurance and the feeding response post-exercise. Mol Metab 9:114-130
Bolus, W Reid; Peterson, Kristin R; Hubler, Merla J et al. (2018) Elevating adipose eosinophils in obese mice to physiologically normal levels does not rescue metabolic impairments. Mol Metab 8:86-95
West, Kathryn L; Kelm, Nathaniel D; Carson, Robert P et al. (2018) Myelin volume fraction imaging with MRI. Neuroimage 182:511-521

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