This Program Project Grant application is founded on the hypothesis that during lung injury, recovery of alveolar epithelial cell function is of crucial importance in the prevention of disordered healing, fibrosis and thus the outcome of patients with the acute respiratory distress syndrome (ARDS). We have assembled a highly interactive group of investigators who have worked collaboratively, productively and synergistically in the previous cycle of the grant. We propose to study alveolar epithelial cell injury and repair via three interrelated projects and three supportive cores. In Project # 1 we will focus on the mechanisms regulating alveolar epithelial function during hypoxia as it pertains to Na,K-ATPase phosphorylation-endocytosis and ubiquitination-degradation. In Project # 2 we will determine the role of intermediate filaments in alveolar epithelial wound repair and remodeling. In Project # 3 we will investigate the mechanisms of alveolar epithelial apoptosis in the development of lung injury and repair. Collaborative studies have been conducted for each of the projects and the preliminary results support the feasibility of this proposal. This Program Project focuses the multidisciplinary expertise of the investigators on the elucidation of mechanisms contributing to lung epithelial cell injury in clinically relevant models of injury. These projects are interactive conceptually and programmatically, where the aggregate of the projects is greater than the sum of its parts. Their collective outcome will provide a composite picture of the regulation of the Na,K-ATPase and intermediate filaments in the alveolar epithelium during injury and determine the role of alveolar epithelial cell apoptosis in the pathogenesis of lung injury. The insights gained from the data generated from these studies will provide novel molecular targets for the development of new therapeutic strategies to treat patients with lung injury.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
Research Program Projects (P01)
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Application #
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Program Officer
Harabin, Andrea L
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Northwestern University at Chicago
Internal Medicine/Medicine
Schools of Medicine
United States
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Sala, Marc A; Balderas-Martínez, Yalbi Itzel; Buendía-Roldan, Ivette et al. (2018) Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosis. Respir Res 19:233
Mehta, Manan M; Weinberg, Samuel E; Steinert, Elizabeth M et al. (2018) Hexokinase 2 is dispensable for T cell-dependent immunity. Cancer Metab 6:10
Brazee, Patricia L; Dada, Laura A (2018) Splice Wars: The Role of MLCK Isoforms in Ventilation-induced Lung Injury. Am J Respir Cell Mol Biol 58:549-550
Koch, Clarissa M; Chiu, Stephen F; Akbarpour, Mahzad et al. (2018) A Beginner's Guide to Analysis of RNA Sequencing Data. Am J Respir Cell Mol Biol 59:145-157
Dela Cruz, Charles S; Wunderink, Richard G; Christiani, David C et al. (2018) Future Research Directions in Pneumonia. NHLBI Working Group Report. Am J Respir Crit Care Med 198:256-263
Kong, Hyewon; Chandel, Navdeep S (2018) Regulation of redox balance in cancer and T cells. J Biol Chem 293:7499-7507
Hsiao, Hsi-Min; Fernandez, Ramiro; Tanaka, Satona et al. (2018) Spleen-derived classical monocytes mediate lung ischemia-reperfusion injury through IL-1?. J Clin Invest 128:2833-2847
Wang, Zheng; Divanyan, Alex; Jourd'heuil, Frances L et al. (2018) Vimentin expression is required for the development of EMT-related renal fibrosis following unilateral ureteral obstruction in mice. Am J Physiol Renal Physiol 315:F769-F780
Lu, Ziyan; Casalino-Matsuda, S Marina; Nair, Aisha et al. (2018) A role for heat shock factor 1 in hypercapnia-induced inhibition of inflammatory cytokine expression. FASEB J 32:3614-3622
Amarelle, Luciano; Lecuona, Emilia (2018) A Nonhospitable Host: Targeting Cellular Factors as an Antiviral Strategy for Respiratory Viruses. Am J Respir Cell Mol Biol 59:666-667

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