ISLET CELL BIOLOGY CORE: Director - F. MatschinskyIt is the purpose of this core to assist investigators who currently study or have plans to studyindependently or collaboratively various aspects of pancreatic islet cell biology. In order toaccomplish this goal the Core provides four services. First, it will perform extra corporalphenotyping of the endocrine pancreas of mouse and rat using the intact isolated perfused orminced perifused pancreas. Second, it will isolate, culture, and functionally assess pancreatic isletsof rat and mouse including batch incubations, perifusions, respirometry, measurements of Caj++, theP-potential (ATP, ADP, AMP and Pi) and other metabolites, hormone contents and release. Third, itmaintains a broad and well characterized stock of transformed islet cells, grows large batches ofsuch cells or generates pseudo islets by embedding such cells into agarose beads for dynamicstudies of metabolism and hormone release. Fourth and most important, it provides in depthconsultation and helps develop strategies how to use the services of the core optimally or willattempt to modify available technologies to solve particular problems. The islet cell resource permitsthe broad application of approaches which are too labor intensive and technically too demanding tobe maintained by the average single laboratory. The core offers training to those who have theresources and wish to establish approved procedures and technologies in their own laboratory.Costs are reduced through a large scale operation. The Core functions thus as a research supportand educational unit for an active group of investigators with somewhat diverse interests, andfosters interdisciplinary islet research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK019525-31
Application #
7283872
Study Section
Special Emphasis Panel (ZDK1-GRB-N (J1))
Project Start
2007-04-01
Project End
2012-03-31
Budget Start
2007-05-15
Budget End
2008-03-31
Support Year
31
Fiscal Year
2007
Total Cost
$168,188
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Rickels, Michael R; Peleckis, Amy J; Dalton-Bakes, Cornelia et al. (2018) Continuous Glucose Monitoring for Hypoglycemia Avoidance and Glucose Counterregulation in Long-Standing Type 1 Diabetes. J Clin Endocrinol Metab 103:105-114
Guan, Dongyin; Xiong, Ying; Borck, Patricia C et al. (2018) Diet-Induced Circadian Enhancer Remodeling Synchronizes Opposing Hepatic Lipid Metabolic Processes. Cell 174:831-842.e12
Jang, Cholsoon; Chen, Li; Rabinowitz, Joshua D (2018) Metabolomics and Isotope Tracing. Cell 173:822-837
Shoshkes-Carmel, Michal; Wang, Yue J; Wangensteen, Kirk J et al. (2018) Subepithelial telocytes are an important source of Wnts that supports intestinal crypts. Nature 557:242-246
Ibrahim, Fadia; Maragkakis, Manolis; Alexiou, Panagiotis et al. (2018) Ribothrypsis, a novel process of canonical mRNA decay, mediates ribosome-phased mRNA endonucleolysis. Nat Struct Mol Biol 25:302-310
Cooney, Laura G; Milman, Lauren W; Hantsoo, Liisa et al. (2018) Cognitive-behavioral therapy improves weight loss and quality of life in women with polycystic ovary syndrome: a pilot randomized clinical trial. Fertil Steril 110:161-171.e1
Condon, David E; Tran, Phu V; Lien, Yu-Chin et al. (2018) Defiant: (DMRs: easy, fast, identification and ANnoTation) identifies differentially Methylated regions from iron-deficient rat hippocampus. BMC Bioinformatics 19:31
Correnti, Jason M; Gottshall, Lauren; Lin, Annie et al. (2018) Ethanol and C2 ceramide activate fatty acid oxidation in human hepatoma cells. Sci Rep 8:12923
Williams, Bianca; Correnti, Jason; Oranu, Amanke et al. (2018) A novel role for ceramide synthase 6 in mouse and human alcoholic steatosis. FASEB J 32:130-142
Qiu, Chengxiang; Huang, Shizheng; Park, Jihwan et al. (2018) Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. Nat Med 24:1721-1731

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