Over the last 15 years, our group has successfully managed the coordinating and bioinformatics unit (CBU) for two NIDDK funded consortia, the Diabetic Complications Consortium (DiaComp 2001-present, formerly the Animal Models of Diabetic Complications Consortium) and the Mouse Metabolic Phenotyping Centers (MMPC, 2006-present). DiaComp provides an environment to foster communications and collaborations between investigator communities involved in diabetic complications research. Toward this goal, DiaComp sponsors annual meetings in complications-relevant scientific areas, solicits and funds pilot projects in high impact areas of complications research, and supports a website to serve the diabetic complications community. During the current five year funding cycle, the CBU was responsible for continuing support for DiaComp through the use of opportunity pools (funding), manage/maintain the website and phenotyping data and administratively organize the meetings and workshops sponsored by the DiaComp to engage the greater diabetic complications scientific community. In contrast, the MMPCs are charged with providing the scientific community with standardized, high quality metabolic and physiologic phenotyping services for the mouse. The MMPC provides state-of-the-art technologies to investigators for a fee, with their services including characterization of mouse metabolism, blood composition (including hormones), energy balance, eating and exercise, organ function and morphology, physiology and histology. Over the last ten years the two consortia have been managed by one CBU because of the NIH decision to integrate the activities of the two consortia during their second funding cycles. Our laboratory has been the CBU for both DiaComp (last 15 years) and the MMPC (last 10 years). The CBU is responsible for creating and maintaining the administrative, scientific and informatics infrastructure necessary to organize and facilitate their operations. The goal of this proposal is to provide that infrastructure. We will build upon the success of the current DiaComp/MMPC CBU infrastructure to provide both DiaComp and MMPC with a robust and comprehensive service oriented solution that supports both the common and unique aspects of each.

Public Health Relevance

The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) is providing funds to establish the coordinating and bioinformatics unit (CBU) for the Mouse Metabolic Phenotyping Centers (MMPC) and Diabetic Complications Consortium (DiaComp) programs. The CBU will coordinate the interactions of the MMPC Center awardees, provide financial management for opportunity pool programs, interact with the Executive Steering Committees and External Evaluation Committees as well as provide national web portals for both the MMPC and DiaComp programs in order to disseminate information and provide an organizational infrastructure for the program. This application will provide the infrastructure for the CBU for the MMPC and DiaComp.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
2U24DK076169-11
Application #
9172351
Study Section
Special Emphasis Panel (ZDK1-GRB-7 (M2)S)
Program Officer
Abraham, Kristin M
Project Start
2006-09-15
Project End
2017-07-31
Budget Start
2016-08-29
Budget End
2017-07-31
Support Year
11
Fiscal Year
2016
Total Cost
$3,590,563
Indirect Cost
$776,177
Name
Georgia Regents University
Department
Pathology
Type
Schools of Medicine
DUNS #
City
Augusta
State
GA
Country
United States
Zip Code
30912
Mitrofanova, Alla; Molina, Judith; Varona Santos, Javier et al. (2018) Hydroxypropyl-?-cyclodextrin protects from kidney disease in experimental Alport syndrome and focal segmental glomerulosclerosis. Kidney Int 94:1151-1159
Winfree, Seth; Dagher, Pierre C; Dunn, Kenneth W et al. (2018) Quantitative Large-Scale Three-Dimensional Imaging of Human Kidney Biopsies: A Bridge to Precision Medicine in Kidney Disease. Nephron 140:134-139
Forney, Laura A; Stone, Kirsten P; Wanders, Desiree et al. (2018) Sensing and signaling mechanisms linking dietary methionine restriction to the behavioral and physiological components of the response. Front Neuroendocrinol 51:36-45
Chozinski, Tyler J; Mao, Chenyi; Halpern, Aaron R et al. (2018) Volumetric, Nanoscale Optical Imaging of Mouse and Human Kidney via Expansion Microscopy. Sci Rep 8:10396
Widlansky, Michael E; Jensen, David M; Wang, Jingli et al. (2018) miR-29 contributes to normal endothelial function and can restore it in cardiometabolic disorders. EMBO Mol Med 10:
Jahan, Ishrat; Corbin, Kathryn L; Bogart, Avery M et al. (2018) Reducing Glucokinase Activity Restores Endogenous Pulsatility and Enhances Insulin Secretion in Islets From db/db Mice. Endocrinology 159:3747-3760
Wu, Haojia; Malone, Andrew F; Donnelly, Erinn L et al. (2018) Single-Cell Transcriptomics of a Human Kidney Allograft Biopsy Specimen Defines a Diverse Inflammatory Response. J Am Soc Nephrol 29:2069-2080
Cheng, Yingduan; Yuan, Quan; Vergnes, Laurent et al. (2018) KDM4B protects against obesity and metabolic dysfunction. Proc Natl Acad Sci U S A 115:E5566-E5575
Mina, Amir I; LeClair, Raymond A; LeClair, Katherine B et al. (2018) CalR: A Web-Based Analysis Tool for Indirect Calorimetry Experiments. Cell Metab 28:656-666.e1
Wang, Feng; Katagiri, Daisuke; Li, Ke et al. (2018) Assessment of renal fibrosis in murine diabetic nephropathy using quantitative magnetization transfer MRI. Magn Reson Med 80:2655-2669

Showing the most recent 10 out of 181 publications