Deficiency of developmental endothelial locus-1 (Del-1) aggravates bleomycin-induced pulmonary fibrosis in mice

YY Kang, DY Kim, SH Lee, EY Choi - Biochemical and Biophysical …, 2014 - Elsevier
YY Kang, DY Kim, SH Lee, EY Choi
Biochemical and Biophysical Research Communications, 2014Elsevier
Pulmonary fibrosis is a lung disease wherein lung parenchyma is gradually and irreversibly
replaced with collagen. The molecular pathogenesis of pulmonary fibrosis is not fully
understood and the only effective treatment available is lung transplantation. To test if Del-1,
an endogenous anti-inflammatory molecule, may be implicated in the development of
pulmonary fibrosis, we induced pulmonary fibrosis in wild type (WT) and Del-1−/− mice by
intratracheal administration of bleomycin. Del-1 expression in the lung was decreased in the …
Abstract
Pulmonary fibrosis is a lung disease wherein lung parenchyma is gradually and irreversibly replaced with collagen. The molecular pathogenesis of pulmonary fibrosis is not fully understood and the only effective treatment available is lung transplantation. To test if Del-1, an endogenous anti-inflammatory molecule, may be implicated in the development of pulmonary fibrosis, we induced pulmonary fibrosis in wild type (WT) and Del-1−/− mice by intratracheal administration of bleomycin. Del-1 expression in the lung was decreased in the WT mice treated with bleomycin compared to control mice. In addition, bleomycin-induced pulmonary fibrosis increased collagen deposition and TGF-β production in the lung of Del-1−/− mice. Finally, Del-1−/− mice treated with bleomycin displayed higher weight loss and greater mortality than did WT mice identically treated. These findings suggest that Del-1 may negatively regulate development of pulmonary fibrosis. Further delineation of a role for Del-1 in the development of pulmonary fibrosis will broaden our understanding of the molecular pathogenesis of this disease and hopefully help develop potential therapeutics.
Elsevier