Human pancreatic islets are an essential research resource allowing for the translation of fundamental questions related to the prevention, treatment, and pathophysiology of diabetes mellitus. Recent data has highlighted important differences between islets from animal models and human islets, substantiating the continued need for researcher access to human islets. However, several challenges exist in maintaining and enhancing the necessary infrastructure and coordinating function to effectively and efficiently distribute this precious resource to islet research laboratories. City of Hope (COH) is applying for this UC4 renewal to remain the Coordinating Center (CC) to support the Integrated Islet Distribution Program (IIDP) that provides for the distribution of human cadaveric islets for biomedical research to researchers worldwide. Our proposal leverages the significant investment made by NIH over the last 12 years that has established and successfully maintained this islet distribution network at COH. From qualification and auditing of high-quality suppliers to forecasting, tracking, and meeting the needs of investigators, our experienced IIDP-CC team has worked with 19 different isolation laboratories to coordinate the distribution of over 231 million islet equivalents to 316 investigative studies over a period of more than 14 years, facilitating the completion of 499 publications. As the ongoing IIDP-CC, we will continue to subcontract with qualified islet isolation facilities to prepare and distribute human islets through our advanced electronic Islet Allocation System. As the IIDP-CC, we will continue to manage the review process for IIDP applications to establish investigator eligibility for islet receipt (including opportunity pool submissions), maintain investigator rosters, and further enhance our IAS that allows distribution centers to broadcast offers online and notifies approved waiting researchers of islet availability. We will continue to maintain the existing cost recovery system through subscription fees collected from islet researchers, which has successfully garnered approximately $3,000,000 under the existing grant to offset the expenses of pancreatic processing. We will continue to closely monitor and help to improve the quality of islets distributed, through the continuation of a Quality Control Core Facility that tests a sample from each islet isolation using agreed upon quality control assays. Quality control data, as well as extensive donor and islet isolation data, will be made available to approved investigators through online access. Through our proven state-of-the-art administrative, business, technical, statistical, quality assurance, and informatics processes and tools, this project will benefit from COH?s advanced systems, and the accessibility of human islets for investigators conducting essential diabetes mellitus research will be secured. Through the aims described in this proposal, we will provide an indispensable research resource for the diabetes research community by ensuring that the IIDP network remains stable, technologically advanced, continually enhanced, and fully responsive to the islet needs of the research community, thus promoting the next generation of scientific experimentation toward prevention and treatment of diabetes.

Public Health Relevance

Individuals with diabetes experience significant primary and secondary complications, costing an estimated annual $322 billion dollars of care in the United States. The central importance of human islets in the pathology of this disease, and demonstrated use of islets as an unparalleled experimental and treatment resource, has led to continued demand for islets from healthy donors, and an escalating demand for specific islet preparations from donors with Type 2 Diabetes and rare diseases. Maintenance of a large scale islet distribution network is critical to provide researchers with access to this precious resource, advancing the discoveries and progress in the field of diabetes mellitus research.

Project Start
2012-09-30
Project End
2022-03-31
Budget Start
2017-07-01
Budget End
2022-03-31
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Beckman Research Institute/City of Hope
Department
Type
DUNS #
027176833
City
Duarte
State
CA
Country
United States
Zip Code
91010
Khetan, Shubham; Kursawe, Romy; Youn, Ahrim et al. (2018) Type 2 Diabetes-Associated Genetic Variants Regulate Chromatin Accessibility in Human Islets. Diabetes 67:2466-2477
Kong, Yahui; Ebrahimpour, Pantea; Liu, Yu et al. (2018) Pancreatic Islet Embedding for Paraffin Sections. J Vis Exp :
Saunders, Diane C; Brissova, Marcela; Phillips, Neil et al. (2018) Ectonucleoside Triphosphate Diphosphohydrolase-3 Antibody Targets Adult Human Pancreatic ? Cells for In Vitro and In Vivo Analysis. Cell Metab :
Jiang, K; Chaimov, D; Patel, S N et al. (2018) 3-D physiomimetic extracellular matrix hydrogels provide a supportive microenvironment for rodent and human islet culture. Biomaterials :
Lakhter, Alexander J; Pratt, Rachel E; Moore, Rachel E et al. (2018) Beta cell extracellular vesicle miR-21-5p cargo is increased in response to inflammatory cytokines and serves as a biomarker of type 1 diabetes. Diabetologia 61:1124-1134
Wong, Winifred P; Allen, Norrina B; Meyers, Matthew S et al. (2017) Exploring the Association Between Demographics, SLC30A8 Genotype, and Human Islet Content of Zinc, Cadmium, Copper, Iron, Manganese and Nickel. Sci Rep 7:473
Zhang, Yanqing; Wu, Meifen; Htun, Wynn et al. (2017) Differential Effects of Linagliptin on the Function of Human Islets Isolated from Non-diabetic and Diabetic Donors. Sci Rep 7:7964
Li, Jin; Casteels, Tamara; Frogne, Thomas et al. (2017) Artemisinins Target GABAA Receptor Signaling and Impair ? Cell Identity. Cell 168:86-100.e15
Yoshimatsu, Gumpei; Kunnathodi, Faisal; Saravanan, Prathab Balaji et al. (2017) Pancreatic ?-Cell-Derived IP-10/CXCL10 Isletokine Mediates Early Loss of Graft Function in Islet Cell Transplantation. Diabetes 66:2857-2867
Messenger, Scott W; Thomas, Diana Dh; Cooley, Michelle M et al. (2015) Early to Late Endosome Trafficking Controls Secretion and Zymogen Activation in Rodent and Human Pancreatic Acinar Cells. Cell Mol Gastroenterol Hepatol 1:695-709

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