? Obstruction of the upper urinary tract is a major clinical problem in both children and adults that results in progressive and ultimately irreversible renal damage. The majority of obstructive renal injury is attributed to renal cell loss via apoptosis and to progressive renal fibrosis. A number of inflammatory mediators have been implicated in the pathophysiology of renal obstruction, including tumor necrosis factor (TNF). TNF is a known cytotoxic agent capable of inducing apoptotic renal cell death in ischemic models of renal injury. While increased expression of TNF has been demonstrated following renal obstruction, the role of TNF in obstruction-induced renal cell apoptosis and fibrosis has not been elucidated. Our long term objectives are therefore to identify TNF as an important mediator of apoptosis and renal fibrosis during obstruction, and further, to develop a clinically relevant therapeutic strategy that will limit or prevent TNF induced obstructive renal injury. These goals will be accomplished using a rat model of unilateral renal obstruction by 1) determining the time course of renal cell apoptosis and fibrosis during obstruction, 2) determining the role of TNF in obstruction-induced renal apoptosis and fibrosis using the specific TNF inhibitor, soluble TNF receptor I (RTBP1), and 3) investigating the mechanisms of obstruction-induced renal TNF expression.
For Specific Aim I, renal cortical tissue wilt be harvested following 1, 3, 7, or 14 days of obstruction, and assessed with regards to TNF expression and activity, TGF-beta expression, collagen deposition and fibrosis, and degree of apoptosis.
Specific Aim II will assess the impact of TNF inhibition on obstruction-induced renal injury by investigating the parameters outlined in Aim I using rats that have been exposed to RTBP1 during the period of obstruction.
Specific Aim III will assess the mechanisms of obstruction-induced renal TNF expression by investigating known regulators of TNF production, including nuclear factor kappaB and p38 mitogen activated protein kinase. Overall, the objective of this proposal is to apply and enhance the knowlegde gained by the applicant during her residency and fellowship training to develop a clinically relevant therapeutic approach to the treatment and prevention of obstructive renal injury ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08DK065892-02
Application #
6926964
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Rankin, Tracy L
Project Start
2004-08-01
Project End
2009-07-31
Budget Start
2005-08-01
Budget End
2006-07-31
Support Year
2
Fiscal Year
2005
Total Cost
$133,378
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Urology
Type
Schools of Medicine
DUNS #
603007902
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Campbell, Matthew T; Hile, Karen L; Zhang, Hongji et al. (2011) Toll-like receptor 4: a novel signaling pathway during renal fibrogenesis. J Surg Res 168:e61-9
Zhang, Hongji; Hile, Karen L; Asanuma, Hiroshi et al. (2011) IL-18 mediates proapoptotic signaling in renal tubular cells through a Fas ligand-dependent mechanism. Am J Physiol Renal Physiol 301:F171-8
Bani-Hani, Ahmad H; Leslie, Jeffery A; Asanuma, Hiroshi et al. (2009) IL-18 neutralization ameliorates obstruction-induced epithelial-mesenchymal transition and renal fibrosis. Kidney Int 76:500-11
Wang, Meijing; Tan, Jiangning; Wang, Yue et al. (2009) IL-18 binding protein-expressing mesenchymal stem cells improve myocardial protection after ischemia or infarction. Proc Natl Acad Sci U S A 106:17499-504
Campbell, Matthew T; Dagher, Pierre; Hile, Karen L et al. (2008) Tumor necrosis factor-alpha induces intrinsic apoptotic signaling during renal obstruction through truncated bid activation. J Urol 180:2694-700
Metcalfe, Peter D; Leslie, Jeffrey A; Campbell, Matthew T et al. (2008) Testosterone exacerbates obstructive renal injury by stimulating TNF-alpha production and increasing proapoptotic and profibrotic signaling. Am J Physiol Endocrinol Metab 294:E435-43
Wang, Meijing; Zhang, Wenjun; Crisostomo, Paul et al. (2007) STAT3 mediates bone marrow mesenchymal stem cell VEGF production. J Mol Cell Cardiol 42:1009-15
Patel, Ketan M; Crisostomo, Paul; Lahm, Tim et al. (2007) Mesenchymal stem cells attenuate hypoxic pulmonary vasoconstriction by a paracrine mechanism. J Surg Res 143:281-5
Meldrum, K K; Misseri, R; Metcalfe, P et al. (2007) TNF-alpha neutralization ameliorates obstruction-induced renal fibrosis and dysfunction. Am J Physiol Regul Integr Comp Physiol 292:R1456-64
Meldrum, Kirstan K; Metcalfe, Peter; Leslie, Jeffrey A et al. (2006) TNF-alpha neutralization decreases nuclear factor-kappaB activation and apoptosis during renal obstruction. J Surg Res 131:182-8

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