Several studies by our lab and other groups at the Emory Alcohol and Lung Biology Center have shown that chronic ethanol abuse predisposes the lung to injury. We have identified Bronchiolitis Obliterans Syndrome (BOS) as another serious clinical condition that may be affected by chronic alcohol abuse. BOS is an airway obstruction disease that primarily affects lung transplant recipients, however it is also prevalent in patients who are exposed to particular toxins and infections. Compelling preliminary data show that chronic ethanol ingestion by donor rats exacerbates obliterative bronchiolitis (OB) in a rodent heterotopic tracheal transplant model. We propose that chronic alcohol abuse by transplant donors may predispose the donor lung to BOS by decreasing granulocyte/macrophage colony stimulating factor (GM-CSF)-mediated epithelial integrity via the TGFbeta1 signaling pathway. This is relevant in the context of lung transplantation as many organ donors are otherwise young healthy individuals who die in alcohol-related accidents. This proposal has three overall goals: (1) to determine the effect of donor ethanol ingestion on OB; (2) to investigate the role of GMCSF; and (3) to investigate the role of TGFbeta1 in the pathogenesis of experimental-induced OB.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AA016262-02
Application #
7277280
Study Section
Special Emphasis Panel (ZAA1-HH (52))
Program Officer
Gentry, Thomas
Project Start
2006-07-01
Project End
2008-03-31
Budget Start
2007-07-01
Budget End
2008-03-31
Support Year
2
Fiscal Year
2007
Total Cost
$39,042
Indirect Cost
Name
Emory University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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Pelaez, A; Force, S D; Gal, A A et al. (2010) Receptor for advanced glycation end products in donor lungs is associated with primary graft dysfunction after lung transplantation. Am J Transplant 10:900-7
Mitchell, Patrick O; Jensen, J Spencer; Ritzenthaler, Jeffrey D et al. (2009) Alcohol primes the airway for increased interleukin-13 signaling. Alcohol Clin Exp Res 33:505-13
Otis, Jeffrey S; Mitchell, Patrick O; Kershaw, Corey D et al. (2008) Na,K-ATPase expression is increased in the lungs of alcohol-fed rats. Alcohol Clin Exp Res 32:699-705
Mitchell, Patrick O; Guidot, David M (2007) Alcohol ingestion by donors amplifies experimental airway disease after heterotopic transplantation. Am J Respir Crit Care Med 176:1161-8