The purpose of the proposed Islet Cell and Functional Analysis Core (IFAC) is to stimulate and support research involving the physiologic and pathophysiologic role of pancreatic islets, both by preparing and maintaining islet experimental models and providing the analytical tools to analyze their function. The IFAC will be an expansion of the Islet Cell Satellite (ICS) that since 1991 has been under the auspices of the Cell and Tissue Core. The increased interest in islet research and the maturation of the satellite warrants that the ICS be reclassified administratively as a separate Core and its resources expanded. The major focus of the Core is preparation of islets for Affiliate Investigator's projects, functional evaluation including quality assurance, and the development of novel functional assessment technologies. The Islet Cell Satellite currently supports about 15 investigator's research; however, expansion of services and resources will likely increase this number to more than 20. Overall, the scope of services that IFAC will provide are 1) production of islets and islet-related materials; 2) a central resource for the procurement of human and non-human primate tissues and organs; 3) maintenance of islet tissue in culture; 4) acute and chronic functional assessment of islets using biochemical and imaging technology; 5) and training of staff and consultation in islet and islet cell work. The provision of these resources will play an integral part in facilitating islet-based research in the numerous institutes research centers in the Seattle area.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK017047-28
Application #
7550714
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2003-12-01
Budget End
2004-11-30
Support Year
28
Fiscal Year
2004
Total Cost
$135,374
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Mukamal, Kenneth J; Siscovick, David S; de Boer, Ian H et al. (2018) Metabolic Clusters and Outcomes in Older Adults: The Cardiovascular Health Study. J Am Geriatr Soc 66:289-296
Wall, Valerie Z; Barnhart, Shelley; Kanter, Jenny E et al. (2018) Smooth muscle glucose metabolism promotes monocyte recruitment and atherosclerosis in a mouse model of metabolic syndrome. JCI Insight 3:
Toledo, Frederico G S; Johannsen, Darcy L; Covington, Jeffrey D et al. (2018) Impact of prolonged overfeeding on skeletal muscle mitochondria in healthy individuals. Diabetologia 61:466-475
Ferreccio, Amy; Mathieu, Julie; Detraux, Damien et al. (2018) Inducible CRISPR genome editing platform in naive human embryonic stem cells reveals JARID2 function in self-renewal. Cell Cycle 17:535-549
Bornfeldt, Karin E; Kramer, Farah; Batorsky, Anna et al. (2018) A Novel Type 2 Diabetes Mouse Model of Combined Diabetic Kidney Disease and Atherosclerosis. Am J Pathol 188:343-352
Tang, Jingjing; Frey, Jeremy M; Wilson, Carole L et al. (2018) Neutrophil and macrophage cell surface CSF-1 shed by ADAM17 drives mouse macrophage proliferation in acute and chronic inflammation. Mol Cell Biol :
Lynch, Kristian F; Lee, Hye-Seung; Törn, Carina et al. (2018) Gestational respiratory infections interacting with offspring HLA and CTLA-4 modifies incident ?-cell autoantibodies. J Autoimmun 86:93-103
Parilla, Jacqueline H; Willard, Joshua R; Barrow, Breanne M et al. (2018) A Mouse Model of Beta-Cell Dysfunction as Seen in Human Type 2 Diabetes. J Diabetes Res 2018:6106051
Elding Larsson, Helena; Lynch, Kristian F; Lönnrot, Maria et al. (2018) Pandemrix® vaccination is not associated with increased risk of islet autoimmunity or type 1 diabetes in the TEDDY study children. Diabetologia 61:193-202
Wang, Ke; Zelnick, Leila R; Hoofnagle, Andrew N et al. (2018) Alteration of HDL Protein Composition with Hemodialysis Initiation. Clin J Am Soc Nephrol 13:1225-1233

Showing the most recent 10 out of 1296 publications