Renal injury triggers complicated molecular, cellular, and physiological responses difficult to study using conventional technology. Transcription profiling - a genome-scale determination of gene expression - is a promising new technology that might allow us to obtain quantitative information about the complex transcription profiles (i.e., transcriptome) that underlie renal failure. We will use high-density microarrays to map glomerular gene expression in a murine model of diabetic nephropathy. Specif?c Aim 1 will map expression of>l 1,000 genes in freshly isolated glomeruli from db/db mice. We chose the db/db mouse model because it develops progressive renal insufficiency with features of type II diabetic nephropathy in humans. The gene expression profile will be constructed at an early stage when mice are hyperglycemic, but with little evidence of renal injury, and at a later stage characterized by overt diabetic nephropathy. In addition to identifying known and unknown genes differentially regulated in diabetic renal injury, we will used unsupervised and supervised learning tools to gain biological insight into the gene expression profiles.
Specific Aim 2 will identify candidate genes linked to diabetic nephropathy by treating db/db mice with an angiotensin (ANG 11)-converting enzyme inhibitor, an anti-transforming growth factor Beta (TGFBeta) antibody, and both therapies combined.
Aim 2 will thus identify transcription profiles altered by blocking ANG II and TGFBeta. These experiments will also discover genes altered in diabetes that are not affected by therapy and thus possibly linked to diabetic glomeruloscierosis. This pilot project will test the feasibility of transcription profiling to identify novel target genes for future mechanistic investigations into glomerular remodeling in diabetic nephropathy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21DK062331-01
Application #
6532146
Study Section
General Medicine B Study Section (GMB)
Program Officer
Meyers, Catherine M
Project Start
2002-09-01
Project End
2004-06-30
Budget Start
2002-09-01
Budget End
2003-06-30
Support Year
1
Fiscal Year
2002
Total Cost
$153,000
Indirect Cost
Name
Case Western Reserve University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Mishra, Rangnath; Emancipator, Steven N; Kern, Timothy S et al. (2006) Association between endothelin-1 and collagen deposition in db/db diabetic mouse kidneys. Biochem Biophys Res Commun 339:65-70
Mishra, Rangnath; Emancipator, Steven N; Kern, Timothy et al. (2005) High glucose evokes an intrinsic proapoptotic signaling pathway in mesangial cells. Kidney Int 67:82-93
Mishra, Rangnath; Emancipator, Steven N; Miller, Casey et al. (2004) Adipose differentiation-related protein and regulators of lipid homeostasis identified by gene expression profiling in the murine db/db diabetic kidney. Am J Physiol Renal Physiol 286:F913-21