This project will evaluate the putative role of hepatic sinusoidal endothelial xanthine oxidase as an inflammatory signal transduction mechanism, transducing circulating proinflammatory signals (TNFalpha, gammaINF, endotoxin [LPS]) by virtue of oxidant generation causing the upregulation of endothelial surface adhesion molecules, and the consequent arrest, trapping and activation of circulating neutrophils, a mechanism to effect phagocytic killing of microorganisms, an essential component of reticuloendothelial system function. Specifically, this project will study this in the intact organism, in real time using a combination of intravital microscopy of the rat liver in vivo, intravital microscopy of the isolated perfused rat liver ex vivo, and histologic and histochemical evaluation of livers taken from intact living rats treated in vivo. This project will focus on identifying the response to the above proinflammatory agonists, the identification of the adhesion molecules expressed, establishment of the role of xanthine oxidase-generated oxidants and the role of intercellular calcium fluxes in triggering this response. Studies will be conducted in the laboratories of Drs. Gregory Bulkley, Mark Clemens and marshall Montrose. When combined with a focused program of course work, this two year fellowship should thereby provide sound fundamental background for a subsequent career in academic general surgery, following the completion of clinical training.

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 #
5F32DK009493-02
Application #
2443888
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Program Officer
Podskalny, Judith M,
Project Start
1997-07-01
Project End
Budget Start
1997-07-01
Budget End
1998-06-30
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Surgery
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
You, Hanning; Gao, Ting; Cooper, Timothy K et al. (2015) Arginase inhibition: a new treatment for preventing progression of established diabetic nephropathy. Am J Physiol Renal Physiol 309:F447-55
Awad, Alaa S; You, Hanning; Gao, Ting et al. (2015) Delayed Treatment with a Small Pigment Epithelium Derived Factor (PEDF) Peptide Prevents the Progression of Diabetic Renal Injury. PLoS One 10:e0133777
Awad, Alaa S; You, Hanning; Gao, Ting et al. (2015) Macrophage-derived tumor necrosis factor-? mediates diabetic renal injury. Kidney Int 88:722-33
You, Hanning; Gao, Ting; Cooper, Timothy K et al. (2014) Diabetic nephropathy is resistant to oral L-arginine or L-citrulline supplementation. Am J Physiol Renal Physiol 307:F1292-301