Journal Article

Mfge8 diminishes the severity of tissue fibrosis in mice by binding and targeting collagen for uptake by macrophages

Sheppard, Dean, Wolters, Paul, Emson, Claire L., Atabai, Kamran, Rahman, Salman, DeHart, Greg, Werb, Zena, Jame, Sina, Azhar, Nabil, Kuo, Alex, Lam, Michael, Turner, Scott M., McKleroy, William, Xia, Dee Dee, Melton, Andrew C.

2009

Overview

Milk fat globule epidermal growth factor 8 (Mfge8) is a soluble glycoprotein known to regulate inflammation and immunity by mediating apoptotic cell clearance. Since fibrosis can occur as a result of exaggerated apoptosis and inflammation, we set out to investigate the hypothesis that Mfge8 might negatively regulate tissue fibrosis. We report here that Mfge8 does decrease the severity of tissue fibrosis in a mouse model of pulmonary fibrosis; however, it does so not through effects on inflammation and apoptotic cell clearance, but by binding and targeting collagen for cellular uptake through its discoidin domains. Initial analysis revealed that Mfge8-/- mice exhibited enhanced pulmonary fibrosis after bleomycin-induced lung injury. However, they did not have increased inflammation or impaired apoptotic cell clearance after lung injury compared with Mfge8+/+ mice; rather, they had a defect in collagen turnover. Further experiments indicated that Mfge8 directly bound collagen and that Mfge8-/- macrophages exhibited defective collagen uptake that could be rescued by recombinant Mfge8 containing at least one discoidin domain. These data demonstrate a critical role for Mfge8 in decreasing the severity of murine tissue fibrosis by facilitating the removal of accumulated collagen.

• Publisher: American Society for Clinical Investigation
• Subject: Animals / Antibodies / Antigens, Surface - chemistry / Antigens, Surface - genetics / Antigens, Surface - metabolism / Apoptosis / Base Sequence / Biomedical research / Bleomycin - toxicity / Chemical properties / Collagen / Collagen - metabolism / Discoidins / Disease Models, Animal / DNA Primers - genetics / Epidermal growth factor / Extracellular matrix / Extracellular Matrix - metabolism / Female / Fibrosis / Glycoproteins / Inflammation / Lectins - chemistry / Lectins - genetics / Lungs / Macrophages / Macrophages, Alveolar - drug effects / Macrophages, Alveolar - metabolism / Macrophages, Alveolar - pathology / Male / Mice / Mice, Knockout / Milk Proteins - chemistry / Milk Proteins - genetics / Milk Proteins - metabolism / Protein Binding / Protein Structure, Tertiary / Proteins / Protozoan Proteins - chemistry / Protozoan Proteins - genetics / Pulmonary fibrosis / Pulmonary Fibrosis - chemically induced / Pulmonary Fibrosis - metabolism / Pulmonary Fibrosis - pathology / Recombinant Proteins - chemistry / Recombinant Proteins - genetics / Recombinant Proteins - metabolism / Targeting (Nuclear strategy)