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This program will identify mechanisms underlying fibroblast activation that accumulate in the distal areas of IPF lungs using four projects with a synergistic focus on 1) WT1-driven novel targets underlying fibroblast activation, 2) Inhibition of WT1-MYCN-PLK1 axis and pulmonary fibrosis using PLK1-specific inhibitor, volasertib, 3) Role of Sox9 in basal cell and fibroblasts dysfunction in IPF lungs, and 4) therapeutic inhibition of Sox9 expression to attenuate pulmonary fibrosis.
This program will identify cellular and molecular mechanisms underlying airway inflammation and smooth muscle cell contraction in the pathogenesis of asthma. The schemata below highlight how Th1 and Th2 cytokines regulate IL-31RA to alter smooth muscle cell contraction and AHR in asthma.
University of CincinnatiDepartment of Internal Medicine Division of Pulmonary, Critical Care, and Sleep Medicine 231 Albert Sabin Way, ML 0564 Cincinnati, OH 45267-0564
Phone: 513-558-4831 Fax: 513-558-4858 Email: pulmonary@uc.edu