The Iowa Diabetes and Endocrinology Research Center (DERC) is designed to foster a multidisciplinary approach to the study of diabetes and hormone action at the cellular and molecular level. Investigations primarily relate to insulin, IGFs and glucose transporters but also include investigation of cellular effects of steroid hormones, GnRH, prolactin, CGRP, LH/FSH and growth factors (glia maturation factor, TGF-beta, cytokines). The Center has five major goals: 1) to develop molecular biology approaches to diabetes and hormone action research; 2) to centralize facilities that were being duplicated in several different laboratories; 3) to provide, as core resources, facilities and expertise that are not available at the University and permit new areas of investigation by multiple DERC investigators; 4) to test new hypotheses related to diabetes and mechanisms of hormone action through the Pilot and Feasibility Program; and 5) to promote multidisciplinary approaches to the study of diabetes and hormone action through collaborative studies. To achieve these goals, the Center has developed several resources: An Administrative Core; Molecular Biology Core (Recombinant DNA and DNA Synthesis); Cell Biology Core (Media and Protein Production); Membrane Biology Core (Central Facility for Peptide Iodination, Signal Transduction Analysis and In situ Hybridization); a Pilot and Feasibility Study Program to support pilot studies related to the Center theme; a Computer Core; and an Enrichment Program of seminar speakers and workshops.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK025295-15
Application #
2137695
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1979-04-01
Project End
1997-11-30
Budget Start
1994-02-10
Budget End
1994-11-30
Support Year
15
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Harding, Anne Marie S; Kusama, Nobuyoshi; Hattori, Tomonori et al. (2014) ASIC2 subunits facilitate expression at the cell surface and confer regulation by PSD-95. PLoS One 9:e93797
Kusama, Nobuyoshi; Gautam, Mamta; Harding, Anne Marie S et al. (2013) Acid-sensing ion channels (ASICs) are differentially modulated by anions dependent on their subunit composition. Am J Physiol Cell Physiol 304:C89-101
Collier, Daniel M; Peterson, Zerubbabel J; Blokhin, Ilya O et al. (2012) Identification of extracellular domain residues required for epithelial Na+ channel activation by acidic pH. J Biol Chem 287:40907-14
Herlein, Judith A; Fink, Brian D; Henry, Dorlyne M et al. (2011) Mitochondrial superoxide and coenzyme Q in insulin-deficient rats: increased electron leak. Am J Physiol Regul Integr Comp Physiol 301:R1616-24
Herlein, Judy A; Fink, Brian D; Sivitz, William I (2010) Superoxide production by mitochondria of insulin-sensitive tissues: mechanistic differences and effect of early diabetes. Metabolism 59:247-57
Sivitz, William I; Yorek, Mark A (2010) Mitochondrial dysfunction in diabetes: from molecular mechanisms to functional significance and therapeutic opportunities. Antioxid Redox Signal 12:537-77
Elliott, David E; Weinstock, Joel V (2009) Helminthic therapy: using worms to treat immune-mediated disease. Adv Exp Med Biol 666:157-66
Herlein, Judith A; Fink, Brian D; O'Malley, Yunxia et al. (2009) Superoxide and respiratory coupling in mitochondria of insulin-deficient diabetic rats. Endocrinology 150:46-55
Hattori, Tomonori; Chen, Jie; Harding, Anne Marie S et al. (2009) ASIC2a and ASIC3 heteromultimerize to form pH-sensitive channels in mouse cardiac dorsal root ganglia neurons. Circ Res 105:279-86
Fink, Brian D; O'Malley, Yunxia; Dake, Brian L et al. (2009) Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells. PLoS One 4:e4250

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