| First Author | Guzy RD | Year | 2017 |
| Journal | J Biol Chem | Volume | 292 |
| Issue | 25 | Pages | 10364-10378 |
| PubMed ID | 28487375 | Mgi Jnum | J:245966 |
| Mgi Id | MGI:5916500 | Doi | 10.1074/jbc.M117.791764 |
| Citation | Guzy RD, et al. (2017) Pulmonary fibrosis requires cell-autonomous mesenchymal fibroblast growth factor (FGF) signaling. J Biol Chem 292(25):10364-10378 |
| abstractText | Idiopathic pulmonary fibrosis (IPF) is characterized by progressive pulmonary scarring, decline in lung function, and often results in death within 3-5 five years after diagnosis. Fibroblast growth factor (FGF) signaling has been implicated in the pathogenesis of IPF; however, the mechanism through which FGF signaling contributes to pulmonary fibrosis remains unclear. We hypothesized that FGF receptor (FGFR) signaling in fibroblasts is required for the fibrotic response to bleomycin. To test this, mice with mesenchyme-specific tamoxifen-inducible inactivation of FGF receptors 1, 2, and 3 (Col1alpha2-CreER; TCKO mice) were lineage labeled and administered intratracheal bleomycin. Lungs were collected for histologic analysis, whole lung RNA and protein, and dissociated for flow cytometry and FACS. Bleomycin-treated Col1alpha2-CreER; TCKO mice have decreased pulmonary fibrosis, collagen production, and fewer alpha-smooth muscle actin-positive (alphaSMA+) myofibroblasts compared with controls. Freshly isolated Col1alpha2-CreER; TCKO mesenchymal cells from bleomycin-treated mice have decreased collagen expression compared with wild type mesenchymal cells. Furthermore, lineage labeled FGFR-deficient fibroblasts have decreased enrichment in fibrotic areas and decreased proliferation. These data identify a cell autonomous requirement for mesenchymal FGFR signaling in the development of pulmonary fibrosis, and for the enrichment of the Col1alpha2-CreER-positive (Col1alpha2+) mesenchymal lineage in fibrotic tissue following bleomycin exposure. We conclude that mesenchymal FGF signaling is required for the development of pulmonary fibrosis, and that therapeutic strategies aimed directly at mesenchymal FGF signaling could be beneficial in the treatment of IPF. |
