? Based on new insights into the molecular processes of ALI we hypothesize that a longitudinal analysis of cells of innate immunity and thrombosis will demonstrate changes in RNA and protein expression that are significantly associated with progression of All from sepsis. Hypothesis 1: The progression of sepsis-induced ALI is significantly associated with critical interactions between Th1 and Th2 lymphocytes and platelets.
Specific Aim 1. We will collect total RNA from peripheral blood neutrophils, monocytes, TH1 and TH2 and CD8+ T lymphocytes and platelets from 20 mechanically ventilated pediatric patients with early ALI from sepsis. Blood sampling will take place at 6 individual time points over 72 hours along with severity of illness scoring to determine degree of disease progression. The temporal series of all 6 cell types banked for 3 retrospectively identified patients exemplary of ALI progression will be expression profiled and compared to profiles in 3 non-progressive ALI patients and 3 normal controls in order to generate a map of potential cell-cell interactions. Hypothesis 2: The pattern of peripheral blood cell expression of genes and proteins functionally important to the progression of ALI from sepsis will reflect the pattern of gene and protein expression in pulmonary edema cells and fluid.
Specific Aim 2. Using the prioritization model from Aim 1, we will select the 2 cell types that show promise as """"""""indicator"""""""" cell types. From the prospective cell collections in Aim 1 and more focused collections in this aim, we will choose, at random, 15 progressive and 15 non-progressive ALI subjects as determined by criteria outlined in the text of this proposal. We will verify select indicator gene expression changes found in Aim 1 by QMF RT-PCR in all 30 subjects (e.g. in the 20 genes with the most significant fold changes or most functional relevance.) Functionally important changes in gene expression will be confirmed in the entire cohort on the protein level by flow cytometry, and/or ELISA of proteins in peripheral blood and pulmonary edema fluid. ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Mentored Patient-Oriented Research Career Development Award (K23)
Project #
1K23RR020069-01A2
Application #
6928117
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Program Officer
Wilde, David B
Project Start
2005-09-23
Project End
2010-06-30
Budget Start
2005-09-23
Budget End
2006-06-30
Support Year
1
Fiscal Year
2005
Total Cost
$124,686
Indirect Cost
Name
Children's Research Institute
Department
Type
DUNS #
143983562
City
Washington
State
DC
Country
United States
Zip Code
20010
Mao, G F; Goldfinger, L E; Fan, D C et al. (2017) Dysregulation of PLDN (pallidin) is a mechanism for platelet dense granule deficiency in RUNX1 haplodeficiency. J Thromb Haemost 15:792-801
Sharron, Matthew; Hoptay, Claire E; Wiles, Andrew A et al. (2012) Platelets induce apoptosis during sepsis in a contact-dependent manner that is inhibited by GPIIb/IIIa blockade. PLoS One 7:e41549
Meyer, Andrew D; Wiles, Andrew A; Rivera, Oswaldo et al. (2012) Hemolytic and thrombocytopathic characteristics of extracorporeal membrane oxygenation systems at simulated flow rate for neonates. Pediatr Crit Care Med 13:e255-61
Iqbal, Sabah Fatima; Freishtat, Robert J (2011) Mechanism of action of vitamin D in the asthmatic lung. J Investig Med 59:1200-2
Freishtat, Robert J; Watson, Alan M; Benton, Angela S et al. (2011) Asthmatic airway epithelium is intrinsically inflammatory and mitotically dyssynchronous. Am J Respir Cell Mol Biol 44:863-9
Pillai, Dinesh K; Iqbal, Sabah F; Benton, Angela S et al. (2011) Associations between genetic variants in vitamin D metabolism and asthma characteristics in young African Americans: a pilot study. J Investig Med 59:938-46
Stemmy, Erik J; Benton, Angela S; Lerner, Jennifer et al. (2011) Extracellular cyclophilin levels associate with parameters of asthma in phenotypic clusters. J Asthma 48:986-993
Watson, Alan M; Benton, Angela S; Rose, Mary C et al. (2010) Cigarette smoke alters tissue inhibitor of metalloproteinase 1 and matrix metalloproteinase 9 levels in the basolateral secretions of human asthmatic bronchial epithelium in vitro. J Investig Med 58:725-9
Benton, Angela S; Kumar, Nikila; Lerner, Jennifer et al. (2010) Airway platelet activation is associated with airway eosinophilic inflammation in asthma. J Investig Med 58:987-90
Freishtat, Robert J; Nagaraju, Kanneboyina; Jusko, William et al. (2010) Glucocorticoid efficacy in asthma: is improved tissue remodeling upstream of anti-inflammation. J Investig Med 58:19-22

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