
Idiopathic pulmonary fibrosis (IPF) is a poorly understood, progressive, lethal lung disease with no known cure. Recent work demonstrates that monocyte-derived alveolar macrophages (moAMs) drive lung fibrosis, but the further characterization of critical moAM cell attributes is necessary. This study shows that patients with IPF and mice with pulmonary fibrosis have increased expression of Heparin-binding epidermal growth factor-like growth factor (HB-EGF) and that lung macrophages and transitional AECs of mice with pulmonary fibrosis and humans all express HB-EGF.
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