The goals of the University of Michigan George M. O'Brien Renal and Urologic Center are to promote research into questions of importance to the kidney and urologic community, to exchange ideas and information about these areas, and to recruit new individuals to work in kidney and urologic diseases. Good progress has been made in the prior four years of support in each of these areas. Exciting individual research accomplishments set the scene for the current research proposals. These include addressing the following questions: a) the mechanism by which glycine protects cells against various types of injury; b) the regulation of tubular cell differentiation; c) type IV collagen gene regulation: d) looking for the function of newly cloned, sequenced and expressed endothelial cell cytokine: e) cloning, sequencing and defining the role of a new glomerular epithelial cell protein; f) defining the contribution of adhesion proteins and cytokines to acute glomerular injury; g) using novel inhibitors of glycosphingolipid synthesis to define their effects and potential for clinical use on renal carcinoma cell surface adhesion protein expression and metastatic potential; h) defining the interactions of glucose transporters, ATP-sensitive potassium channels and purinergic receptors on afferent arteriolar tone and renin secretion using quantitative PCR and other approaches. These individual projects will form the core and critical mass about which the activities of the Center revolve with respect to its' other important functions of teaching/exchange of information and recruiting young investigators into kidney/urologic research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Specialized Center (P50)
Project #
5P50DK039255-07
Application #
3105859
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1987-09-01
Project End
1997-07-31
Budget Start
1993-08-01
Budget End
1994-07-31
Support Year
7
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Hato, Takashi; Winfree, Seth; Day, Richard et al. (2017) Two-Photon Intravital Fluorescence Lifetime Imaging of the Kidney Reveals Cell-Type Specific Metabolic Signatures. J Am Soc Nephrol 28:2420-2430
Kikuchi, Masao; Wickman, Larysa; Hodgin, Jeffrey B et al. (2015) Podometrics as a Potential Clinical Tool for Glomerular Disease Management. Semin Nephrol 35:245-55
Yu, Fa-Xing; Zhao, Bin; Guan, Kun-Liang (2015) Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer. Cell 163:811-28
Fukuda, Akihiro; Wickman, Larysa T; Venkatareddy, Madhusudan P et al. (2012) Urine podocin:nephrin mRNA ratio (PNR) as a podocyte stress biomarker. Nephrol Dial Transplant 27:4079-87
Fukuda, Akihiro; Wickman, Larysa T; Venkatareddy, Madhusudan P et al. (2012) Angiotensin II-dependent persistent podocyte loss from destabilized glomeruli causes progression of end stage kidney disease. Kidney Int 81:40-55
Wiggins, Jocelyn E (2012) Aging in the glomerulus. J Gerontol A Biol Sci Med Sci 67:1358-64
Fukuda, Akihiro; Chowdhury, Mahboob A; Venkatareddy, Madhusudan P et al. (2012) Growth-dependent podocyte failure causes glomerulosclerosis. J Am Soc Nephrol 23:1351-63
Chernin, Gil; Heeringa, Saskia F; Vega-Warner, Virginia et al. (2010) Adequate use of allele frequencies in Hispanics--a problem elucidated in nephrotic syndrome. Pediatr Nephrol 25:261-6
Chernin, Gil; Vega-Warner, Virginia; Schoeb, Dominik S et al. (2010) Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations. Clin J Am Soc Nephrol 5:1655-62
Kim, Doyeob; Patel, Sanjeevkumar R; Xiao, Hong et al. (2009) The role of PTIP in maintaining embryonic stem cell pluripotency. Stem Cells 27:1516-23

Showing the most recent 10 out of 189 publications