Bone morphogenic proteins (BMPs) are members of the transforming growth factor (TGF) beta super family of growth factors that regulate many physiologic and pathyphysiologic processes in the kidney including nephrogenesis, response to injury, and repair. Although their precise role in the kidney is still not fully understood, BMPs appear be protective against renal injury to a variety of insults including ischemia, obstruction, and diabetes mellitus. Dragon is a novel GPI-anchored membrane protein, which has recently been identified. Preliminary data will be presented which demonstrates that Dragon is involved in BMP signaling, and that Dragon is expressed in the kidney in renal tubular epithelial cells which are relatively protected against ischemic injury. This proposal will investigate further the precise role of Dragon in BMP signaling and elucidate the molecular and cellular mechanisms involved. Proposed experiments will also begin to examine the functional significance of Dragon expression in the kidney in relation to ischemic injury and repair. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DK068997-02
Application #
6951049
Study Section
Special Emphasis Panel (ZRG1-F10 (21))
Program Officer
Rankin, Tracy L
Project Start
2004-07-01
Project End
2006-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
2
Fiscal Year
2005
Total Cost
$54,352
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Babitt, Jodie L; Huang, Franklin W; Wrighting, Diedra M et al. (2006) Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression. Nat Genet 38:531-9
Babitt, Jodie L; Zhang, Ying; Samad, Tarek A et al. (2005) Repulsive guidance molecule (RGMa), a DRAGON homologue, is a bone morphogenetic protein co-receptor. J Biol Chem 280:29820-7